Identification of EMP1 as a critical gene for cisplatin resistance in ovarian cancer by using integrated bioinformatics analysis

Abstract Background Cisplatin resistance is among the main reasons for the poor prognosis of ovarian cancer (OC) patients. Until now, effective biomarkers for predicting cisplatin resistance in OC and specific drugs for reversing this resistance are lacking. This study identified the critical gene a...

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Main Authors: Qingsong Zeng, Cunjian Yi, Jinzhi Lu, Xiaowen Wang, Keming Chen, Li Hong
Format: Article
Language:English
Published: Wiley 2023-04-01
Series:Cancer Medicine
Subjects:
Online Access:https://doi.org/10.1002/cam4.5637
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author Qingsong Zeng
Cunjian Yi
Jinzhi Lu
Xiaowen Wang
Keming Chen
Li Hong
author_facet Qingsong Zeng
Cunjian Yi
Jinzhi Lu
Xiaowen Wang
Keming Chen
Li Hong
author_sort Qingsong Zeng
collection DOAJ
description Abstract Background Cisplatin resistance is among the main reasons for the poor prognosis of ovarian cancer (OC) patients. Until now, effective biomarkers for predicting cisplatin resistance in OC and specific drugs for reversing this resistance are lacking. This study identified the critical gene associated with cisplatin resistance in OC and provided a potential target for overcoming this resistance. Methods Differentially expressed genes between cisplatin‐resistant and ‐sensitive OCs were identified by screening public datasets. Survival analysis was conducted to screen prognosis‐related DEGs. CIBERSORT, ESTIMATE, and immune checkpoint genes were used to assess the association between EMP1 expression and tumor microenvironment features. CTRP and GDSC databases were employed to analyze the correlation between EMP1 expression and cisplatin resistance. Furthermore, immunohistochemistry, qPCR, Western blotting, siRNA interference, and the CCK8 assay were performed to verify the role of EMP1 in cisplatin resistance in vitro. Finally, xenograft mouse models were generated to further confirm the role of EMP1 in cisplatin resistance in vivo. Results EMP1 was identified as a critical gene associated with cisplatin resistance in OC. According to bioinformatics analyses, increased EMP1 expression was linked to higher stromal/ESTIMATE scores as well as greater ICG expression levels. The in vitro experiments showed that EMP1 was highly expressed in cisplatin‐resistant OC tissues and cells, and silencing this EMP1 expression enhanced OC cell sensitivity to cisplatin. Finally, in vivo experiments confirmed that EMP1 promotes tumor growth and cisplatin resistance. Conclusions EMP1 can act as a predictive biomarker for cisplatin resistance in OC and as a potential therapeutic target.
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spelling doaj.art-1580e0dac0e64512a41af32c79d3ad3b2023-04-27T10:12:44ZengWileyCancer Medicine2045-76342023-04-011279024904010.1002/cam4.5637Identification of EMP1 as a critical gene for cisplatin resistance in ovarian cancer by using integrated bioinformatics analysisQingsong Zeng0Cunjian Yi1Jinzhi Lu2Xiaowen Wang3Keming Chen4Li Hong5Department of Obstetrics and Gynecology Renmin Hospital of Wuhan University Wuhan Hubei ChinaDepartment of Obstetrics and Gynecology Hubei Clinical Medicine Research Center for Individualized Cancer Diagnosis and Therapy, The First Affiliated Hospital of Yangtze University Jingzhou Hubei ChinaDepartment of Laboratory Medicine Hubei Clinical Medicine Research Center for Individualized Cancer Diagnosis and Therapy, The First Affiliated Hospital of Yangtze University Jingzhou Hubei ChinaDepartment of Obstetrics and Gynecology Hubei Clinical Medicine Research Center for Individualized Cancer Diagnosis and Therapy, The First Affiliated Hospital of Yangtze University Jingzhou Hubei ChinaDepartment of Obstetrics and Gynecology Hubei Clinical Medicine Research Center for Individualized Cancer Diagnosis and Therapy, The First Affiliated Hospital of Yangtze University Jingzhou Hubei ChinaDepartment of Obstetrics and Gynecology Renmin Hospital of Wuhan University Wuhan Hubei ChinaAbstract Background Cisplatin resistance is among the main reasons for the poor prognosis of ovarian cancer (OC) patients. Until now, effective biomarkers for predicting cisplatin resistance in OC and specific drugs for reversing this resistance are lacking. This study identified the critical gene associated with cisplatin resistance in OC and provided a potential target for overcoming this resistance. Methods Differentially expressed genes between cisplatin‐resistant and ‐sensitive OCs were identified by screening public datasets. Survival analysis was conducted to screen prognosis‐related DEGs. CIBERSORT, ESTIMATE, and immune checkpoint genes were used to assess the association between EMP1 expression and tumor microenvironment features. CTRP and GDSC databases were employed to analyze the correlation between EMP1 expression and cisplatin resistance. Furthermore, immunohistochemistry, qPCR, Western blotting, siRNA interference, and the CCK8 assay were performed to verify the role of EMP1 in cisplatin resistance in vitro. Finally, xenograft mouse models were generated to further confirm the role of EMP1 in cisplatin resistance in vivo. Results EMP1 was identified as a critical gene associated with cisplatin resistance in OC. According to bioinformatics analyses, increased EMP1 expression was linked to higher stromal/ESTIMATE scores as well as greater ICG expression levels. The in vitro experiments showed that EMP1 was highly expressed in cisplatin‐resistant OC tissues and cells, and silencing this EMP1 expression enhanced OC cell sensitivity to cisplatin. Finally, in vivo experiments confirmed that EMP1 promotes tumor growth and cisplatin resistance. Conclusions EMP1 can act as a predictive biomarker for cisplatin resistance in OC and as a potential therapeutic target.https://doi.org/10.1002/cam4.5637cisplatin resistancedifferential expression genesfunctional enrichment analysisovarian cancersurvival analysis
spellingShingle Qingsong Zeng
Cunjian Yi
Jinzhi Lu
Xiaowen Wang
Keming Chen
Li Hong
Identification of EMP1 as a critical gene for cisplatin resistance in ovarian cancer by using integrated bioinformatics analysis
Cancer Medicine
cisplatin resistance
differential expression genes
functional enrichment analysis
ovarian cancer
survival analysis
title Identification of EMP1 as a critical gene for cisplatin resistance in ovarian cancer by using integrated bioinformatics analysis
title_full Identification of EMP1 as a critical gene for cisplatin resistance in ovarian cancer by using integrated bioinformatics analysis
title_fullStr Identification of EMP1 as a critical gene for cisplatin resistance in ovarian cancer by using integrated bioinformatics analysis
title_full_unstemmed Identification of EMP1 as a critical gene for cisplatin resistance in ovarian cancer by using integrated bioinformatics analysis
title_short Identification of EMP1 as a critical gene for cisplatin resistance in ovarian cancer by using integrated bioinformatics analysis
title_sort identification of emp1 as a critical gene for cisplatin resistance in ovarian cancer by using integrated bioinformatics analysis
topic cisplatin resistance
differential expression genes
functional enrichment analysis
ovarian cancer
survival analysis
url https://doi.org/10.1002/cam4.5637
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