Research | Open | Published:
HE4 promotes collateral resistance to cisplatin and paclitaxel in ovarian cancer cells
Journal of Ovarian Researchvolume 9, Article number: 28 (2016)
Chemotherapy resistance presents a difficult challenge in treating epithelial ovarian cancer patients, particularly when tumors exhibit resistance to multiple chemotherapeutic agents. A few studies have shown that elevated serum levels of the ovarian cancer biomarker HE4 correlate with tumor chemoresistance, response to treatment, and survival. Here, we sought to confirm our previous results that HE4 contributes to collateral resistance to cisplatin and paclitaxel in vitro and uncover factors that may contribute to HE4-mediated chemoresistance.
MTS assays and western blots for cleaved PARP were used to assess resistance of HE4-overexpressing SKOV3 and OVCAR8 clones to cisplatin and paclitaxel. CRISPR/Cas technology was used to knockdown HE4 in HE4-overexpressing SKOV3 cells. A microarray was conducted to determine differential gene expression between SKOV3 null vector-transfected and HE4-overexpressing clones upon cisplatin exposure, and results were validated by quantitative RT-PCR. Regulation of mitogen activated protein kinases (MAPKs) and tubulins were assessed by western blot.
HE4-overexpressing SKOV3 and OVCAR8 clones displayed increased resistance to cisplatin and paclitaxel. Knockdown of HE4 in HE4-overexpressing SKOV3 cells partially reversed chemoresistance. Microarray analysis revealed that HE4 overexpression resulted in suppression of cisplatin-mediated upregulation of EGR1, a MAPK-regulated gene involved in promoting apoptosis. Upregulation of p38, a MAPK activated in response to cisplatin, was suppressed in HE4-overexpressing clones. No differences in extracellular signal-regulated kinase (ERK) activation were noted in HE4-overexpressing clones treated with 25 μM cisplatin, but ERK activation was partially suppressed in HE4-overexpressing clones treated with 80 μM cisplatin. Furthermore, treatment of cells with recombinant HE4 dramatically affected ERK activation in SKOV3 and OVCAR8 wild type cells. Recombinant HE4 also upregulated α-tubulin and β-tubulin levels in SKOV3 and OVCAR8 cells, and microtubule associated protein tau (MAPT) gene expression was increased in SKOV3 HE4-overexpressing clones.
Overexpression of HE4 promotes collateral resistance to cisplatin and paclitaxel, and downregulation of HE4 partially reverses this chemoresistance. Multiple factors could be involved in HE4-mediated chemoresistance, including deregulation of MAPK signaling, as well as alterations in tubulin levels or stability.
Chemotherapy resistance is a challenging problem in the treatment of epithelial ovarian cancer (EOC) patients. While a majority (80 %) of women initially responds to first-line platinum/taxane chemotherapy, recurrent disease presents in 60–85 % of patients, and is fundamentally incurable [1, 2]. However, patients with recurrent disease that is platinum-sensitive have a better response rate and improved progression free survival (PFS) and overall survival (OS) when treated with combination therapy . In patients with platinum-resistant disease, single agent paclitaxel was shown to produce an objective response rate of only 22–30 % . In the case of patients with disease that is resistant to both platinum and paclitaxel, other options are available, such as pegylated liposomal doxorubicin (PLD), topotecan, and gemcitabine ; however, it is not always clear which patients may benefit most from each therapy. Ultimately, although multidrug regimens are associated with higher toxicity, they are more effective than single agent therapies. Gaining a better understanding of factors contributing to resistance to platinum and taxane based therapies will be valuable in guiding treatment decisions for ovarian cancer patients.
Human epididymis protein-4 (HE4/WFDC2) is a small secretory protein that belongs to the family of whey acidic protein (WAP) domain-containing anti-proteases , and has been shown to possess cross-class anti-protease activity itself . It is overexpressed in ovarian cancer tissues compared to normal ovaries, and has been identified as a novel biomarker for EOC [5, 6]. Serum levels predict ovarian cancer with equivalent sensitivity to CA125, but with the advantage that HE4 is less frequently elevated in patients with benign gynecological conditions . A multicenter study led by our institution established a new algorithm for the diagnosis of women with an ovarian mass . The FDA-approved Risk of Ovarian Malignancy Algorithm (ROMA) uses HE4 along with CA125 and menopausal status to predict a woman’s risk of ovarian cancer and monitor disease with improved sensitivity and specificity over the Risk of Malignancy Index (RMI) that used CA125, pelvic sonography, and menopausal status .
Recently, HE4 has been associated with the development of chemoresistance clinically. We have previously determined that HE4 and ROMA scores are more sensitive predictors of platinum response than CA125 alone . Angioli et al. reported that serum HE4 levels predict platinum-resistant versus sensitive disease at the third chemotherapy cycle with 100 % sensitivity and 85 % specificity . Similarly, another study found that serum HE4 concentration is higher in patients resistant to first-line chemotherapy . Among high-grade serous ovarian cancer (HGSC) patients, those whose HE4 levels displayed greater reduction during neoadjuvant chemotherapy had improved OS . Collectively, these studies point to HE4 as a predictor of chemotherapy response/resistance, but do not address the question of whether HE4 has a causative role in the development of resistance.
We have also shown that SKOV3 ovarian cancer cells overexpressing HE4 are more resistant to cisplatin and paclitaxel, while HE4-overexpressing OVCAR8 ovarian cancer cells exhibit greater cisplatin resistance than their null vector-transfected counterparts . In mice, SKOV3 xenografts overexpressing HE4 also grew larger than control SKOV3 xenografts . In support of these data, Wang et al. found that recombinant HE4-treated SKOV3 cells display reduced carboplatin-induced apoptosis, a decreased ratio of BAX/BCL2, and an overall downregulation of genes involved in DNA damage response and apoptosis . However, much remains to be elucidated regarding how HE4 promotes resistance to platinum or taxane therapies. Therefore, we sought first to confirm our preliminary studies suggesting a causative role for HE4 in cisplatin and paclitaxel resistance. Our second goal was to examine the gene expression profile of SKOV3 cells overexpressing HE4, as well as determine differences in regulation of gene expression in response to cisplatin treatment. Herein, we also begin to explore a few of the multifold processes that may contribute to HE4-mediated chemoresistance.
SKOV3 and OVCAR8 ovarian cancer cells were obtained from American Type Culture Collection (Manassas, VA). Cells were cultured in Dulbecco Modified Eagle Medium (DMEM, Gibco, 11965-065) with 10 % fetal bovine serum (FBS) and 1 % penicillin/streptomycin and kept in a 37 °C humidified incubator with 5 % CO2.
