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Bioinformatics analysis of GPS1 expression and biological function in breast cancer
G protein pathway suppressor 1 (GPS1) is involved in the development of many diseases including tumors, but its specific regulatory mechanism in breast cancer is not clear. The goal of the present study was to explore the biological effects and underlying mechanism of GPS1 in breast cancer. Public d...
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Published in: | Journal of cancer research and clinical oncology 2024-01, Vol.150 (2), p.52-52, Article 52 |
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description | G protein pathway suppressor 1 (GPS1) is involved in the development of many diseases including tumors, but its specific regulatory mechanism in breast cancer is not clear. The goal of the present study was to explore the biological effects and underlying mechanism of GPS1 in breast cancer. Public databases were used to analyze GPS1 expression and the relationship with clinicopathological characteristics and prognosis of breast cancer patients, combined with in vitro experiments to analyze the mechanism of action and immune relevance of GPS1 in breast cancer. Data analysis showed that the expression of GPS1 in breast cancer tissues was significantly higher than that in paracancerous tissues (
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doi_str_mv | 10.1007/s00432-023-05569-2 |
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p
< 0.001), and the receiver operating curve (ROC) revealed a higher diagnostic efficiency (AUC = 0.832). Survival analyses indicated that patients with high GPS1 expression made the prognosis worse in Luminal B, low to intermediate-grade breast cancers. Enrichment analysis showed that GPS1 was involved in the formation of ribonucleoprotein complexes, which dynamically altered the fate of RNA; it could also enhance the responsiveness of the Wnt pathway by interacting with WBP2. In addition, GPS1 expression was closely related to the immune microenvironment. GPS1 knockdown inhibits the proliferation, invasion and migration of MCF7 and MDA-MB-231 cells in vitro. This study suggests that the upregulation of GPS1 is associated with the malignant biological behavior and prognosis of breast cancer and may promote cancer progression. The correlation between GPS1 and the immune microenvironment suggests that it may be a potential target for immunotherapy.</description><identifier>ISSN: 1432-1335</identifier><identifier>ISSN: 0171-5216</identifier><identifier>EISSN: 1432-1335</identifier><identifier>DOI: 10.1007/s00432-023-05569-2</identifier><identifier>PMID: 38289496</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Bioinformatics ; Breast ; Breast cancer ; breast neoplasms ; Breast Neoplasms - genetics ; breasts ; Cancer Research ; Cell proliferation ; Computational Biology ; COP9 Signalosome Complex - genetics ; Databases, Factual ; Female ; Hematology ; Humans ; Immunotherapy ; Internal Medicine ; mechanism of action ; Medical prognosis ; Medicine ; Medicine & Public Health ; Microenvironments ; neoplasm progression ; Oncology ; Prognosis ; ribonucleoproteins ; RNA ; Trans-Activators ; Tumor Microenvironment ; Wnt protein</subject><ispartof>Journal of cancer research and clinical oncology, 2024-01, Vol.150 (2), p.52-52, Article 52</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c487t-3fbcc69a11096367c03c9f85655e61734446cca8937075b6718b71d0d7973ecb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38289496$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wei, Hong</creatorcontrib><creatorcontrib>Niu, Zhaocan</creatorcontrib><creatorcontrib>Ji, Ruixue</creatorcontrib><creatorcontrib>Jiang, Wenwen</creatorcontrib><creatorcontrib>Tang, Jiawei</creatorcontrib><creatorcontrib>Meng, Zhexuan</creatorcontrib><creatorcontrib>Cao, Xiaoyang</creatorcontrib><creatorcontrib>Zhang, Xinyi</creatorcontrib><creatorcontrib>Liu, Xue</creatorcontrib><title>Bioinformatics analysis of GPS1 expression and biological function in breast cancer</title><title>Journal of cancer research and clinical oncology</title><addtitle>J Cancer Res Clin Oncol</addtitle><addtitle>J Cancer Res Clin Oncol</addtitle><description>G protein pathway suppressor 1 (GPS1) is involved in the development of many diseases including tumors, but its specific regulatory mechanism in breast cancer is not clear. The goal of the present study was to explore the biological effects and underlying mechanism of GPS1 in breast cancer. Public databases were used to analyze GPS1 expression and the relationship with clinicopathological characteristics and prognosis of breast cancer patients, combined with in vitro experiments to analyze the mechanism of action and immune relevance of GPS1 in breast cancer. Data analysis showed that the expression of GPS1 in breast cancer tissues was significantly higher than that in paracancerous tissues (
p
< 0.001), and the receiver operating curve (ROC) revealed a higher diagnostic efficiency (AUC = 0.832). Survival analyses indicated that patients with high GPS1 expression made the prognosis worse in Luminal B, low to intermediate-grade breast cancers. Enrichment analysis showed that GPS1 was involved in the formation of ribonucleoprotein complexes, which dynamically altered the fate of RNA; it could also enhance the responsiveness of the Wnt pathway by interacting with WBP2. In addition, GPS1 expression was closely related to the immune microenvironment. GPS1 knockdown inhibits the proliferation, invasion and migration of MCF7 and MDA-MB-231 cells in vitro. This study suggests that the upregulation of GPS1 is associated with the malignant biological behavior and prognosis of breast cancer and may promote cancer progression. The correlation between GPS1 and the immune microenvironment suggests that it may be a potential target for immunotherapy.