Global expression profiling and pathway analysis of mouse mammary tumor reveals strain and stage specific dysregulated pathways in breast cancer progression

It is believed that the alteration of tissue microenvironment would affect cancer initiation and progression. However, little is known in terms of the underlying molecular mechanisms that would affect the initiation and progression of breast cancer. In the present study, we use two murine mammary tu...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cell cycle (Georgetown, Tex.) Tex.), 2018-04, Vol.17 (8), p.963-973
Hauptverfasser: Mei, Yan, Yang, Jun-Ping, Lang, Yan-Hong, Peng, Li-Xia, Yang, Ming-Ming, Liu, Qing, Meng, Dong-Fang, Zheng, Li-Sheng, Qiang, Yuan-Yuan, Xu, Liang, Li, Chang-Zhi, Wei, Wen-Wen, Niu, Ting, Peng, Xing-Si, Yang, Qin, Lin, Fen, Hu, Hao, Xu, Hong-Fa, Huang, Bi-Jun, Wang, Li-Jing, Qian, Chao-Nan
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 973
container_issue 8
container_start_page 963
container_title Cell cycle (Georgetown, Tex.)
container_volume 17
creator Mei, Yan
Yang, Jun-Ping
Lang, Yan-Hong
Peng, Li-Xia
Yang, Ming-Ming
Liu, Qing
Meng, Dong-Fang
Zheng, Li-Sheng
Qiang, Yuan-Yuan
Xu, Liang
Li, Chang-Zhi
Wei, Wen-Wen
Niu, Ting
Peng, Xing-Si
Yang, Qin
Lin, Fen
Hu, Hao
Xu, Hong-Fa
Huang, Bi-Jun
Wang, Li-Jing
Qian, Chao-Nan
description It is believed that the alteration of tissue microenvironment would affect cancer initiation and progression. However, little is known in terms of the underlying molecular mechanisms that would affect the initiation and progression of breast cancer. In the present study, we use two murine mammary tumor models with different speeds of tumor initiation and progression for whole genome expression profiling to reveal the involved genes and signaling pathways. The pathways regulating PI3K-Akt signaling and Ras signaling were activated in Fvb mice and promoted tumor progression. Contrastingly, the pathways regulating apoptosis and cellular senescence were activated in Fvb.B6 mice and suppressed tumor progression. We identified distinct patterns of oncogenic pathways activation at different stages of breast cancer, and uncovered five oncogenic pathways that were activated in both human and mouse breast cancers. The genes and pathways discovered in our study would be useful information for other researchers and drug development.
doi_str_mv 10.1080/15384101.2018.1442629
format Article
fullrecord <record><control><sourceid>proquest_infor</sourceid><recordid>TN_cdi_proquest_miscellaneous_2033389552</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2033389552</sourcerecordid><originalsourceid>FETCH-LOGICAL-c468t-26c621f48dee0b1cca4b9af3c6c49a8f7dcf4a3a9667734b988805bdda2913633</originalsourceid><addsrcrecordid>eNp9Uctu1TAQjRCIPuATQF6yycWP2HE2CFS1BakSG1hbE8dOjZw42ElL_oWPxem9vaKbrmakOefMzDlF8Y7gHcESfyScyYpgsqOYyB2pKipo86I4JZyTssKYv9x6JssNdFKcpfQLYyrrhrwuTmhTE8pZfVr8vfahBY_MnymalFwY0RSDdd6NPYKxQxPMt_ew5h78mlxCwaIhLMmgAYYB4ormZQgRRXNnwCeU5ghufKCmGXqD0mS0s06jbk3R9IuH2RxlE8rYNhpIM9IwahO39f3hlDfFK5s1zdtDPS9-Xl3-uPha3ny__nbx5abUlZBzSYUWlNhKdsbglmgNVduAZVroqgFp607bChg0QtQ1yzMpJeZt1wFtCBOMnRef9rrT0g6m02bMT3g1Rbc9qAI49XQyulvVhzslCGaCN1ngw0Eght-LSbMaXNLGexhN9kpRzBiTDec0Q_keqmNI2RB7XEOw2pJVj8mqLVl1SDbz3v9_45H1GGUGfN4D3GhDHOA-RN-pGVYfoo3ZW5cUe37HP78_uP8</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2033389552</pqid></control><display><type>article</type><title>Global expression profiling and pathway analysis of mouse mammary tumor reveals strain and stage specific dysregulated pathways in breast cancer progression</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Mei, Yan ; Yang, Jun-Ping ; Lang, Yan-Hong ; Peng, Li-Xia ; Yang, Ming-Ming ; Liu, Qing ; Meng, Dong-Fang ; Zheng, Li-Sheng ; Qiang, Yuan-Yuan ; Xu, Liang ; Li, Chang-Zhi ; Wei, Wen-Wen ; Niu, Ting ; Peng, Xing-Si ; Yang, Qin ; Lin, Fen ; Hu, Hao ; Xu, Hong-Fa ; Huang, Bi-Jun ; Wang, Li-Jing ; Qian, Chao-Nan</creator><creatorcontrib>Mei, Yan ; Yang, Jun-Ping ; Lang, Yan-Hong ; Peng, Li-Xia ; Yang, Ming-Ming ; Liu, Qing ; Meng, Dong-Fang ; Zheng, Li-Sheng ; Qiang, Yuan-Yuan ; Xu, Liang ; Li, Chang-Zhi ; Wei, Wen-Wen ; Niu, Ting ; Peng, Xing-Si ; Yang, Qin ; Lin, Fen ; Hu, Hao ; Xu, Hong-Fa ; Huang, Bi-Jun ; Wang, Li-Jing ; Qian, Chao-Nan</creatorcontrib><description>It is believed that the alteration of tissue microenvironment would affect cancer initiation and progression. However, little is known in terms of the underlying molecular mechanisms that would affect the initiation and progression of breast cancer. In the present study, we use two murine mammary tumor models with different speeds of tumor initiation and progression for whole genome expression profiling to reveal the involved genes and signaling pathways. The pathways regulating PI3K-Akt signaling and Ras signaling were activated in Fvb mice and promoted tumor progression. Contrastingly, the pathways regulating apoptosis and cellular senescence were activated in Fvb.B6 mice and suppressed tumor progression. We identified distinct patterns of oncogenic pathways activation at different stages of breast cancer, and uncovered five oncogenic pathways that were activated in both human and mouse breast cancers. The genes and pathways discovered in our study would be useful information for other researchers and drug development.</description><identifier>ISSN: 1538-4101</identifier><identifier>EISSN: 1551-4005</identifier><identifier>DOI: 10.1080/15384101.2018.1442629</identifier><identifier>PMID: 29712537</identifier><language>eng</language><publisher>United States: Taylor &amp; Francis</publisher><subject>Apoptosis ; Breast cancer ; Cancer progression ; PI3K-Akt signaling ; Ras signaling ; RNA-sequencing</subject><ispartof>Cell cycle (Georgetown, Tex.), 2018-04, Vol.17 (8), p.963-973</ispartof><rights>2018 Taylor &amp; Francis 2018</rights><rights>2018 Taylor &amp; Francis 2018 Taylor &amp; Francis</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-26c621f48dee0b1cca4b9af3c6c49a8f7dcf4a3a9667734b988805bdda2913633</citedby><cites>FETCH-LOGICAL-c468t-26c621f48dee0b1cca4b9af3c6c49a8f7dcf4a3a9667734b988805bdda2913633</cites><orcidid>0000-0002-4292-1006</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103659/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103659/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29712537$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mei, Yan</creatorcontrib><creatorcontrib>Yang, Jun-Ping</creatorcontrib><creatorcontrib>Lang, Yan-Hong</creatorcontrib><creatorcontrib>Peng, Li-Xia</creatorcontrib><creatorcontrib>Yang, Ming-Ming</creatorcontrib><creatorcontrib>Liu, Qing</creatorcontrib><creatorcontrib>Meng, Dong-Fang</creatorcontrib><creatorcontrib>Zheng, Li-Sheng</creatorcontrib><creatorcontrib>Qiang, Yuan-Yuan</creatorcontrib><creatorcontrib>Xu, Liang</creatorcontrib><creatorcontrib>Li, Chang-Zhi</creatorcontrib><creatorcontrib>Wei, Wen-Wen</creatorcontrib><creatorcontrib>Niu, Ting</creatorcontrib><creatorcontrib>Peng, Xing-Si</creatorcontrib><creatorcontrib>Yang, Qin</creatorcontrib><creatorcontrib>Lin, Fen</creatorcontrib><creatorcontrib>Hu, Hao</creatorcontrib><creatorcontrib>Xu, Hong-Fa</creatorcontrib><creatorcontrib>Huang, Bi-Jun</creatorcontrib><creatorcontrib>Wang, Li-Jing</creatorcontrib><creatorcontrib>Qian, Chao-Nan</creatorcontrib><title>Global expression profiling and pathway analysis of mouse mammary tumor reveals strain and stage specific dysregulated pathways in breast cancer progression</title><title>Cell cycle (Georgetown, Tex.)