Stable cell lines
All null vector (NV) and HE4-overexpressing stable cell lines were previously established . To generate HE4-CRISPR Double Nickase stable cell lines, SKOV3-C1 cells were transfected in 6-well plates with 1 μg HE4 Double Nickase Plasmid (Santa Cruz, sc-402876-NIC) or Control Double Nickase Plasmid (Santa Cruz, sc-437281), using 5 μl Lipofectamine 2000 (Invitrogen). After 48 h, media was changed to 1 μg/ml puromycin containing media for five days, then split into larger plates and selected for an additional five days. RNA and tissue culture supernatant was collected to confirm downregulation of HE4 levels by quantitative RT-PCR (qRT-PCR) and ELISA. Cells were maintained in DMEM supplemented with 10 % FBS, 1 % penicillin/streptomycin, and 1 μg/ml puromycin.
Cells were treated with the described doses of cis-diamminedichloroplatinum(II) (cisplatin, Sigma Aldrich, 1134357) or paclitaxel (Sigma Aldrich, T7402) dissolved in dimethyl sulfoxide (DMSO, Sigma Aldrich, D8418), or DMSO alone as a control. Cells were collected directly into either Trizol (Ambion, 15596018) or Cell Lysis Buffer (Cell Signaling, 9803) at the indicated time points for analysis. Cells were treated with recombinant human HE4 (rHE4, MyBioSource, MBS355616) added directly to the media to a final concentration of 20 nM. Cells were treated with recombinant human epidermal growth factor (rEGF, Calbiochem, 324831) at a concentration of 10 ng/ml.
Cell viability assays
All cells were seeded at 2 000 cells/well in 96-well plates. Cells were treated with increasing doses of cisplatin and paclitaxel as described. After 48 h, cell viability assays were performed by adding 10 μl/well of CellTiter 96® Aqueous One Solution Cell Proliferation MTS Assay (Promega, G3580), incubating at 37 °C/5 % CO2 for 2 h, and reading absorbance at 492 nm. Results are displayed as percent survival of vehicle treated cells.
SKOV3-NV and SKOV3-C1 cells were treated in triplicate at 80 % confluency with 25 μM cisplatin or DMSO vehicle. Total RNA was collected 24 h later using an RNeasy Mini Kit (Qiagen, 74104) and checked for purity by NanoDrop 2000 (Thermo Scientific). The RNA samples were randomly assigned numbers and submitted to the Brown Genomics Core Facility for Bioanalyzer (Agilent 2100) RNA quality analysis. Affymetrix HTA 2.0 Arrays were performed according to the manufacturer’s instructions at the Core Facility using 150 ng total input RNA.
Database for Annotation, Visualization, and Integrated Discovery (DAVID) v6.7 [12, 13] was used to identify the top ten enriched annotation terms among 180 genes differentially expressed (1.5-fold in either direction, p < .05) between SKOV3-NV and SKOV3-C1. Default DAVID parameters were employed as follows:
Kappa Similarity: Similarity Term Overlap – 3; Similarity Threshold – 0.5
Classification: Initial Group Membership – 3; Final Group Membership – 3; Multiple Linkage Threshold – 0.5
Enrichment Threshold: EASE – 1.0
RNA was collected using an RNeasy Mini Kit (Qiagen, 74104) or Trizol extraction/LiCl precipication. Total RNA (500 ng) was reverse transcribed into cDNA using the iScript cDNA Synthesis Kit (Bio-Rad, 1708890) according the manufacturer’s protocol. To validate differentially expressed genes between SKOV3-NV and SKOV3-C1 cells identified by microarray, the same RNA samples used for the microarray were employed. To validate the differential cisplatin-induced upregulation of EGR1 between SKOV3-NV and SKOV3-C1/C7, microarray RNA samples were used, as well as RNA isolated from SKOV3-C7 cells that were treated in the same manner as the cells used in the microarray. Quantitative PCR was performed in triplicate by loading 1 μl cDNA reaction, 2 μl each of 5 μM custom forward and reverse primers (Invitrogen) or 1 μM forward and reverse validated primers (realtimeprimers.com), 10 μl SYBR Green (Applied Biosciences [ABI], 4367659) and 5 μl RNAse-free water to each well. Samples were run on an ABI 7500 Fast Real-Time PCR System, and data was analyzed using the ΔΔCt method. Relative expression levels were normalized to 18 s rRNA to correct for equivalent total RNA levels. Validated MAPT, CYP1B1, and EGR1 primers were purchased from realtimeprimers.com. Custom primer sequences (Invitrogen) are as follows:
AKT3 F – AAG GGA AGA ATG GAC AGA
AKT3 R – ATG GGT TGT AGA GGC ATC
NMUR2 F – CCG TTC CAC ATT GAC CGA CT
NMUR2 R – CAC CAC ATG GAC GAG GTT GA
SEPT3 F – TTG CCC TGC TTC GAG ACT TT
SEPT3 R – CTT TCC TCT GTG TCC ACG CT
18 s rRNA F – CCG CGG TTC TAT TTT GTT GG
18 s rRNA R – GGC GCT CCC TCT TAA TCA TG
Protein was extracted from cell pellets in Cell Lysis Buffer (Cell Signaling, 9803) with 1 mM PMSF, according to the manufacturer’s protocol. Protein concentrations were determined by DC Protein Assay (Bio-Rad Laboratories, 5000116). Western blot analysis was performed by loading equal amounts of protein boiled with Novex Sample Reducing Agent (Life Technologies, NP009) and NuPAGE LDS sample buffer (ThermoFisher Scientific, NP0007) into a 4–12 % gradient NuPAGE Novex Bis-Tris gel [Life Technologies, NP0321BOX (mini), WG1402BX10 (midi)]. Protein was transferred by semi-dry transfer to methanol-activated 0.2 μm PVDF membranes (Bio-Rad, 162-0177) at 0.12-0.2 A for 1 h 15 m. Membranes were blocked in 5 % milk in phosphate-buffered saline with 0.05 % Tween 20 (PBS-T) for 30 m at room temperature, incubated in primary antibody in 5 % milk in PBS-T overnight at 4 °C, and then in secondary antibody in 5 % milk in PBS-T for 1 h at room temperature, with PBS-T washes in between. Amersham ECL Prime Western Blot Detection System (GE Healthcare, RPN2232) was used for detection of HRP-tagged secondary antibodies. Blots were developed using x-ray film in a Kodac film developer or imaged directly in a Biorad Chemidoc MP Imaging System. GAPDH was used as a loading control. Antibodies and dilutions used are as follows:
PARP (Cell Signaling, 9532, 1:1000)
phospho-p44/42 MAPK (ERK1/2) (Cell Signaling, 4370, 1:2000)
p44/42 (ERK1/2) (Cell Signaling, 9102, 1:2000)
EGR1 (Santa Cruz, sc-110, 1:200)
p38 (Cell Signaling, 9212, 1:1000)
phospho-p38 (Cell Signaling, 9215, 1:1000)
GAPDH (Cell Signaling, 2118, 1:2000)
β-tubulin (Cell Signaling, 2146, 1:2000)
α-tubulin (Cell Signaling, 2144, 1:1000)
Image J was used to perform densitometry analysis of western blots. Images of blots were analyzed in 8-bit TIFF format, using the “analyze gel” function. Where no band was detected, a value of “1” was assigned. Relative band densities were normalized to a loading control, or the appropriate total protein for phospho-proteins, and then the lowest value was set to 1.
