Analysis of carcinogenic signaling networks in endometrial cancer identifies RAB17 as a potential target
Endometrial cancer is one of the most common malignancies in postmenopausal women. Several potential therapeutic targets have been investigated in current research, but few have been used clinically. Therefore, further investigating the potential pathogenesis of endometrial cancer and new effective...
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Veröffentlicht in: | Journal of cellular physiology 2021-01, Vol.236 (1), p.328-339 |
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creator | Zhou, Xing Xia, Geqing Liu, Yan Xin, Xiaoyan Shi, Rui An, Lanfen Zhang, Jun Zhao, Rong Zhao, Yingchao Wang, Hongbo |
description | Endometrial cancer is one of the most common malignancies in postmenopausal women. Several potential therapeutic targets have been investigated in current research, but few have been used clinically. Therefore, further investigating the potential pathogenesis of endometrial cancer and new effective therapeutic targets for endometrial malignancies is still necessary. Our study used a The Cancer Genome Atlas dataset and two Gene Expression Omnibus datasets for weighted gene coexpression network analysis to identify important genes associated with the histological grades of endometrial cancer. In addition, we performed gene set enrichment analysis on the three datasets and found that abnormally activated signaling pathways and metabolic pathways are the main biological behaviors of endometrial cancer. Moreover, we further used different algorithms and identified the RAB17 gene as a potential study object. To further illustrate the potential role of the genes we analyzed in clinical and cellular aspects, we performed a clinical correlation analysis. Finally, we demonstrated the important roles and mechanisms of the RAB17 gene in the cell cycle, proliferation, and metastasis of endometrial cancer. Using repeated database analysis and cell‐level assays, we propose RAB17 as a potential target gene for endometrial cancer for further study.
We demonstrated the important roles and mechanisms of the RAB17 gene in the cell cycle, proliferation, and metastasis of endometrial cancer. Using repeated database analysis and cell‐level assays, we propose RAB17 as a potential target gene for endometrial cancer for further study. |
doi_str_mv | 10.1002/jcp.29845 |
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We demonstrated the important roles and mechanisms of the RAB17 gene in the cell cycle, proliferation, and metastasis of endometrial cancer. Using repeated database analysis and cell‐level assays, we propose RAB17 as a potential target gene for endometrial cancer for further study.</description><identifier>ISSN: 0021-9541</identifier><identifier>EISSN: 1097-4652</identifier><identifier>DOI: 10.1002/jcp.29845</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc</publisher><subject>Algorithms ; Cancer ; Carcinogens ; Cell cycle ; Correlation analysis ; Datasets ; Endometrial cancer ; Endometrium ; Gene expression ; Gene set enrichment analysis ; Genes ; Genomes ; Metabolic pathways ; Metastases ; metastasis ; Network analysis ; Pathogenesis ; Post-menopause ; proliferation ; RAB17 ; Signal transduction ; Signaling ; Therapeutic applications ; WGCNA</subject><ispartof>Journal of cellular physiology, 2021-01, Vol.236 (1), p.328-339</ispartof><rights>2020 Wiley Periodicals LLC</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3305-81c931df0b03edf497a82c9adc4e7127ed014f421facee826bf44b9744b1ee8d3</citedby><cites>FETCH-LOGICAL-c3305-81c931df0b03edf497a82c9adc4e7127ed014f421facee826bf44b9744b1ee8d3</cites><orcidid>0000-0002-4783-4120</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjcp.29845$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjcp.29845$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Zhou, Xing</creatorcontrib><creatorcontrib>Xia, Geqing</creatorcontrib><creatorcontrib>Liu, Yan</creatorcontrib><creatorcontrib>Xin, Xiaoyan</creatorcontrib><creatorcontrib>Shi, Rui</creatorcontrib><creatorcontrib>An, Lanfen</creatorcontrib><creatorcontrib>Zhang, Jun</creatorcontrib><creatorcontrib>Zhao, Rong</creatorcontrib><creatorcontrib>Zhao, Yingchao</creatorcontrib><creatorcontrib>Wang, Hongbo</creatorcontrib><title>Analysis of carcinogenic signaling networks in endometrial cancer identifies RAB17 as a potential target</title><title>Journal of cellular physiology</title><description>Endometrial cancer is one of the most common malignancies in postmenopausal women. Several potential therapeutic targets have been investigated in current research, but few have been used clinically. Therefore, further investigating the potential pathogenesis of endometrial cancer and new effective therapeutic targets for endometrial malignancies is still necessary. Our study used a The Cancer Genome Atlas dataset and two Gene Expression Omnibus datasets for weighted gene coexpression network analysis to identify important genes associated with the histological grades of endometrial cancer. In addition, we performed gene set enrichment analysis on the three datasets and found that abnormally activated signaling pathways and metabolic pathways are the main biological behaviors of endometrial cancer. Moreover, we further used different algorithms and identified the RAB17 gene as a potential study object. To further illustrate the potential role of the genes we analyzed in clinical and cellular aspects, we performed a clinical correlation analysis. Finally, we demonstrated the important roles and mechanisms of the RAB17 gene in the cell cycle, proliferation, and metastasis of endometrial cancer. Using repeated database analysis and cell‐level assays, we propose RAB17 as a potential target gene for endometrial cancer for further study.
