Medroxyprogesterone acetate causes the alterations of endoplasmic reticulum related mRNAs and lncRNAs in endometrial cancer cells
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Progestin is effective to promote endometrial cancer (EC) cells apoptosis, however, continuous progestin administration causes low level of progestin receptor B (PRB), further resulting in progestin resistance. Here, we performed microarray analysis on Ishikawa cells (PRB+) treated with medroxyprogesterone acetate (MPA) to explore the molecular mechanism underlying the inhibitory influence of MPA on PRB+ EC cells.
Microarray analysis was performed by using Ishikawa cells (PRB+) treated with MPA. Differentially expressed mRNA and long noncoding RNAs (lncRNAs) were identified. Furthermore, the functions of these mRNAs and lncRNAs were predicted by functional enrichment analysis. QRT-PCR was further performed to verify the microarray data.
A total of 358 differentially expressed genes and 292 lncRNAs were identified in Ishikawa cells (PRB+) treated with MPA. QRT-PCR verified these data. Functional enrichment analysis identified endoplasmic reticulum (ER) stress as the key pathway involved in the inhibitory effect of MPA on EC cells. And the ER stress apoptotic molecule CHOP and ER stress related molecule HERPUD1 were both highly expressed in Ishikawa cells (PRB+) treated with MPA. Co-expression analysis showed lnc-CETP-3 was highly correlated with CHOP and HERPUD1, suggesting it might participate in ER stress pathway-related EC cell apoptosis caused by MPA. In addition, compared with untreated cells, lnc-CETP-3, CHOP and HERPUD1 were significantly up-regulated in Ishikawa cells (PRB+) treated with MPA, whereas they have no statistical significance in KLE cells (PRB-).
MPA may activate ER stress by progesterone-PRB pathway to up-regulate CHOP expression, which may be one of the molecular mechanisms underlying the inhibitory effect of MPA on EC cells with PRB+. Lnc-CETP-3 might be involved in this process. These findings may provide therapeutic targets for EC patients with PRB-, and resistance-related targets to increase the sensitivity of MPA on EC cells.
KeywordsEndometrial cancer Medroxyprogesterone acetate Endoplasmic reticulum stress CHOP Lnc-CETP-3
Activating AMP-activated protein kinase
American Type Culture Collection
Activating transcription factor 6
CCAAT/enhancer-binding protein homologous protein
Dulbecco’s modified Eagle’s medium
Dopamine receptor D2
Epidermal growth factor receptor
Fetal bovine serum
Homocysteine-inducible, endoplasmic reticulum stress-inducible, ubiquitin-like domain member 1
Insulin-like growth factor II
Inositol-requiring enzyme 1
Kyoto Encyclopedia of Genes and Genomes
Long noncoding RNAs
Mitogen-activated protein kinase
PKR-like ER kinase
Progestin receptor B
Endometrial carcinoma (EC) is the most common malignant tumor of the female reproductive tract resulting in 70,000 deaths worldwide annually . Medroxyprogesterone acetate (MPA), a steroidal progestin, has been used as a conservative treatment for young patients with clinical stage I, grade I EC for a long time, which is desirable in patients hoping to preserve fertility . The overall response rate of progestin treatment for EC ranges from 15 to 40% . When treated with MAP, 10 mg daily for 12–14 days each month, 80–90% patients have regressed hyperplasia without atypia to normal endometrium . However, most patients with EC develop progestin-resistance though they initially respond to progestin treatment, which further causes tumor progression . A study has reported that 62% of patients with EC have an initial response to progestin, and 23% of initial responders later have developed recurrent disease . In addition, > 30% of young patients have no response to progestin due to de novo or acquired progestin resistance during treatment . However, the mechanism underlying progestin resistance remains largely unrevealed.