In all instances where statistics are shown, they represent n ≥ 3 independent experiments, and p-values were determined by unpaired 2-tailed Student t-test. For the microarray, Affymetrix Transcriptome Analysis Console (TAC) software was used to generate fold-changes and statistical significance, and ANOVA p-values generated by TAC were used for p-value cutoffs.
HE4-overexpressing cells are more resistant to cisplatin and paclitaxel treatment
Since HE4 serum levels correlate with cisplatin resistance in ovarian cancer patients [7–10], and our previous data suggested that HE4 promotes chemotherapy resistance in vitro and in vivo , we set out to further define the chemotherapy response of ovarian cancer cells that overexpress HE4. We employed SKOV3 ovarian cancer cells stably expressing a null vector plasmid (SKOV3-NV) and two different clonally-selected cell lines stably expressing a pCMV6-HE4 plasmid (SKOV3-C1 and SKOV3-C7) . SKOV3 cells are ideal to examine the effects of HE4 overexpression since they secrete very low levels of HE4 (<15 pM), as detected by ELISA . We treated the cells with 0, 1.56, 3.125, 6.25, and 12.5 μM cisplatin or 0, 0.625, 1.25, 2.5, and 5 nM paclitaxel for 48 h, then performed MTS assays to measure cell viability. SKOV3-C1 and SKOV3-C7 cells were significantly more resistant than SKOV3-NV cells to cisplatin (Fig. 1a) at 3.125 μM (p = .029 and .024, respectively), 6.25 μM (p = .034 and 0.37, respectively), and 12.5 μM (p = .0020 and .0018, respectively). SKOV3-C1 and SKOV3-C7 cells were also more resistant than SKOV3-NV cells to paclitaxel (Fig. 1b) at 1.25 nM (p = .017 and .083, respectively), 2.5 nM (p = .0094 and .022, respectively) and 5 nM (p = .0050 and .0035, respectively).
In order to confirm that this resistance was due to inhibition in apoptosis, we analyzed the cleavage of poly ADP ribose polymerase (PARP) in SKOV3-NV, SKOV3-C1, and SKOV3-C7 cells treated with 5 μM cisplatin for 24, 48, and 72 h. Even in untreated cells, baseline levels of cleaved PARP were lower in HE4-overexpressing clones than in SKOV3-NV cells. In SKOV3-NV cells, PARP cleavage was clearly increased by 5 μM cisplatin at 24 h, and continued to remain elevated at 48 h. By 72 h, levels of cleaved PARP had diminished in SKOV3-NV cells, presumably because most of the cells had already undergone apoptosis. In HE4-overexpressing clones, uncleaved PARP did accumulate to a similar degree as in SKOV3-NV cells—suggesting that the cisplatin was able to enter the cells and cause DNA damage, thus recruiting PARP to sites of single-strand breaks. However, cleavage of PARP did not occur in HE4-overexpressing cells, indicating that the process of apoptosis was not completed (Fig. 1c-d). We also observed an accumulation in both PARP and cleaved PARP in SKOV3-NV cells treated with 1 nM paclitaxel for 48 h, but did not see this response as strongly in SKOV3-C1 or SKOV3-C7 cells (Fig. 1e-f). The fact that PARP did not accumulate robustly in HE4-overexpressing clones treated with paclitaxel—unlike what we saw with cisplatin treatment—is likely due to the vastly different mechanisms of action by which these two drugs result in DNA damage.
Preliminary dose response experiments revealed that OVCAR8 cells required high doses of cisplatin to achieve cell death. Thus, we treated OVCAR8-NV and HE4-overexpressing clones (OVCAR8-C5) with 0, 62.5, 125, 250, and 500 μM cisplatin for 24 h, and found a slight increase in resistance in the OVCAR8-C5 cells (Additional file 1A), which was also reflected by lower levels of cleaved PARP in OVCAR8-C5 cells than OVCAR8-NV cells treated with 100 μM cisplatin for 24 h (Additional file 1B-C). However, although OVCAR8 cells also secrete undetectable levels of HE4 as determined by ELISA (data not shown), they appear to already be highly resistant to cisplatin and are not an ideal model to examine the effects of HE4 on chemotherapy resistance. Likewise, OVCAR8-NV cells were also more resistant to paclitaxel than SKOV3-NV cells, and only exhibited a modest increase in resistance with HE4 overexpression (Additional file 1D). For this reason, we focused primarily on SKOV3 cells for the remainder of our studies.
CRISPR/Cas-mediated HE4 downregulation reduces chemoresistance in SKOV3-C1 cells
In order to confirm that overexpression of HE4 was responsible for the increase in cisplatin resistance observed, we knocked down HE4 in SKOV3-C1 cells by stable transfection of a human HE4 CRISPR/Cas Double Nickase plasmid. RNA from HE4-targeted cells (CRISPR-HE4) and control plasmid transfected cells (CRISPR-Ctrl) was collected to confirm effective targeting of the HE4 gene. Cell culture supernatant was also collected and subjected to ELISA to determine levels of secreted HE4 in the media. CRISPR-HE4 transfected cells displayed 70.3 % knockdown (p = .02) in HE4 mRNA levels compared to control cells. Furthermore, CRISPR-HE4 media had undetectable levels (<15 pM) of HE4, which is in agreement with what we previously observed in SKOV3 wild type and SKOV3-NV cells. HE4 concentration in CRISPR-Ctrl media measured 307 pM, which was comparable to our previously reported levels for SKOV3-C1 and SKOV3-C7 cells (250 pM and 362 pM, respectively)  (Fig. 2a). Next, we measured survival of CRISPR-Ctrl and CRISPR-HE4 cells in response to 25 μM cisplatin treatment (24 h), and found that CRISPR-Ctrl cells exhibited 92.2 % cell survival compared to vehicle-treated cells, while CRISPR-HE4 cells displayed 81.9 % survival compared to vehicle-treated cells (p = .005; Fig. 2b). Likewise, CRISPR-Ctrl cells exhibited 73.9 % survival in response to paclitaxel versus 65.9 % survival of CRISPR-HE4 cells (p = .005) (Fig. 2c).