We demonstrated the important roles and mechanisms of the RAB17 gene in the cell cycle, proliferation, and metastasis of endometrial cancer. Using repeated database analysis and cell‐level assays, we propose RAB17 as a potential target gene for endometrial cancer for further study.</description><subject>Algorithms</subject><subject>Cancer</subject><subject>Carcinogens</subject><subject>Cell cycle</subject><subject>Correlation analysis</subject><subject>Datasets</subject><subject>Endometrial cancer</subject><subject>Endometrium</subject><subject>Gene expression</subject><subject>Gene set enrichment analysis</subject><subject>Genes</subject><subject>Genomes</subject><subject>Metabolic pathways</subject><subject>Metastases</subject><subject>metastasis</subject><subject>Network analysis</subject><subject>Pathogenesis</subject><subject>Post-menopause</subject><subject>proliferation</subject><subject>RAB17</subject><subject>Signal transduction</subject><subject>Signaling</subject><subject>Therapeutic applications</subject><subject>WGCNA</subject><issn>0021-9541</issn><issn>1097-4652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kE1LAzEQhoMoWKsH_0HAk4dtk2z2I8da_KSgiJ5Dmp2sqdtkTbaU_nuj69XLDDPvMy_Mi9AlJTNKCJtvdD9joubFEZpQIqqMlwU7RpOk0UwUnJ6isxg3hBAh8nyCPhZOdYdoI_YGaxW0db4FZzWOtk2SdS12MOx9-IzYOgyu8VsYglVdwp2GgG0DbrDGQsSvixtaYRWxwr0fftYJG1RoYThHJ0Z1ES7--hS9392-LR-y1fP943KxynSekyKrqRY5bQxZkxwaw0WlaqaFajSHirIKGkK54YwapQFqVq4N52tRpULT3ORTdDX69sF_7SAOcuN3IX0SJeMlq4qS8CJR1yOlg48xgJF9sFsVDpIS-ROkTEHK3yATOx_Zve3g8D8on5Yv48U3HjJ12Q</recordid><startdate>202101</startdate><enddate>202101</enddate><creator>Zhou, Xing</creator><creator>Xia, Geqing</creator><creator>Liu, Yan</creator><creator>Xin, Xiaoyan</creator><creator>Shi, Rui</creator><creator>An, Lanfen</creator><creator>Zhang, Jun</creator><creator>Zhao, Rong</creator><creator>Zhao, Yingchao</creator><creator>Wang, Hongbo</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><orcidid>https://orcid.org/0000-0002-4783-4120</orcidid></search><sort><creationdate>202101</creationdate><title>Analysis of carcinogenic signaling networks in endometrial cancer identifies RAB17 as a potential target</title><author>Zhou, Xing ; Xia, Geqing ; Liu, Yan ; Xin, Xiaoyan ; Shi, Rui ; An, Lanfen ; Zhang, Jun ; Zhao, Rong ; Zhao, Yingchao ; Wang, Hongbo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3305-81c931df0b03edf497a82c9adc4e7127ed014f421facee826bf44b9744b1ee8d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Algorithms</topic><topic>Cancer</topic><topic>Carcinogens</topic><topic>Cell cycle</topic><topic>Correlation analysis</topic><topic>Datasets</topic><topic>Endometrial cancer</topic><topic>Endometrium</topic><topic>Gene expression</topic><topic>Gene set enrichment analysis</topic><topic>Genes</topic><topic>Genomes</topic><topic>Metabolic pathways</topic><topic>Metastases</topic><topic>metastasis</topic><topic>Network analysis</topic><topic>Pathogenesis</topic><topic>Post-menopause</topic><topic>proliferation</topic><topic>RAB17</topic><topic>Signal transduction</topic><topic>Signaling</topic><topic>Therapeutic