</description><subject>Bioinformatics</subject><subject>Breast</subject><subject>Breast cancer</subject><subject>breast neoplasms</subject><subject>Breast Neoplasms - genetics</subject><subject>breasts</subject><subject>Cancer Research</subject><subject>Cell proliferation</subject><subject>Computational Biology</subject><subject>COP9 Signalosome Complex - genetics</subject><subject>Databases, Factual</subject><subject>Female</subject><subject>Hematology</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Internal Medicine</subject><subject>mechanism of action</subject><subject>Medical prognosis</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Microenvironments</subject><subject>neoplasm progression</subject><subject>Oncology</subject><subject>Prognosis</subject><subject>ribonucleoproteins</subject><subject>RNA</subject><subject>Trans-Activators</subject><subject>Tumor Microenvironment</subject><subject>Wnt protein</subject><issn>1432-1335</issn><issn>0171-5216</issn><issn>1432-1335</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkk9PFTEUxRsjEUS_gAsziRs2I_f2f1dGCaIJiSbouun0dZ4l89pnO2Pg2zPDQ0QXsmpzz6_ntreHkFcIbxFAHVcAzmgLlLUghDQtfUIOcCkhY-Lpg_0-eV7rJQAqoegzss801YYbeUAuPsQcU5_Lxo3R18YlN1zXWJvcN2dfL7AJV9sSao05zdqq6WIe8jp6NzT9lPy41GNquhJcHRvvkg_lBdnr3VDDy7v1kHz_ePrt5FN7_uXs88n789ZzrcaW9Z330jhEMJJJ5YF502shhQgSFeOcS--dNkyBEp1UqDuFK1gpo1jwHTsk73a-26nbhJUPaSxusNsSN65c2-yi_VtJ8Ydd518WQdPZhM8OR3cOJf-cQh3tJlYfhsGlkKdqGQomgXFKH0WpoYBazs4z-uYf9DJPZR7sLSWUVMDxEQqpRqMXiu4oX3KtJfT3z0OwSwrsLgV2ToG9TYFdLvD64WDuj_z-9hlgO6DOUlqH8qf3f2xvAETru1Y</recordid><startdate>20240130</startdate><enddate>20240130</enddate><creator>Wei, Hong</creator><creator>Niu, Zhaocan</creator><creator>Ji, Ruixue</creator><creator>Jiang, Wenwen</creator><creator>Tang, Jiawei</creator><creator>Meng, Zhexuan</creator><creator>Cao, Xiaoyang</creator><creator>Zhang, Xinyi</creator><creator>Liu, Xue</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20240130</creationdate><title>Bioinformatics analysis of GPS1 expression and biological function in breast cancer</title><author>Wei, Hong ; Niu, Zhaocan ; Ji, Ruixue ; Jiang, Wenwen ; Tang, Jiawei ; Meng, Zhexuan ; Cao, Xiaoyang ; Zhang, Xinyi ; Liu, Xue</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c487t-3fbcc69a11096367c03c9f85655e61734446cca8937075b6718b71d0d7973ecb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Bioinformatics</topic><topic>Breast</topic><topic>Breast cancer</topic><topic>breast neoplasms</topic><topic>Breast Neoplasms - 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Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of cancer research and clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wei, Hong</au><au>Niu, Zhaocan</au><au>Ji, Ruixue</au><au>Jiang, Wenwen</au><au>Tang, Jiawei</au><au>Meng, Zhexuan</au><au>Cao, Xiaoyang</au><au>Zhang, Xinyi</au><au>Liu, Xue</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bioinformatics analysis of GPS1 expression and biological function in breast cancer</atitle><jtitle>Journal of cancer research and clinical oncology</jtitle><stitle>J Cancer Res Clin Oncol</stitle><addtitle>J Cancer Res Clin Oncol</addtitle><date>2024-01-30</date><risdate>2024</risdate><volume>150</volume><issue>2</issue><spage>52</spage><epage>52</epage><pages>52-52</pages><artnum>52</artnum><issn>1432-1335</issn><issn>0171-5216</issn><eissn>1432-1335</eissn><abstract>G protein pathway suppressor 1 (GPS1) is involved in the development of many diseases including tumors, but its specific regulatory mechanism in breast cancer is not clear. The goal of the present study was to explore the biological effects and underlying mechanism of GPS1 in breast cancer. Public databases were used to analyze GPS1 expression and the relationship with clinicopathological characteristics and prognosis of breast cancer patients, combined with in vitro experiments to analyze the mechanism of action and immune relevance of GPS1 in breast cancer. Data analysis showed that the expression of GPS1 in breast cancer tissues was significantly higher than that in paracancerous tissues (
p
< 0.001), and the receiver operating curve (ROC) revealed a higher diagnostic efficiency (AUC = 0.832). Survival analyses indicated that patients with high GPS1 expression made the prognosis worse in Luminal B, low to intermediate-grade breast cancers. Enrichment analysis showed that GPS1 was involved in the formation of ribonucleoprotein complexes, which dynamically altered the fate of RNA; it could also enhance the responsiveness of the Wnt pathway by interacting with WBP2. In addition, GPS1 expression was closely related to the immune microenvironment. GPS1 knockdown inhibits the proliferation, invasion and migration of MCF7 and MDA-MB-231 cells in vitro. This study suggests that the upregulation of GPS1 is associated with the malignant biological behavior and prognosis of breast cancer and may promote cancer progression. The correlation between GPS1 and the immune microenvironment suggests that it may be a potential target for immunotherapy.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>38289496</pmid><doi>10.1007/s00432-023-05569-2</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bioinformatics Breast Breast cancer breast neoplasms Breast Neoplasms - genetics breasts Cancer Research Cell proliferation Computational Biology COP9 Signalosome Complex - genetics Databases, Factual Female Hematology Humans Immunotherapy Internal Medicine mechanism of action Medical prognosis Medicine Medicine & Public Health Microenvironments neoplasm progression Oncology Prognosis ribonucleoproteins RNA Trans-Activators Tumor Microenvironment Wnt protein |
title | Bioinformatics analysis of GPS1 expression and biological function in breast cancer |
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