Microarray analysis reveals genes differentially regulated by HE4 in ovarian cancer cells
In order to gain a better understanding of the differential regulation of transcription between SKOV3-NV and SKOV3-C1 cells in the presence and absence of cisplatin, we performed a microarray analysis of total RNA collected from SKOV3-NV and SKOV3-C1 cells treated with either vehicle [dimethylsulfoxide (DMSO)] or 25 μM cisplatin for 24 h (n = 3/group). All transcripts differentially regulated between groups 1.5-fold in either direction (ANOVA p-value < .05) are available in Additional file 2. The top fifteen annotated, protein-coding genes that were differentially regulated in vehicle-treated SKOV3-C1 cells compared to SKOV3-NV (p < .05) are shown in Table 1. The Database for Annotation, Visualization and Integrated Discovery (DAVID) [12, 13] was used to perform gene ontology analysis of all genes differentially expressed 1.5-fold in either direction (p < .05) in SKOV3-C1 cells versus SKOV3-NV. This analysis revealed enrichment for the terms “secreted glycoproteins”, “transmembrane domains”, “pregnancy and immunoglobulin-like domains”, “cell adhesion”, “plasma membrane”, “fibronectin”, “insulin-like growth factor binding”, “membrane fraction”, “extracellular matrix”, and “EGF-like domains” (Additional file 3). We validated four of the genes from the list of most differentially expressed genes by quantitative reverse-transcription PCR (qRT-PCR), as follows: V-Akt Murine Thymoma Viral Oncogene Homolog 3 (AKT3); septin 3 (SEPT3); cytochrome p450, family 1, subfamily B, polypeptide 1 (CYP1B1); and neuromedin 2 (NMUR2) (Fig. 3a-b).
Cisplatin-induced upregulation of EGR1 is suppressed in HE4-overexpressing cells
The top fifteen annotated, protein-coding genes that were differentially regulated between SKOV3-NV and SKOV3-C1 cells in the presence of cisplatin are listed in Table 2. This list excludes genes that were already differentially regulated between SKOV3-NV and SKOV3-C1 vehicle treated cells. Of these genes, early growth response 1 (EGR1), which is a key gene involved in regulating growth and apoptosis in a wide variety of tissues, presented as the most differentially expressed, with 4.07-fold higher expression in SKOV3-NV than SKOV3-C1 (p = .000201). Silencing of EGR1 has been shown to promote resistance to cisplatin in esophageal cancer cells , while overexpression of this gene sensitizes ovarian cancer cells to cisplatin-induced apoptosis . Thus, we speculate that suppression of EGR1 upregulation serves as a downstream effector of HE4-mediated cisplatin resistance.
To further analyze genome-wide differences in cisplatin response between SKOV3-NV and SKOV3-C1 cells, we also conducted the following comparisons: SKOV3-NV (vehicle vs. cisplatin) and SKOV3-C1 (vehicle vs. cisplatin). The top fifteen differentially expressed annotated, protein-coding genes in either direction are displayed in Table 3. We also included EGR1 in this table, since it just missed the cutoff as the sixteenth gene upregulated in SKOV3-NV cells by cisplatin, but not in SKOV3-C1. Several other genes are represented in both Tables 2 and 3, including snail family zinc finger 1, (SNAI1), DNA-damage-inducible transcript 3 (DDIT3), ADP-ribosylation factor-like 14 (ARL14), and tumor necrosis factor (TNF). Moreover, while there were several genes that were cisplatin-regulated in both SKOV3-NV and SKOV3-C1, the overall number of all transcripts regulated by cisplatin (+/- 1.5-fold, p < .05) in SKOV3-NV was much greater than in SKOV3-C1 cells (5935 vs. 1035), as represented by comparative scatter plots (Additional file 4). Even among those genes that were regulated in both SKOV3-NV and SKOV3-C1 in Table 3, there tended to be a greater degree of change in SKOV3-NV cells, especially for those genes that were upregulated by cisplatin. These observations are in agreement with the stronger cisplatin-response in SKOV3-NV cells.
Because EGR1 was most the differentially expressed gene between SKOV3-NV and SKOV3-C1 treated with cisplatin, and has known roles in cisplatin response, we validated its differential regulation by qRT-PCR using SKOV3-NV, SKOV3-C1, and SKOV3-C7 RNA exposed to vehicle (DMSO) or 25 μM cisplatin for 24 h (Fig. 4a). Next, because EGR1 is an early response gene reported to be upregulated as early as 15–30 min following exposure to a stimulant [16, 17], we performed a time course analysis of EGR1 expression following cisplatin treatment of SKOV3-NV and SKOV3-C1 cells. Interestingly, an early upregulation of EGR1 occurred in both SKOV3-NV and SKOV3-C1 cells beginning at 15 min after cisplatin treatment, which peaked between 1 and 3 h post-treatment and diminished by 6 h. However, the second more robust increase in EGR1 expression observed at 24 h in SKOV3-NV cells was dramatically suppressed in SKOV3-C1 cells (Fig. 4b). A similar trend was noted in EGR1 protein levels. While EGR1 protein was increased at 6 h in both SKOV3-NV and SKOV3-C1 cells treated with 25 μM cisplatin, only SKOV3-NV cells maintained higher levels of EGR1 by 24 h (Fig. 4c-d). To confirm the intrinsic ability of SKOV3-C1 cells to upregulate EGR1, both SKOV3-NV and SKOV-C1 cells were treated with 10 ng/ml human recombinant epidermal growth factor (rEGF) to activate the EGFR signaling pathway, a known positive regulator of EGR1 gene expression [18, 19]. We observed a robust increase in EGR1 at 1 h after treatment in both SKOV3-NV and SKOV3-C1 cells (Fig. 4c-d), which is in agreement with a previous study using the same dose and time point . These data indicate that HE4-overexpressing cells are capable of upregulating EGR1, but some mechanism is activated to suppress its later upregulation in response to cisplatin. Activation of ERK in response to cisplatin and rEGF was comparable between SKOV3-NV and SKOV3-C1 cells (Fig. 4c and e).
HE4 promotes deregulation of mitogen activated protein kinase (MAPK) signaling
Because MAPKs transcriptionally activate EGR1 expression by phosphorylating the EGR1 transcription factor ELK-1 [19–21], we assessed levels of phosphorylated extracellular signal-regulated kinase (ERK) in SKOV3-NV, SKOV3-C1, SKOV3-C7, OVCAR8-NV, and OVCAR8-C5 cell lines, and observed that levels of phospho-ERK were higher in SKOV3 and OVCAR8 HE4-overexpressing clones than in SKOV3-NV cells (Fig. 5a-b). In addition, when SKOV3 wild type (WT) and OVCAR8-WT cells were treated with 20 nM human recombinant HE4 (rHE4) protein, levels of phospho-ERK were dramatically affected (Fig. 5c-d). In SKOV3-WT cells, phospho-ERK was almost completely obliterated as early as 1 h after treatment, but levels were restored to above baseline by 24 h. Conversely, phospho-ERK continuously increased from 1 h to 24 h in OVCAR8-WT cells. These differential results between SKOV3 and OVCAR8 cells suggest time-dependent and cell type-specific effects of HE4 on growth factor signaling, but highlight the fact that HE4 has a rapid and dramatic effect on kinase activation, which could in turn affect regulation of EGR1 in response to cisplatin.