At present, many studies have reported some possible factors associated with progestin resistance. Low expression level of progestin receptor (PR) caused by continuous progestin administration is regarded as one of the reasons since it further decreases the sensitivity of cancer cells to progestin . The other molecules including up-regulation of growth factors or their receptors contribute to progestin resistance. Increased level of epidermal growth factor receptor (EGFR) reduces Ishikawa EC cells sensitivity to progestin and PR expression, and abnormally activated the mitogen-activated protein kinase (MAPK) signaling pathway . Overexpression of insulin-like growth factor II (IGF-II) inhibited PR expression partially mediating through activating AMP-activated protein kinase (AMPK) and inhibiting the over activated mTOR pathway . In addition, activation of the PI3K/Akt pathway by progestin without PR mediation also causes progestin resistance to EC cells, and inhibiting this pathway is considered as an effective method to reverse resistance . These reports suggest that the association with PR does not fully explain the mechanism of progestin resistance. Our previous studies have found RANK-RANKL (the targeting of receptor activator of nuclear factor-κB ligand) system promotes EC progression via MAPK pathway  and epithelial-mesenchymal transition (EMT) , and induces EC metastasis mediated by AKT/β-catenin/Snail pathway both in vitro and in vivo . We further find that a combination of thioridazine (THIO) and MAP significantly enhances the expression levels of MPA-mediated progesterone receptor B (PRB) and dopamine receptor D2 (DRD2), and decreases the ratio of p-AKT/AKT in PI3K/AKT signal pathway, which further inhibits EC cells proliferation and promotes cell apoptosis .
Long noncoding RNAs (lncRNAs) encoded by a vast less explores region of the human genome, have been reported to be biomarkers and therapeutic targets for cancer, since they play a critical in promoting and maintaining tumor initiation and progression . LncRNAs interact with proteins, RNA, and lipids, suggesting that they are essential mediators of cancer signaling pathways. In addition, the dysregulation of lncRNAs is associated with the stage and prognosis of many tumor types, including EC, as well as involved in resistance against chemotherapy and targeted therapy . Previous studies have identified several lncRNAs correlated with EC progression. LncRNA-GAS5 promotes EC cell apoptosis by regulating the expression of miR-103 and PTEN . High expression level of lncRNA BANCR in type 1 EC tissue promotes cell proliferation, migration and invasion by activating ERK/MAPK signaling pathway . LncRNA HOTAIR regulates NPM1 via interacting with miR-646, and further mediates the estrogem-induced metastasis of EC cells . High levels of lncRNA MALAT1 have been reported in EC, which is associated with the aberrant activation of the wnt/beta-catenin pathway leading to the interaction of wnt-effector transcription factor TCF4 and MALAT1 promoter region . Furthermore, lncRNA LINC00672 has been demonstrated to increase the sensitivity of EC xenograft mice to paclitaxel . Though various lncRNAs show a relationship to EC progression, to our knowledge, the association between lncRNAs and progestin resistance in EC cells has not been evaluated.
Here, to explore the molecular mechanism underlying the inhibitory influence of MPA on PRB+ EC cells, we performed microarray to analyze the mRNA and lncRNA expression profiling between Ishikawa cells (stably expressing PRB) with MPA treatment and untreated cells. And then, differentially expressed genes and lncRNAs were identified. To predict the functions of these genes and lncRNAs in EC, we further performed functional enrichment analysis. The results showed that endoplasmic reticulum stress (ER stress) might be involved in the influence of MAP on EC progression. We further used CHOP (ER stress apoptotic molecule) and HERPUD1 (ER stress related molecule) to performed co-expression analysis, and found lnc-CETP-3 was significantly increased, and closely correlated with CHOP and HERPUD1 expression. The functional enrichment analysis based on the co-expression mRNAs of lnc-CETP-3 showed that lnc-CETP-3 was involved in cell apoptosis, cell cycle, ER stress, and cancer pathway. To validate the reliability of microarray data, we further evaluated the expression levels of selected lncRNAs by qRT-PCR. CHOP, HERPUD1 and lnc-CETP-3 were significantly increased in PRB+ EC cells, whereas they have no statistical significance in PRB- EC cells.
Ishikawa cell line (ATCC® 13,347™) and KLE cell line (ATCC® CRL-1622™) were purchased from American Type Culture Collection (ATCC). Cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM) F12 medium (Hyclone # SH3026101) with 10% fetal bovine serum (FBS) (Hyclone # SH30071) and 1% Penicillin/Streptomycin (Gibco # 15140) at 37 °C in a humidified atmosphere of 5% CO2.
