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High Expression of ITGA3 Promotes Proliferation and Cell Cycle Progression and Indicates Poor Prognosis in Intrahepatic Cholangiocarcinoma
Integrin subunit alpha 3 (ITGA3) interacts with a beta 1 subunit to form a member of the integrin family. Integrins are heterodimeric integral membrane proteins that serve as cell surface adhesion proteins. In this research, we investigated the biological function of this protein in human intrahepat...
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Published in: | BioMed research international 2018-01, Vol.2018 (2018), p.1-9 |
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creator | Lu, Sinan Zhou, Lin Xie, Haiyang Zheng, Shusen Wang, Weilin Zhou, Dongkai Zhang, Linshi Yan, Yingcai Zhou, Xiaohu He, Tianyu Zhang, Lufei Kong, Yang Huang, Yu Zhou, Jiarong |
description | Integrin subunit alpha 3 (ITGA3) interacts with a beta 1 subunit to form a member of the integrin family. Integrins are heterodimeric integral membrane proteins that serve as cell surface adhesion proteins. In this research, we investigated the biological function of this protein in human intrahepatic cholangiocarcinoma (ICC) for the first time. Here, using Western blotting and immunohistochemistry assays, we discovered that ITGA3 was overexpressed in ICC cell lines and ICC patients. Moreover, we found ITGA3 expression correlated with several clinicopathological features, including tumor size, lymph node metastasis, and the TNM stage. Patients with high ITGA3 expression underwent a worse prognosis after complete resection compared with patients with low ITGA3 expression in terms of overall survival. Furthermore, we demonstrated that ITGA3 could significantly promote ICC cell proliferation and cell cycle progression in vitro. However, as a classical cell surface adhesion molecule, we found ITGA3 correlated negatively with the migration and invasion of ICC cell lines, which differs from other malignant tumors. Generally, these findings suggest that ITGA3 may play a role as a potential oncogene in ICC and suppression of ITGA3 expression may establish a novel target for guiding the therapy of ICC patients. |
doi_str_mv | 10.1155/2018/2352139 |
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Integrins are heterodimeric integral membrane proteins that serve as cell surface adhesion proteins. In this research, we investigated the biological function of this protein in human intrahepatic cholangiocarcinoma (ICC) for the first time. Here, using Western blotting and immunohistochemistry assays, we discovered that ITGA3 was overexpressed in ICC cell lines and ICC patients. Moreover, we found ITGA3 expression correlated with several clinicopathological features, including tumor size, lymph node metastasis, and the TNM stage. Patients with high ITGA3 expression underwent a worse prognosis after complete resection compared with patients with low ITGA3 expression in terms of overall survival. Furthermore, we demonstrated that ITGA3 could significantly promote ICC cell proliferation and cell cycle progression in vitro. However, as a classical cell surface adhesion molecule, we found ITGA3 correlated negatively with the migration and invasion of ICC cell lines, which differs from other malignant tumors. Generally, these findings suggest that ITGA3 may play a role as a potential oncogene in ICC and suppression of ITGA3 expression may establish a novel target for guiding the therapy of ICC patients.</description><identifier>ISSN: 2314-6133</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2018/2352139</identifier><identifier>PMID: 29511671</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Adhesion ; Biotechnology ; Cancer therapies ; Cell culture ; Cell cycle ; Cell proliferation ; Cell surface ; Cholangiocarcinoma ; Extracellular matrix ; Hospitals ; Immunohistochemistry ; Integral membrane proteins ; Integrins ; Laboratories ; Liver cancer ; Lymph nodes ; Medical diagnosis ; Medical prognosis ; Medicine ; Melanoma ; Membrane proteins ; Metastases ; Metastasis ; MicroRNAs ; Patients ; Prognosis ; Prostate cancer ; Proteins ; Rodents ; Surgery ; Surgical outcomes ; Tumors ; Western blotting</subject><ispartof>BioMed research international, 2018-01, Vol.2018 (2018), p.1-9</ispartof><rights>Copyright © 2018 Yu Huang et al.