Although we see a significant effect of rHE4 on phospho-ERK levels, we were unable to detect differences in ERK activation between SKOV3-NV and SKOV3-C1 in response to 6 h cisplatin treatment, as previously shown. Moreover, by 24 h (the timepoint where we see the greatest rise in EGR1), phospho-ERK levels are diminished in both SKOV3-NV and SKOV3-C1 cells (Fig. 4c and e). Since p38—another MAPK known to regulate EGR1 transcription —is also a key player in promoting apoptosis in response to cisplatin, we examined levels of phospho-p38 in SKOV3-NV and SKOV3-C1 clones following treatment with 25 μM cisplatin for 1, 6, and 24 h. Interestingly, p38 was robustly activated at 24 h in SKOV3-NV cells following cisplatin treatment, but this response was blunted in SKOV3-C1 cells (Fig. 5e-f). We also observed similar results comparing p38 activation in SKOV3-NV, SKOV3-C1, and SKOV3-C7 cells using a higher dose of cisplatin (80 μM), with robust activation noted at 6 h only in SKOV3-NV cells (Additional file 5A and B). We did observe a small suppression of ERK activation beginning at 1 h in HE4-overexpressing SKOV3 clones treated with this high dose of cisplatin, which was most apparent at 6 h after treatment, suggesting there may be subtle differences in how ERK is activated in HE4-overexpressing clones that only become apparent with high dose treatment (Additional file 5A and C).
HE4 modulates tubulin levels and MAPT gene expression
One of the genes we found to be differentially expressed between SKOV3-NV and SKOV3-C1 (vehicle treated) in our microarray analysis was microtubule associated protein tau (MAPT). MAPT, which is associated with paclitaxel resistance in several cancers including EOC [22–28], was more highly expressed in SKOV3-C1 cells than in SKOV3-NV cells (2.47-fold, p = .00702) (Additional file 2). We validated these results by qPCR, finding 4.42-fold higher levels in SKOV3-C1 than SKOV3-NV (p = .00446) (Fig. 6a). Since higher levels of MAPT together with β-tubulin correlate with paclitaxel resistance in gastric cancer , we sought to determine if HE4 affects β-tubulin levels and microtubule stability. Treatment of SKOV3-WT and OVCAR8-WT cells with 20 nM rHE4 produced a continuous increase in β-tubulin levels between 1 h and 48 h after treatment (Fig. 6b and c). Levels of α-tubulin also increased over time, similar to what was seen with β-tubulin (Fig. 6b and d). Collectively, these data suggest that HE4 may in part promote paclitaxel resistance by affecting microtubule levels or stability.
The ways in which HE4 affects chemoresistance are likely multi-factorial and cell type-specific. In cells that already display a high degree of chemoresistance due to other mechanisms, such as OVCAR8 cells, the effect of increasing levels of HE4 may be minimal. In contrast, in cells with low levels of HE4 that are not as chemoresistant, increasing the level of HE4 may produce dramatic changes in apoptotic response to drug treatment, as we have observed in SKOV3 cells.
Human HE4 purified from seminal fluid has been described to possess cross-class protease activity ; however, that study reports seminal fluid HE4 to exist as a trimer migrating at 42 kDa under non-reducing conditions and 14 kDa under SDS-PAGE reducing conditions. It is possible that HE4 from different tissues may preferentially exist in different forms, thus possessing different functions. Indeed, in our lab, we observe HE4 migrating on SDS-PAGE under reducing conditions as a 25 kDa protein, which is in agreement with a study by Drapkin et al. showing glycosylated HE4 migrating at 25 kDa in CaOV3 and OVCAR5 cells . This diversity in size may result in different enzymatic activities of HE4. If HE4 does modulate protease activity, it logically will affect a wide variety of cellular functions, since proteases are essential for many biological processes including growth factor signaling. For example, hepatocyte growth factor (HGF) , transforming growth factor beta (TGFβ) , and certain members of the platelet-derived growth factor (PDGF) family  are activated by proteases. Our data would suggest that anti-proteases may also serve a function in activating growth factor cascades in some cases.
In our current study, we have observed a variety of differences between SKOV3-NV and HE4-overexpressing cells in how they respond to cisplatin and paclitaxel. EGR1 is a transcription factor that is induced by a variety of stimuli or stresses, including growth factors, hormones, ionizing radiation, and chemotherapeutic drugs [16, 19, 33–37]. It has been shown to regulate differentiation, proliferation, and apoptosis in cell type-specific manners by promoting expression of several genes, including TP53 (p53), BCL2, PTEN, IGF2, PDGF, VEGF, TGFB1, and TNF . In our study, at 24 h after cisplatin treatment, EGR1 is upregulated in SKOV3-NV cells, but not in SKOV3-C1 or SKOV3-C7 cells. EGR1 is a transcriptional regulator of growth differentiation factor 15 (GDF15) , which was also upregulated in SKOV3-NV by cisplatin but not in SKOV3-C1 cells. While GDF15 has been linked to platinum resistance in pancreatic cancer  and ovarian cancer , it has also been shown to be a common platinum-responsive gene [41, 42], and was identified as a potential serum marker for cisplatin-response of ovarian cancer cells . Thus, the fact that it is not upregulated by cisplatin in SKOV3-C1 cells is also indicative of their dampened cisplatin resistance. Another gene, DNA-damage-inducible transcript 3 (DDIT3), was also cisplatin-induced in SKOV3-NV cells, but not SKOV3-C1 cells. Suppression of DDIT3 mRNA upregulation has been shown to be involved in chemoresistance of malignant pleural mesothelioma cells , further suggesting that multiple mechanisms may play a role in HE4-mediated chemoresistance. Lastly, tumor necrosis factor (TNF), whose gene is also EGR1-regulated , activates MAPKs and induces apoptosis ; thus, its lack of cisplatin-mediated upregulation in SKOV3-C1 cells could also contribute to suppression of pro-apoptotic signaling and cisplatin response in these cells.