RNA isolation and qualification
In consistent with previous studies [2, 8], 10 umol/L MPA (selleck, USA) were added into treated groups, and DMSO were added into control groups. The final concentration of DMSO did not exceed 0.1%. After 48 h, all cells were washed and collected.
Total RNA was extracted using TRIzol reagent (Invitrogen life, USA). In brief, cultured cells were washed with PBS and lysed with TRIzol reagent. After homogenization, added chloroform to TRIzol reagent. Following centrifugation, the mixture separated into two layers and the aqueous phase with RNA was transferred to a new tube. RNA was precipitated by mixing with ethanol and centrifugation. After washing with ethanol the RNA was dissolved in DEPC-treated water. NanoDrop ultraviolet spectrophotometer (Thermo Fisher Scientific, Waltham, MA, USA) was used to evaluate the purity of RNA with a 260/280 ration of ~ 2.0 and a 260/230 ratio between 2.0–2.2. An average of 10 μg RNA was purified using RNeasy Mini Kit (Qiagen, Hilden, Germany). The isolated RNA was stored at − 80 °C until assayed.
The purified RNA was used to construct cDNA libraries by using TruSeq RNA Sample Preparation Kit (Illumina, San Diego, CA, USA) according to manufacturer’s instruction. Following first and second cDNA strands synthesis, samples were then amplified and transcribed into fluorescent cRNA. The labeled cRNAs were further purified, and reverse transcribed to 2nd-cycle cDNA. After purification and fragmentation, 2nd-cycle cDNA was then labeled. The hybridization solution mixed with labeled cDNA, hybridization buffer and other buffers was divided into the gasket slide and arranged on the lncRNA expression microarray slide. The slides were incubated in Hybridization Oven (Affymetrix) at the temperature of 45 °C for 16 h. After hybridization, the arrays were washed, fixed, and last scanned by using a scanner (Affymetrix).
Differentially expressed mRNA and lncRNA analysis
To identify differentially expressed mRNAs and lncRNAs, the expression levels in EC cells treated with MPA were compared with their respective expression levels in untreated cells. Statistical significance was identified through the filtering of both P value and FDR. |Log2(Fold change)| > 1 and P < 0.05 were set as threshold.
Functional enrichment analysis
To predict the functions of the differentially expressed mRNAs or lncRNAs, Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were performed . GO terms included three parts, molecular function (MF), biological process (BP) and cellular component (CC). Hypergeometric distribution test was performed to calculate the significance of each term or pathway. P < 0.05 was set as a threshold. The Pearson correlation coefficient between each lncRNA and mRNA was evaluated. When p value was less than 0.05, and the absolute value of Pearson correlation coefficient was more than 0.7, the lncRNA and mRNA were correlated.
Co-expression network analysis
To identify the interactions between mRNAs and lncRNAs, we performed co-expression network analysis. CHOP and HERPUD1 were selected as center genes, and we screened the lncRNAs co-expressed with the two genes. LncRNA-mRNA interaction analysis was performed by popular target prediction software, and network was constructed by Cytoscape software.
Quantitative real-time PCR analysis
Total RNA was reverse transcribed to cDNA by using SuperScript™ III Reverse Transcriptase (Invitrogen, Carlsbad, CA) according to the manufacturer’s protocol. The expression levels of circRNAs were determined by ViiA 7 Real-time PCR System (Applied Biosystems, Foster City, CA). Triplicates were performed for each sample in three independent experiments. GAPDH serves as control. Primers: for lnc-CETP-3, 5′-TCAGGGTGCTGCTGTGATTA-3′ (forward), 5′-CACAGTGAGACTTACTCAAGAA-3′ (reverse); for lnc-SLC-12A3–1, 5′-CTGCCTCTTCATGATGGT-3′ (forward), 5′-CCAACTTCTTTTATTACTCCCC-3′ (reverse); for lncSAP130–1, 5′-ACAAAGTCGTTGAAATGGTAGT-3′ (forward), 5′-GTTAACAAGCAGTGGGTCTC-3′ (reverse); for LncATF3–3, 5′-CTGTCTGGACTGTGCTAAT-3′ (forward), 5′-TTGGTTCCCAAGGGACAA-3′ (reverse); for GAPDH, 5′- TCGGAGTCAACGGATTTGGT-3′ (forward), 5′- TTGCCATGGGTGGAATCATA-3′ (reverse). The relative mRNA expression was calculated using the equation: 2-∆∆Ct.