</rights><rights>COPYRIGHT 2018 John Wiley & Sons, Inc.</rights><rights>Copyright © 2018 Yu Huang et al.; This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2018 Yu Huang et al. 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-bc2a1c7bc3fb4047d7e6a3349a66510cea05dddc995b45aede67f414f37104903</citedby><cites>FETCH-LOGICAL-c499t-bc2a1c7bc3fb4047d7e6a3349a66510cea05dddc995b45aede67f414f37104903</cites><orcidid>0000-0003-1459-8261 ; 0000-0001-9432-2649 ; 0000-0002-6270-0737</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2002928552/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2002928552?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,25731,27901,27902,36989,36990,44566,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29511671$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Aishima, Shinichi</contributor><creatorcontrib>Lu, Sinan</creatorcontrib><creatorcontrib>Zhou, Lin</creatorcontrib><creatorcontrib>Xie, Haiyang</creatorcontrib><creatorcontrib>Zheng, Shusen</creatorcontrib><creatorcontrib>Wang, Weilin</creatorcontrib><creatorcontrib>Zhou, Dongkai</creatorcontrib><creatorcontrib>Zhang, Linshi</creatorcontrib><creatorcontrib>Yan, Yingcai</creatorcontrib><creatorcontrib>Zhou, Xiaohu</creatorcontrib><creatorcontrib>He, Tianyu</creatorcontrib><creatorcontrib>Zhang, Lufei</creatorcontrib><creatorcontrib>Kong, Yang</creatorcontrib><creatorcontrib>Huang, Yu</creatorcontrib><creatorcontrib>Zhou, Jiarong</creatorcontrib><title>High Expression of ITGA3 Promotes Proliferation and Cell Cycle Progression and Indicates Poor Prognosis in Intrahepatic Cholangiocarcinoma</title><title>BioMed research international</title><addtitle>Biomed Res Int</addtitle><description>Integrin subunit alpha 3 (ITGA3) interacts with a beta 1 subunit to form a member of the integrin family. Integrins are heterodimeric integral membrane proteins that serve as cell surface adhesion proteins. In this research, we investigated the biological function of this protein in human intrahepatic cholangiocarcinoma (ICC) for the first time. Here, using Western blotting and immunohistochemistry assays, we discovered that ITGA3 was overexpressed in ICC cell lines and ICC patients. Moreover, we found ITGA3 expression correlated with several clinicopathological features, including tumor size, lymph node metastasis, and the TNM stage. Patients with high ITGA3 expression underwent a worse prognosis after complete resection compared with patients with low ITGA3 expression in terms of overall survival. Furthermore, we demonstrated that ITGA3 could significantly promote ICC cell proliferation and cell cycle progression in vitro. However, as a classical cell surface adhesion molecule, we found ITGA3 correlated negatively with the migration and invasion of ICC cell lines, which differs from other malignant tumors. Generally, these findings suggest that ITGA3 may play a role as a potential oncogene in ICC and suppression of ITGA3 expression may establish a novel target for guiding the therapy of ICC patients.</description><subject>Adhesion</subject><subject>Biotechnology</subject><subject>Cancer therapies</subject><subject>Cell culture</subject><subject>Cell cycle</subject><subject>Cell proliferation</subject><subject>Cell surface</subject><subject>Cholangiocarcinoma</subject><subject>Extracellular matrix</subject><subject>Hospitals</subject><subject>Immunohistochemistry</subject><subject>Integral membrane proteins</subject><subject>Integrins</subject><subject>Laboratories</subject><subject>Liver cancer</subject><subject>Lymph nodes</subject><subject>Medical diagnosis</subject><subject>Medical prognosis</subject><subject>Medicine</subject><subject>Melanoma</subject><subject>Membrane proteins</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>MicroRNAs</subject><subject>Patients</subject><subject>Prognosis</subject><subject>Prostate