EGR1 gene expression is known to be regulated by activated MAPKs, including phospho-ERK [19, 21] and phospho-p38 . Although we observe comparable increases in phospho-ERK levels in SKOV3-NV and SKOV3-C1 cells treated with 25 μM cisplatin, it is possible that HE4 affects the activity of phospho-ERK, leading to suppression of EGR1. Indeed, our results showing subtle suppression of ERK activation in HE4-overexpressing clones treated with high dose cisplatin (80 μM), as well as an effect of rHE4 on ERK activation in SKOV3-WT and OVCAR8-WT cells, support this hypothesis. HE4-mediated suppression of p38 appears to be more straightforward. We did not observe any effect of rHE4 on phospho-p38 levels (data not shown), but we did see more robust activation of p38 in SKOV3-NV cells than in SKOV3-C1 or SKOV3-C7 cells in response to two different doses of cisplatin (25 μM and 80 μM), confirming that some elements of MAPK signaling are deregulated in HE4-overexpressing cells. This suppression of p38 activation could play a role in the suppression of cisplatin-induced upregulation of EGR1.
Another significant effect that we report here is the increase in α-tubulin and β-tubulin levels in SKOV3-WT and OVCAR8-WT cells treated with rHE4. Interestingly, tubulins have been reported to be the target of the serine protease HtrA1 ; therefore, if HE4 inhibits serine protease activity, tubulins may accumulate. We postulate that the increase in tubulin levels we observe is not due to a transcriptional effect, since we did not detect an increase in any tubulin gene in OVCAR8-WT cells treated with 20 nM rHE4 for 6 h (data not shown). However, as we show here, we do see an increase in gene expression levels of MAPT in SKOV3-C1 cells compared to SKOV3-NV, which together with a putative stabilization of tubulin protein could influence paclitaxel resistance. Several lines of evidence connect β-tubulin and MAPT to taxane resistance. In addition to the correlation between MAPT and β-tubulin III levels and paclitaxel resistance in gastric cancer , downregulation of MAPT was also shown to improve taxane response in breast cancer cell lines  and in ovarian cancer three-dimensional collagen I matrix culture . Clinically, expression of the tau protein is associated with worse survival of taxane-treated breast cancer patients . Since tau proteins are responsible for stabilizing microtubules , higher levels of MAPT could affect the polymerization of microtubules by paclitaxel.
In addition to differences in how HE4-overexpressing cells respond to cisplatin, intrinsic differences between SKOV3-NV and SKOV3-C1 cells could also contribute to resistance, or could indicate other biological functions of HE4. For example, AKT3, which is more highly expressed in SKOV3-C1 cells, has been shown to promote cisplatin resistance in SKOV3 and OVCAR3 cells . Another gene of interest that is upregulated in SKOV3-C1 cells is SEPT3. The septin family of GTP-binding proteins polymerize to form cytoskeletal filaments , further implicating HE4’s putative involvement in cytoskeleton organization. Several genes that appear upregulated in HE4-overexpressing cells are in agreement with the pro-proliferative role described for HE4 [7, 11, 50], including AKT3, Ras-related GTP binding D (RRAGD), and glypican 4 (GPC4).
Several other future directions remain to clarify how HE4 promotes collateral resistance to platinum and taxane therapies. Further clarification of precisely how HE4 affects cell signaling, including MAPK signaling, in diverse cell lines is necessary. Confirmation of HE4’s anti-protease function in ovarian cancer cells would be useful in this regard. Moreover, additional information is needed on how HE4 affects tubulin organization and dynamics. Lastly, although we do not have any preliminary data to suggest that there are differences in drug uptake or clearance between SKOV3-NV and SKOV3-C1 cells, it would be necessary to measure intracellular drug levels at various time points post-treatment before ruling this out as another contributing mechanism to chemoresistance. Future studies should also address whether HE4 promotes resistance to other commonly used ovarian cancer treatments such as doxorubicin.
In summary, we have demonstrated that HE4 promotes collateral resistance to cisplatin and paclitaxel in SKOV3 and OVCAR8 ovarian cancer cells. Importantly, downregulating HE4 gene transcription using Double Nickase CRISPR/Cas technology results in reduced secretion of HE4 in SKOV3-C1 cells, and partially reverses chemoresistance. In this study, we show that there are likely multiple factors that contribute to HE4-mediated chemoresistance, although two emerging factors that we present here for the first time are deregulation of MAPK signaling and altered tubulin dynamics. As we gain a better understanding of how HE4 contributes to resistance to various chemotherapies, monitoring HE4 levels before, during, and after chemotherapy cycles may help predict responses and dictate treatment decisions. Furthermore, small molecules or antibodies targeting HE4 may enhance the efficacy of first- or second-line therapeutics and reduce the development of resistance.
Availability of datasets
The microarray dataset supporting the conclusions of this article is included within its additional file.
- C1, C5, C7:
clone 1, clone 5, clone 7
clusters of regularly interspaced short palindromic repeats
epithelial ovarian cancer
epidermal growth factor receptor
extracellular signal-regulated kinase
high grade serous ovarian cancer
mitogen activated protein kinase
poly ADP ribose polymerase
pegylated liposomal doxorubicin
quantitative reverse transcription polymerase chain reaction
recombinant human epidermal growth factor
recombinant human epididymis protein 4
risk of malignancy index
risk of ovarian malignancy algorithm
whey acidic protein
Markman M, Bookman MA. Second-line treatment of ovarian cancer. Oncologist. 2000;5:26–35.
Foley OW, Rauh-Hain JA, del Carmen MG. Recurrent epithelial ovarian cancer: an update on treatment. Oncology (Williston Park). 2013;27:288–94. 298.
Bingle L, Singleton V, Bingle CD. The putative ovarian tumour marker gene HE4 (WFDC2), is expressed in normal tissues and undergoes complex alternative splicing to yield multiple protein isoforms. Oncogene. 2002;21:2768–73.
Chhikara N, Saraswat M, Tomar A, Dey S, Singh S, Yadav S. Human epididymis protein-4 (HE-4): A novel cross-class protease inhibitor. PLoS One. 2012;7:e47672.
Heliström I, Raycraft J, Hayden-Ledbetter M, Ledbetter JA, Schummer M, McIntosh M, Drescher C, Urban N, Hellström KE. The HE4 (WFDC2) protein is a biomarker for ovarian carcinoma. Cancer Res. 2003;63:3695–700.
Moore RG, McMeekin DS, Brown AK, DiSilvestro P, Miller MC, Allard WJ, Gajewski W, Kurman R, Bast RC, Skates SJ. A novel multiple marker bioassay utilizing HE4 and CA125 for the prediction of ovarian cancer in patients with a pelvic mass. Gynecol Oncol. 2009;112:40–6.
Moore RG, Hill EK, Horan T, Yano N, Kim K, MacLaughlan S, Lambert-Messerlian G, Tseng YD, Padbury JF, Miller MC, Lange TS, Singh RK. HE4 (WFDC2) gene overexpression promotes ovarian tumor growth. Sci Rep. 2014;4:3574.
Angioli R, Capriglione S, Aloisi A, Guzzo F, Luvero D, Miranda A, Damiani P, Montera R, Terranova C, Plotti F. Can HE4 predict platinum response during first-line chemotherapy in ovarian cancer? Tumour Biol. 2014;35:7009–15.