Data of qRT-PCR were presented as mean ± SEM. The comparisons between two groups were performed using Student’s t test. A value of P < 0.05 was considered to be statistically significant.
Identification of differentially expressed mRNAs and lncRNAs
The number of differentially expressed mRNA and lncRNA in Ishikawa cells treated with MPA compared with untreated cells
Differentially expressed mRNAs
Differentially expressed lncRNAs
The functional enrichment analysis based on differentially expressed genes
The biological processes related to ER stress/unfolded protein response
endoplasmic reticulum unfolded protein response
response to unfolded protein
IRE-1mediated unfolded protein response
response to endoplasmic reticulum stress
KEGG pathway analysis revealed that the differentially expressed genes were mainly enriched in protein processing in endoplasmic reticulum, protein export, cell cycle, and other tumor-related pathways (Fig. 2d).
The expression levels of genes in ER stress pathway
The expression levels of mRNAs related to ER stress
The function prediction of differentially expressed lncRNAs
Lnc-CETP-3 was screened as key lncRNA
The expression of ER stress-related genes (CHOP and HERPUD1) and lncRNA (lnc-CETP-3) in Ishikawa cells (PRB+) and KLE cells (PRB-)
Our microarray data detected the changes of mRNA and lncRNA expression profiling of Ishikawa cells stably expressing progesterone receptor B (PRB) (PRB+). To confirm that MPA induced the above expression changes by PRB, we evaluated the expression of ER stress-related genes and lncRNA, including CHOP, HERPUD1 and lnc-CETP-3, in KLE cells poorly expressing PRB (PRB-). After treated with MPA, the mRNA levels of CHOP, HERPUD1 and lnc-CETP-3 were all significantly increased in Ishikawa cells. However, their expression levels have no statistical significance in KLE cells treated with MPA compared with untreated KLE cells (Fig. 6b-d). These findings suggested that MPA might induced the mRNA and lncRNA expression changes by PRB.
Patients with positive-PR EC are correlated strongly with successful endocrine treatment and survival, whereas negative-PR EC are linked to progestin resistance and EC progression, since PR expression, especially PRB, is essential to progestin action . Previous study has reported that PRB plays a key role in the inhibitory effects of progestin on cell growth and invasiveness, and a low PRB expression level generally represents a poor prognosis for EC patients with MPA resistance . This study aimed at exploring the molecular mechanism underlying the influence of MPA on EC cells with PRB+, which may provide therapeutic targets for EC patients with PRB-, and resistance-related targets to increase the sensitivity of MPA on EC cells.