cancer</subject><subject>Proteins</subject><subject>Rodents</subject><subject>Surgery</subject><subject>Surgical outcomes</subject><subject>Tumors</subject><subject>Western 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Expression of ITGA3 Promotes Proliferation and Cell Cycle Progression and Indicates Poor Prognosis in Intrahepatic Cholangiocarcinoma</title><author>Lu, Sinan ; Zhou, Lin ; Xie, Haiyang ; Zheng, Shusen ; Wang, Weilin ; Zhou, Dongkai ; Zhang, Linshi ; Yan, Yingcai ; Zhou, Xiaohu ; He, Tianyu ; Zhang, Lufei ; Kong, Yang ; Huang, Yu ; Zhou, Jiarong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c499t-bc2a1c7bc3fb4047d7e6a3349a66510cea05dddc995b45aede67f414f37104903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adhesion</topic><topic>Biotechnology</topic><topic>Cancer therapies</topic><topic>Cell culture</topic><topic>Cell cycle</topic><topic>Cell proliferation</topic><topic>Cell surface</topic><topic>Cholangiocarcinoma</topic><topic>Extracellular matrix</topic><topic>Hospitals</topic><topic>Immunohistochemistry</topic><topic>Integral membrane 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Sinan</au><au>Zhou, Lin</au><au>Xie, Haiyang</au><au>Zheng, Shusen</au><au>Wang, Weilin</au><au>Zhou, Dongkai</au><au>Zhang, Linshi</au><au>Yan, Yingcai</au><au>Zhou, Xiaohu</au><au>He, Tianyu</au><au>Zhang, Lufei</au><au>Kong, Yang</au><au>Huang, Yu</au><au>Zhou, Jiarong</au><au>Aishima, Shinichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High Expression of ITGA3 Promotes Proliferation and Cell Cycle Progression and Indicates Poor Prognosis in Intrahepatic Cholangiocarcinoma</atitle><jtitle>BioMed research international</jtitle><addtitle>Biomed Res Int</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>2018</volume><issue>2018</issue><spage>1</spage><epage>9</epage><pages>1-9</pages><issn>2314-6133</issn><eissn>2314-6141</eissn><abstract>Integrin subunit alpha 3 (ITGA3) interacts with a beta 1 subunit to form a member of the integrin family. Integrins are heterodimeric integral membrane proteins that serve as cell surface adhesion proteins. In this research, we investigated the biological function of this protein in human intrahepatic cholangiocarcinoma (ICC) for the first time. Here, using Western blotting and immunohistochemistry assays, we discovered that ITGA3 was overexpressed in ICC cell lines and ICC patients. Moreover, we found ITGA3 expression correlated with several clinicopathological features, including tumor size, lymph node metastasis, and the TNM stage. Patients with high ITGA3 expression underwent a worse prognosis after complete resection compared with patients with low ITGA3 expression in terms of overall survival. Furthermore, we demonstrated that ITGA3 could significantly promote ICC cell proliferation and cell cycle progression in vitro. However, as a classical cell surface adhesion molecule, we found ITGA3 correlated negatively with the migration and invasion of ICC cell lines, which differs from other malignant tumors. Generally, these findings suggest that ITGA3 may play a role as a potential oncogene in ICC and suppression of ITGA3 expression may establish a novel target for guiding the therapy of ICC patients.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>29511671</pmid><doi>10.1155/2018/2352139</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-1459-8261</orcidid><orcidid>https://orcid.org/0000-0001-9432-2649</orcidid><orcidid>https://orcid.org/0000-0002-6270-0737</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adhesion Biotechnology Cancer therapies Cell culture Cell cycle Cell proliferation Cell surface Cholangiocarcinoma Extracellular matrix Hospitals Immunohistochemistry Integral membrane proteins Integrins Laboratories Liver cancer Lymph nodes Medical diagnosis Medical prognosis Medicine Melanoma Membrane proteins Metastases Metastasis MicroRNAs Patients Prognosis Prostate cancer Proteins Rodents Surgery Surgical outcomes Tumors Western blotting |
title | High Expression of ITGA3 Promotes Proliferation and Cell Cycle Progression and Indicates Poor Prognosis in Intrahepatic Cholangiocarcinoma |
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