Chudecka-Głaz AM, Cymbaluk-Płoska AA, Menkiszak JL, Sompolska-Rzechuła AM, Tołoczko-Grabarek AI, Rzepka-Górska IA. Serum HE4, CA125, YKL-40, bcl-2, cathepsin-L and prediction optimal debulking surgery, response to chemotherapy in ovarian cancer. J Ovarian Res. 2014;7:62.
Vallius T, Hynninen J, Auranen A, Carpén O, Matomäki J, Oksa S, Virtanen J, Grénman S. Serum HE4 and CA125 as predictors of response and outcome during neoadjuvant chemotherapy of advanced high-grade serous ovarian cancer. Tumour Biol. 2014;35:12389–95.
Wang H, Zhu L, Gao J, Hu Z, Lin B. Promotive role of recombinant HE4 protein in proliferation and carboplatin resistance in ovarian cancer cells. Oncol Rep. 2015;33:403–12.
Huang DW, Lempicki RA, Sherman BT. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc. 2009;4:44–57.
Huang DW, Sherman BT, Zheng X, Yang J, Imamichi T, Stephens R, Lempicki RA. Extracting biological meaning from large gene lists with DAVID. Curr Protoc Bioinforma. 2009;(13):1–13.
Dong Q, Zhang J, Hendricks DT, Zhao X. GROβ and its downstream effector EGR1 regulate cisplatin-induced apoptosis in WHCO1 cells. Oncol Rep. 2011;25:1031–7.
He J, Yu J-J, Xu Q, Wang L, Zheng JZ, Liu L-Z, Jiang B-H. Downregulation of ATG14 by EGR1-MIR152 sensitizes ovarian cancer cells to cisplatin-induced apoptosis by inhibiting cyto-protective autophagy. Autophagy. 2015;11(May):373–84.
Thiriet N, Zwiller J, Ali S. Induction of the immediate early genes egr-1 and c-fos by methamphetamine in mouse brain. Brain Res. 2001;919:31–40.
Mercier G, Turque N, Schumacher M. Early activation of transcription factor expression in Schwann cells by progesterone. Brain Res Mol Brain Res. 2001;97:137–48.
Manente AG, Pinton G, Tavian D, Lopez-Rodas G, Brunelli E, Moro L. Coordinated sumoylation and ubiquitination modulate EGF induced EGR1 expression and stability. PLoS One. 2011;6:e25676.
Gregg J, Fraizer G. Transcriptional Regulation of EGR1 by EGF and the ERK Signaling Pathway in Prostate Cancer Cells. Genes Cancer. 2011;2:900–9.
Lim C, Jain N, Cao X. Stress-induced immediate-early gene, egr-1, involves activation of p38/JNK1. Oncogene. 1998;16:2915–26.
Shi Q, Sutariya V, Bishayee A, Bhatia D. Sequential activation of Elk-1/Egr-1/GADD45α by arsenic. Oncotarget. 2014;5:3862–70.
Gurler H, Yu Y, Choi J, Kajdacsy-Balla A, Barbolina M. Three-dimensional collagen type I matrix up-regulates nuclear isoforms of the microtubule associated protein tau implicated in resistance to paclitaxel therapy in ovarian carcinoma. Int J Mol Sci. 2015;16:3419–33.
Yu J, Gao J, Lu Z, Gong J, Li Y, Dong B, Li Z, Zhang X, Shen L. Combination of microtubule associated protein-tau and β-tubulin III predicts chemosensitivity of paclitaxel in patients with advanced gastric cancer. Eur J Cancer. 2014;50:2328–35.
Ikeda H, Taira N, Hara F, Fujita T, Yamamoto H, Soh J, Toyooka S, Nogami T, Shien T, Doihara H, Miyoshi S. The estrogen receptor influences microtubule-associated protein tau (MAPT) expression and the selective estrogen receptor inhibitor fulvestrant downregulates MAPT and increases the sensitivity to taxane in breast cancer cells. Breast Cancer Res. 2010;12:R43.
Wang K, Deng Q-T, Liao N, Zhang G-C, Liu Y-H, Xu F-P, Zu J, Li X-R, Wu Y-L. Tau expression correlated with breast cancer sensitivity to taxanes-based neoadjuvant chemotherapy. Tumour Biol. 2013;34:33–8.
Wu H, Huang M, Lu M, Zhu W, Shu Y, Cao P, Liu P. Regulation of microtubule-associated protein tau (MAPT) by miR-34c-5p determines the chemosensitivity of gastric cancer to paclitaxel. Cancer Chemother Pharmacol. 2013;71:1159–71.
Rouzier R, Rajan R, Wagner P, Hess KR, Gold DL, Stec J, Ayers M, Ross JS, Zhang P, Buchholz TA, Kuerer H, Green M, Arun B, Hortobagyi GN, Symmans WF, Pusztai L. Microtubule-associated protein tau: a marker of paclitaxel sensitivity in breast cancer. Proc Natl Acad Sci U S A. 2005;102:8315–20.
Im S, Yoo C, Jung J, Jeon Y, Suh Y, Lee Y, Choi H. Microtubule-Associated Protein Tau, α-Tubulin and βIII-Tubulin Expression in Breast Cancer. Korean J Pathol. 2013;47:534–40.
Drapkin R, von Horsten HH, Lin Y, Mok SC, Crum CP, Welch WR, Hecht JL. Human epididymis protein 4 (HE4) is a secreted glycoprotein that is overexpressed by serous and endometrioid ovarian carcinomas. Cancer Res. 2005;65:2162–9.
Miyazawa K, Shimomura T, Naka D, Kitamura N. Proteolytic activation of hepatocyte growth factor in response to tissue injury. J Biol Chem. 1994;269:8966–70.
Jenkins G. The role of proteases in transforming growth factor-beta activation. Int J Biochem Cell Biol. 2008;40:1068–78.
LaRochelle WJ, Jeffers M, McDonald WF, Chillakuru RA, Giese NA, Lokker NA, Sullivan C, Boldog FL, Yang M, Vernet C, Burgess CE, Fernandes E, Deegler LL, Rittman B, Shimkets J, Shimkets RA, Rothberg JM, Lichenstein HS. PDGF-D, a new protease-activated growth factor. Nat Cell Biol. 2001;3:517–21.
Kim H-R, Kim YS, Yoon JA, Lyu SW, Shin H, Lim HJ, Hong S-H, Lee DR, Song H. Egr1 is rapidly and transiently induced by estrogen and bisphenol A via activation of nuclear estrogen receptor-dependent ERK1/2 pathway in the uterus. Reprod Toxicol. 2014;50:60–7.
Ko H, Kim J, Kim S, Shim S, Ha C, Chang H. Induction of apoptosis by genipin inhibits cell proliferation in AGS human gastric cancer cells viaEgr1/p21 signaling pathway. Bioorg Med Chem Lett. 2015;25:4191–6.