In this study, we sought to identify the differentially expressed genes and lncRNAs in PRB-positive Ishikawa cells treated with MPA. Co-expression analysis as well as GO terms and KEGG pathways analyses were all revealed that MPA activated the endoplasmic reticulum unfolded protein response in Ishikawa cells. Endoplasmic reticulum (ER), an extensive intracellular organelle, provides a site for protein modification and folding as well as intracellular calcium (Ca2+) store . ER stress is characterized by accumulation of abnormal proteins, such as unfolding or misfolding proteins in the ER and overloading of Ca2+ into the mitochondria, which result from DNA damage, hypoxia, oxidative stress, and other types of physiological and pathological stimuli . At the beginning of ER stress, cells activate the unfolded protein response (UPR) which is mainly regulated by three ER-located sensors, including PKR-like ER kinase (PERK), inositol-requiring enzyme 1 (IRE1) and activating transcription factor 6 (ATF6). Theses sensors initiate translational attenuation to inhibit further accumulation of misfolded proteins and to increase folding machinery, and facilitate ER-associated degradation to eliminate misfolded proteins in the ER . If UPR is insufficient to alleviate the stress, it then leads to cell death . Previous study has demonstrated that ER stress reduces chemotherapy resistance by down-regulating the PI3K/Akt/mTOR signaling pathway in mutant p53 lung cancer cells . In this study, we found that ER stress-related genes, including CHOP, HERPUD1, ATF6 and GADD34, were highly expressed induced by MPA in EC cells. Among them, CHOP was significantly increased with the fold change of 35.37. CHOP, the best-characterized factor in the transition from ER stress to apoptosis, is expressed at low levels under physiological conditions, whereas is dramatically increased under severe and prolonged ER stress [23, 27]. It has been reported that ER stress by realgar quantum dots induces increased expression of CHOP, and further leads to EC cell apoptosis and necrosis . Additionally, previous study has demonstrated that progesterone-induced ER stress may enhance EC apoptosis through overexpression of CHOP . Our microarray data showed that HERPUD1 is also significantly increased with the fold change of 11.94. HERPUD1 (homocysteine-inducible, endoplasmic reticulum stress-inducible, ubiquitin-like domain member 1), an ER-resident membrane protein, facilitate ER-associated degradation, and its expression is strongly up-regulated by the unfolded protein response and cellular stress [29, 30]. We further constructed a co-expressed network based on the differentially expressed lncRNAs interacted with CHOP and HERPUD1. A total of 277 lncRNAs were interacted with both of the genes, among which lnc-CETP-3 was highly expressed with the fold change of 15.26, and closely correlated with the expression of CHOP and HERPUD1. Functional prediction analysis showed that lnc-CETP-3 was associated with endoplasmic reticulum unfolded protein response, apoptosis, cell cycle, and tumor-related pathways. These findings suggest that ER stress and lnc-CETP-3 are likely to be involved in the influence of MPA on Ishikawa cells (PRB+).
To further detect the influence of PRB on the expression of lnc-CETP-3, CHOP and HERPUD1 in EC cells treated with MPA, we selected Ishikawa cells (PRB+) and KLE cells (PRB-). QRT-PCR results showed that lnc-CETP-3, CHOP and HERPUD1 were all significantly up-regulated in Ishikawa cells treated with MPA compared with untreated Ishikawa cells, whereas their expression levels have no statistical significance in KLE cells treated with MPA compared with untreated KLE cells. These findings reveal that MPA activates ER stress and increased the expression of lnc-CETP-3 by PRB, and this may be one of the molecular mechanisms underlying the inhibitory effect of MPA on EC cells. In other word, ER stress and lnc-CETP-3 may be as therapeutic targets for patients with PRB- EC or even MPA resistance patients.
There are still many deficiencies in this study. We just predicted that MPA activated ER stress and increased the expression of CHOP to cause EC cells apoptosis, and lnc-CETP-3 might be involved in ER stress regulation. However, this prediction has not been further verified. Thus, we prepare to explore the roles of CHOP and lnc-CETP-3 in the influence of MPA on EC cells, and to confirm whether MPA-PRB-lnc-CETP-3/ERS-CHOP apoptotic pathways exist in subsequent studies. In addition, the association between CHOP, lnc-CETP-3 and PRB should be further verified in animal and human studies.
In this study, we concluded that MPA activated ER stress by progesterone-PRB pathway to up-regulate CHOP expression, which may be one of the molecular mechanisms underlying the inhibitory effect of MPA on EC cells with PRB+. Lnc-CETP-3 might be involved in this process. These findings may provide therapeutic targets for EC patients with PRB-, and resistance-related targets to increase the sensitivity of MPA on EC cells.
WC collected the experimental data and written the manuscript. WG performed bioinformatics analysis. PZ contributed to the design of primers. XS contributed to the statistics analysis. LW designed this study and writtern the manuscript. All authors read and approved the final manuscript.
This work was supported by the National Natural Science Foundation of China (No.81572547). The funding body has no role in the design of the study, collection, analysis, and interpretation of data, or in writing the manuscript.
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The authors declare that they have no competing interests.
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