applications</topic><topic>WGCNA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Xing</creatorcontrib><creatorcontrib>Xia, Geqing</creatorcontrib><creatorcontrib>Liu, Yan</creatorcontrib><creatorcontrib>Xin, Xiaoyan</creatorcontrib><creatorcontrib>Shi, Rui</creatorcontrib><creatorcontrib>An, Lanfen</creatorcontrib><creatorcontrib>Zhang, Jun</creatorcontrib><creatorcontrib>Zhao, Rong</creatorcontrib><creatorcontrib>Zhao, Yingchao</creatorcontrib><creatorcontrib>Wang, Hongbo</creatorcontrib><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Journal of cellular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Xing</au><au>Xia, Geqing</au><au>Liu, Yan</au><au>Xin, Xiaoyan</au><au>Shi, Rui</au><au>An, Lanfen</au><au>Zhang, Jun</au><au>Zhao, Rong</au><au>Zhao, Yingchao</au><au>Wang, Hongbo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of carcinogenic signaling networks in endometrial cancer identifies RAB17 as a potential target</atitle><jtitle>Journal of cellular physiology</jtitle><date>2021-01</date><risdate>2021</risdate><volume>236</volume><issue>1</issue><spage>328</spage><epage>339</epage><pages>328-339</pages><issn>0021-9541</issn><eissn>1097-4652</eissn><abstract>Endometrial cancer is one of the most common malignancies in postmenopausal women. Several potential therapeutic targets have been investigated in current research, but few have been used clinically. Therefore, further investigating the potential pathogenesis of endometrial cancer and new effective therapeutic targets for endometrial malignancies is still necessary. Our study used a The Cancer Genome Atlas dataset and two Gene Expression Omnibus datasets for weighted gene coexpression network analysis to identify important genes associated with the histological grades of endometrial cancer. In addition, we performed gene set enrichment analysis on the three datasets and found that abnormally activated signaling pathways and metabolic pathways are the main biological behaviors of endometrial cancer. Moreover, we further used different algorithms and identified the RAB17 gene as a potential study object. To further illustrate the potential role of the genes we analyzed in clinical and cellular aspects, we performed a clinical correlation analysis. Finally, we demonstrated the important roles and mechanisms of the RAB17 gene in the cell cycle, proliferation, and metastasis of endometrial cancer. Using repeated database analysis and cell‐level assays, we propose RAB17 as a potential target gene for endometrial cancer for further study.
We demonstrated the important roles and mechanisms of the RAB17 gene in the cell cycle, proliferation, and metastasis of endometrial cancer. Using repeated database analysis and cell‐level assays, we propose RAB17 as a potential target gene for endometrial cancer for further study.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/jcp.29845</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-4783-4120</orcidid></addata></record> |
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subjects | Algorithms Cancer Carcinogens Cell cycle Correlation analysis Datasets Endometrial cancer Endometrium Gene expression Gene set enrichment analysis Genes Genomes Metabolic pathways Metastases metastasis Network analysis Pathogenesis Post-menopause proliferation RAB17 Signal transduction Signaling Therapeutic applications WGCNA |
title | Analysis of carcinogenic signaling networks in endometrial cancer identifies RAB17 as a potential target |
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