Einbond LS, Wu H-A, Su T, Chang T, Panjikaran M, Wang X, Goldsberry S. Digitoxin activates EGR1 and synergizes with paclitaxel on human breast cancer cells. J Carcinog. 2010;9:10.
Datta R, Rubin E, Sukhatme V, Qureshi S, Hallahan D, Weichselbaum RR, Kufe DW. Ionizing radiation activates transcription of the EGR1 gene via CArG elements. Proc Natl Acad Sci U S A. 1992;89:10149–53.
Arora S, Wang Y, Jia Z, Vardar-Sengul S, Munawar A, Doctor KS, Birrer M, McClelland M, Adamson E, Mercola D. Egr1 regulates the coordinated expression of numerous EGF receptor target genes as identified by ChIP-on-chip. Genome Biol. 2008;9:R166.
Baek SJ, Kim J-S, Moore SM, Lee S-H, Martinez J, Eling TE. Cyclooxygenase inhibitors induce the expression of the tumor suppressor gene EGR-1, which results in the up-regulation of NAG-1, an antitumorigenic protein. Mol Pharmacol. 2005;67:356–64.
Ji H, Lu H-W, Li Y-M, Lu L, Wang J-L, Zhang Y-F, Shang H. Twist promotes invasion and cisplatin resistance in pancreatic cancer cells through growth differentiation factor 15. Mol Med Rep. 2015;12(3):3841-8.
Meier JC, Haendler B, Seidel H, Groth P, Adams R, Ziegelbauer K, Kreft B, Beckmann G, Sommer A, Kopitz C. Knockdown of platinum-induced growth differentiation factor 15 abrogates p27-mediated tumor growth delay in the chemoresistant ovarian cancer model A2780cis. Cancer Med. 2015;4:253–67.
Altena R, Fehrmann RS, Boer H, de Vries EG, Meijer C, Gietema JA. Growth Differentiation Factor 15 (GDF-15) Plasma Levels Increase during Bleomycin- and Cisplatin-Based Treatment of Testicular Cancer Patients and Relate to Endothelial Damage. PLoS One. 2015;10:e0115372.
Konstantinopoulos PA, Fountzilas E, Pillay K, Zerbini L, Libermann TA, Cannistra SA, Spentzos D. Carboplatin-induced gene expression changes in vitro are prognostic of survival in epithelial ovarian cancer. BMC Med Genomics. 2008;1:59.
Izaguirre DI, Kwan SY, Zhifei Z, Tsang-Lee YT, Wong K-K. Abstract 3474: GDF15 as a serum marker of cisplatin response in ovarian cancer cells, AACR 104th Annu Meet Washingt DC. 2013.
Canino C, Luo Y, Marcato P, Blandino G, Pass HI, Cioce M. A STAT3-NFkB/DDIT3/CEBPβ axis modulates ALDH1A3 expression in chemoresistant cell subpopulations. Oncotarget. 2015;6:12637–53.
Wajant H, Pfizenmaier K, Scheurich P. Tumor necrosis factor signaling. Cell Death Differ. 2003;10:45–65.
Chien J, He X, Shridhar V. Identification of tubulins as substrates of serine protease HtrA1 by mixture-based oriented peptide library screening. J Cell Biochem. 2009;107:253–63.
Sabbagh JJ, Dickey CA. The Metamorphic Nature of the Tau Protein: Dynamic Flexibility Comes at a Cost. Front Neurosci. 2016;10:3.
Wu H, Xiao Z, Zhang H, Wang K, Liu W, Hao Q. MiR-489 modulates cisplatin resistance in human ovarian cancer cells by targeting Akt3. Anticancer Drugs. 2014;25:799–809.
Fung KYY, Dai L, Trimble WS. Cell and Molecular Biology of Septins. Int Rev Cell Mol Biol. 2014;310:289–339.
Zhu YF, Gao GL, Tang SB, Zhang ZD, Huang QS. Effect of WFDC 2 silencing on the proliferation, motility and invasion of human serous ovarian cancer cells in vitro. Asian Pac J Trop Med. 2013;6:265–72.
Research reported in this publication was supported by Alpert Medical School at Brown University Deans’s Emerging Areas of New Science (DEANS) Excellence Award under project number GR40003, the Kilguss Research Core of Women & Infants Hospital of Rhode Island and an Institutional Development Award (IDeA) from the National Institute of General Medical Sciences of the National Institutes of Health under grant number P30GM114750.
The authors declare that they have no competing interests.
JRR, RGM, RKS, CS and KK designed experiments. JRR executed all experiments with assistance from NR. NY developed null vector and HE4-overexpressing stable clones. CS performed the microarrays. JRR prepared this manuscript in its entirety. All authors reviewed, edited, and approved this manuscript.
HE4 overexpression enhances resistance to cisplatin and paclitaxel in OVCAR8 cells. OVCAR8-null vector (NV) and OVCAR8-HE4 clone 5 (C5) cells were treated with 0-500 μM cisplatin for 24 h (A) or 0-5 nM paclitaxel for 48 h (B), at which time the cells were subjected to MTS assay to measure viability. Error bars represent standard deviation of technical replicates. (C) OVCAR8-NV and OVCAR8-C5 cells were treated with vehicle (DMSO) or 100 μM cisplatin, and protein was collected at 24 h after treatment. Western blot was performed to detect levels of PARP and cleaved PARP. (D) Densitometry analysis of PARP and cleaved PARP normalized to β-tubulin levels, from western blot in (C). (PPTX 90 kb)
All genes differentially regulated between SKOV3-NV and SKOV3-C1 (vehicle and cisplatin treated) 1.5-fold in either direction (p < 0.05). (XLSX 209 kb)
Top 10 DAVID annotation clusters of genes differentially expressed between SKOV3-NV and SKOV3-C1. Analysis of all genes with fold-change ≥1.5 (p < .05) in either direction. (XLSX 10 kb)
Reduced transcriptional regulation by cisplatin in SKOV3-C1 cells. Scatterplots of all transcripts upregulated (green) or downregulated (red) by cisplatin in SKOV3-NV (A) and SKOV3-C1 (B) were included. Gray area represents filtered genes (fold-change <1.5 in either direction, p > .05). (PPTX 215 kb)
Overexpression of HE4 suppresses cisplatin-mediated activation of p38 and ERK. (A) SKOV3-NV, SKOV3-C1, and SKOV3-C7 cells were treated with vehicle (DMSO) or 80 μM cisplatin for the indicated times. Western blot was performed to detect levels of phospho-p38 and total p38. (B) Densitometry analysis of p-p38/p38 ratio from (A). (C) Densitometry analysis of phospho-ERK/ERK ratio from (A). (PPTX 443 kb)