</title><addtitle>Cell Cycle</addtitle><description>It is believed that the alteration of tissue microenvironment would affect cancer initiation and progression. However, little is known in terms of the underlying molecular mechanisms that would affect the initiation and progression of breast cancer. In the present study, we use two murine mammary tumor models with different speeds of tumor initiation and progression for whole genome expression profiling to reveal the involved genes and signaling pathways. The pathways regulating PI3K-Akt signaling and Ras signaling were activated in Fvb mice and promoted tumor progression. Contrastingly, the pathways regulating apoptosis and cellular senescence were activated in Fvb.B6 mice and suppressed tumor progression. We identified distinct patterns of oncogenic pathways activation at different stages of breast cancer, and uncovered five oncogenic pathways that were activated in both human and mouse breast cancers. The genes and pathways discovered in our study would be useful information for other researchers and drug development.</description><subject>Apoptosis</subject><subject>Breast cancer</subject><subject>Cancer progression</subject><subject>PI3K-Akt signaling</subject><subject>Ras signaling</subject><subject>RNA-sequencing</subject><issn>1538-4101</issn><issn>1551-4005</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9Uctu1TAQjRCIPuATQF6yycWP2HE2CFS1BakSG1hbE8dOjZw42ElL_oWPxem9vaKbrmakOefMzDlF8Y7gHcESfyScyYpgsqOYyB2pKipo86I4JZyTssKYv9x6JssNdFKcpfQLYyrrhrwuTmhTE8pZfVr8vfahBY_MnymalFwY0RSDdd6NPYKxQxPMt_ew5h78mlxCwaIhLMmgAYYB4ormZQgRRXNnwCeU5ghufKCmGXqD0mS0s06jbk3R9IuH2RxlE8rYNhpIM9IwahO39f3hlDfFK5s1zdtDPS9-Xl3-uPha3ny__nbx5abUlZBzSYUWlNhKdsbglmgNVduAZVroqgFp607bChg0QtQ1yzMpJeZt1wFtCBOMnRef9rrT0g6m02bMT3g1Rbc9qAI49XQyulvVhzslCGaCN1ngw0Eght-LSbMaXNLGexhN9kpRzBiTDec0Q_keqmNI2RB7XEOw2pJVj8mqLVl1SDbz3v9_45H1GGUGfN4D3GhDHOA-RN-pGVYfoo3ZW5cUe37HP78_uP8</recordid><startdate>20180418</startdate><enddate>20180418</enddate><creator>Mei, Yan</creator><creator>Yang, Jun-Ping</creator><creator>Lang, Yan-Hong</creator><creator>Peng, Li-Xia</creator><creator>Yang, Ming-Ming</creator><creator>Liu, Qing</creator><creator>Meng, Dong-Fang</creator><creator>Zheng, Li-Sheng</creator><creator>Qiang, Yuan-Yuan</creator><creator>Xu, Liang</creator><creator>Li, Chang-Zhi</creator><creator>Wei, Wen-Wen</creator><creator>Niu, Ting</creator><creator>Peng, Xing-Si</creator><creator>Yang, Qin</creator><creator>Lin, Fen</creator><creator>Hu, Hao</creator><creator>Xu, Hong-Fa</creator><creator>Huang, Bi-Jun</creator><creator>Wang, Li-Jing</creator><creator>Qian, Chao-Nan</creator><general>Taylor &amp; Francis</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4292-1006</orcidid></search><sort><creationdate>20180418</creationdate><title>Global expression profiling and pathway analysis of mouse mammary tumor reveals strain and stage specific dysregulated pathways in breast cancer progression</title><author>Mei, Yan ; Yang, Jun-Ping ; Lang, Yan-Hong ; Peng, Li-Xia ; Yang, Ming-Ming ; Liu, Qing ; Meng, Dong-Fang ; Zheng, Li-Sheng ; Qiang, Yuan-Yuan ; Xu, Liang ; Li, Chang-Zhi ; Wei, Wen-Wen ; Niu, Ting ; Peng, Xing-Si ; Yang, Qin ; Lin, Fen ; Hu, Hao ; Xu, Hong-Fa ; Huang, Bi-Jun ; Wang, Li-Jing ; Qian, Chao-Nan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-26c621f48dee0b1cca4b9af3c6c49a8f7dcf4a3a9667734b988805bdda2913633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Apoptosis</topic><topic>Breast cancer</topic><topic>Cancer progression</topic><topic>PI3K-Akt signaling</topic><topic>Ras signaling</topic><topic>RNA-sequencing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mei, Yan</creatorcontrib><creatorcontrib>Yang, Jun-Ping</creatorcontrib><creatorcontrib>Lang, Yan-Hong</creatorcontrib><creatorcontrib>Peng, Li-Xia</creatorcontrib><creatorcontrib>Yang, Ming-Ming</creatorcontrib><creatorcontrib>Liu, Qing</creatorcontrib><creatorcontrib>Meng, Dong-Fang</creatorcontrib><creatorcontrib>Zheng, Li-Sheng</creatorcontrib><creatorcontrib>Qiang, Yuan-Yuan</creatorcontrib><creatorcontrib>Xu, Liang</creatorcontrib><creatorcontrib>Li, Chang-Zhi</creatorcontrib><creatorcontrib>Wei, Wen-Wen</creatorcontrib><creatorcontrib>Niu, Ting</creatorcontrib><creatorcontrib>Peng, Xing-Si</creatorcontrib><creatorcontrib>Yang, Qin</creatorcontrib><creatorcontrib>Lin, Fen</creatorcontrib><creatorcontrib>Hu, Hao</creatorcontrib><creatorcontrib>Xu, Hong-Fa</creatorcontrib><creatorcontrib>Huang, Bi-Jun</creatorcontrib><creatorcontrib>Wang, Li-Jing</creatorcontrib><creatorcontrib>Qian, Chao-Nan</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell cycle (Georgetown, Tex.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mei, Yan</au><au>Yang, Jun-Ping</au><au>Lang, Yan-Hong</au><au>Peng, Li-Xia</au><au>Yang, Ming-Ming</au><au>Liu, Qing</au><au>Meng, Dong-Fang</au><au>Zheng, Li-Sheng</au><au>Qiang, Yuan-Yuan</au><au>Xu, Liang</au><au>Li, Chang-Zhi</au><au>Wei, Wen-Wen</au><au>Niu, Ting</au><au>Peng, Xing-Si</au><au>Yang, Qin</au><au>Lin, Fen</au><au>Hu, Hao</au><au>Xu, Hong-Fa</au><au>Huang, Bi-Jun</au><au>Wang, Li-Jing</au><au>Qian, Chao-Nan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Global expression profiling and pathway analysis of mouse mammary tumor reveals strain and stage specific dysregulated pathways in breast cancer progression</atitle><jtitle>Cell cycle (Georgetown, Tex.)</jtitle><addtitle>Cell Cycle</addtitle><date>2018-04-18</date><risdate>2018</risdate><volume>17</volume><issue>8</issue><spage>963</spage><epage>973</epage><pages>963-973</pages><issn>1538-4101</issn><eissn>1551-4005</eissn><abstract>It is believed that the alteration of tissue microenvironment would affect cancer initiation and progression. However, little is known in terms of the underlying molecular mechanisms that would affect the initiation and progression of breast cancer. In the present study, we use two murine mammary tumor models with different speeds of tumor initiation and progression for whole genome expression profiling to reveal the involved genes and signaling pathways. The pathways regulating PI3K-Akt signaling and Ras signaling were activated in Fvb mice and promoted tumor progression. Contrastingly, the pathways regulating apoptosis and cellular senescence were activated in Fvb.B6 mice and suppressed tumor progression. We identified distinct patterns of oncogenic pathways activation at different stages of breast cancer, and uncovered five oncogenic pathways that were activated in both human and mouse breast cancers. The genes and pathways discovered in our study would be useful information for other researchers and drug development.</abstract><cop>United States</cop><pub>Taylor &amp; Francis</pub><pmid>29712537</pmid><doi>10.1080/15384101.2018.1442629</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-4292-1006</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1538-4101
ispartof Cell cycle (Georgetown, Tex.), 2018-04, Vol.17 (8), p.963-973
issn 1538-4101
1551-4005
language eng
recordid cdi_proquest_miscellaneous_2033389552
source Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Apoptosis
Breast cancer
Cancer progression
PI3K-Akt signaling
Ras signaling
RNA-sequencing
title Global expression profiling and pathway analysis of mouse mammary tumor reveals strain and stage specific dysregulated pathways in breast cancer progression
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-31T01%3A47%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_infor&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Global%20expression%20profiling%20and%20pathway%20analysis%20of%20mouse%20mammary%20tumor%20reveals%20strain%20and%20stage%20specific%20dysregulated%20pathways%20in%20breast%20cancer%20progression&rft.jtitle=Cell%20cycle%20(Georgetown,%20Tex.)&rft.au=Mei,%20Yan&rft.date=2018-04-18&rft.volume=17&rft.issue=8&rft.spage=963&rft.epage=973&rft.pages=963-973&rft.issn=1538-4101&rft.eissn=1551-4005&rft_id=info:doi/10.1080/15384101.2018.1442629&rft_dat=%3Cproquest_infor%3E2033389552%3C/proquest_infor%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2033389552&rft_id=info:pmid/29712537&rfr_iscdi=true