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PTPN9 induces cell apoptosis by mitigating the activation of Stat3 and acts as a tumor suppressor in colorectal cancer
Accumulating evidence has shown that protein tyrosine phosphatases (PTPs) are involved in regulating the transduction of many signaling pathways and play important roles in modulating the progression of some cancers, but the functions of PTPs in cancers have not been well elucidated until now. Here,...
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Published in: | Cancer management and research 2019-01, Vol.11, p.1309-1319 |
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container_title | Cancer management and research |
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creator | Wang, Dawei Cheng, Zhuoxin Zhao, Ming Jiao, Chengbin Meng, Qinghui Pan, Huayang Xie, Yu Li, Long Zhu, Yexing Wang, Wei Qu, Chunlei Liang, Deshen |
description | Accumulating evidence has shown that protein tyrosine phosphatases (PTPs) are involved in regulating the transduction of many signaling pathways and play important roles in modulating the progression of some cancers, but the functions of PTPs in cancers have not been well elucidated until now. Here, we aimed to identify the roles of protein tyrosine phosphatase nonreceptor type 9 (PTPN9), a cytoplasmic PTP, in the development of colorectal cancer and elucidate the regulatory mechanism involved.
Cell viability assessment, colony formation assay, caspase-3 and caspase-9 activity assay, real-time PCR, and Western blot analysis were applied.
Our results showed that PTPN9 expression was frequently downregulated in colorectal cancer tissues compared with adjacent normal tissues. Overexpression of PTPN9 mitigated cell growth and colony formation and induced cell apoptosis in colorectal cancer. Conversely, PTPN9 knockdown promoted cell growth and survival. Moreover, PTPN9 negatively regulated the activation of Stat3 and depressed its nuclear translocation in colorectal cancer. The effects of PTPN9 knockdown on cell apoptosis were attenuated by inhibition of the Stat3 pathway.
These results indicate that PTPN9 inhibits cell growth and survival by repressing the activation of Stat3 in colorectal cancer, which suggests an important underlying mechanism of regulating cell growth and provides a novel candidate therapeutic target for colorectal cancer. |
doi_str_mv | 10.2147/CMAR.S187001 |
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Cell viability assessment, colony formation assay, caspase-3 and caspase-9 activity assay, real-time PCR, and Western blot analysis were applied.
Our results showed that PTPN9 expression was frequently downregulated in colorectal cancer tissues compared with adjacent normal tissues. Overexpression of PTPN9 mitigated cell growth and colony formation and induced cell apoptosis in colorectal cancer. Conversely, PTPN9 knockdown promoted cell growth and survival. Moreover, PTPN9 negatively regulated the activation of Stat3 and depressed its nuclear translocation in colorectal cancer. The effects of PTPN9 knockdown on cell apoptosis were attenuated by inhibition of the Stat3 pathway.
These results indicate that PTPN9 inhibits cell growth and survival by repressing the activation of Stat3 in colorectal cancer, which suggests an important underlying mechanism of regulating cell growth and provides a novel candidate therapeutic target for colorectal cancer.</description><identifier>ISSN: 1179-1322</identifier><identifier>EISSN: 1179-1322</identifier><identifier>DOI: 10.2147/CMAR.S187001</identifier><identifier>PMID: 30804683</identifier><language>eng</language><publisher>New Zealand: Dove Medical Press Limited</publisher><subject>Analysis ; Apoptosis ; Breast cancer ; Cancer therapies ; Cell cycle ; Cell growth ; cell survival ; Cervical cancer ; Colorectal cancer ; Development and progression ; Gastric cancer ; Growth factors ; Health aspects ; Hospitals ; Laboratories ; Liver cancer ; Metastasis ; MicroRNAs ; Original Research ; Phosphatase ; Phosphatases ; Proteins ; PTPMeg2 ; PTPN9 ; Scientific equipment and supplies industry ; Stat3 ; Surgery ; Tumors ; Tyrosine</subject><ispartof>Cancer management and research, 2019-01, Vol.11, p.1309-1319</ispartof><rights>COPYRIGHT 2019 Dove Medical Press Limited</rights><rights>2019. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 Wang et al. This work is published and licensed by Dove Medical Press Limited 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c588t-f7ba86b6e0e27087ce4aff0038d3f2f87e37f067f2b4b63470f6c62d7dab864e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2224435974/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2224435974?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30804683$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Dawei</creatorcontrib><creatorcontrib>Cheng, Zhuoxin</creatorcontrib><creatorcontrib>Zhao, Ming</creatorcontrib><creatorcontrib>Jiao, Chengbin</creatorcontrib><creatorcontrib>Meng, Qinghui</creatorcontrib><creatorcontrib>Pan, Huayang</creatorcontrib><creatorcontrib>Xie, Yu</creatorcontrib><creatorcontrib>Li, Long</creatorcontrib><creatorcontrib>Zhu, Yexing</creatorcontrib><creatorcontrib>Wang, Wei</creatorcontrib><creatorcontrib>Qu, Chunlei</creatorcontrib><creatorcontrib>Liang, Deshen</creatorcontrib><title>PTPN9 induces cell apoptosis by mitigating the activation of Stat3 and acts as a tumor suppressor in colorectal cancer</title><title>Cancer management and research</title><addtitle>Cancer Manag Res</addtitle><description>Accumulating evidence has shown that protein tyrosine phosphatases (PTPs) are involved in regulating the transduction of many signaling pathways and play important roles in modulating the progression of some cancers, but the functions of PTPs in cancers have not been well elucidated until now. Here, we aimed to identify the roles of protein tyrosine phosphatase nonreceptor type 9 (PTPN9), a cytoplasmic PTP, in the development of colorectal cancer and elucidate the regulatory mechanism involved.
Cell viability assessment, colony formation assay, caspase-3 and caspase-9 activity assay, real-time PCR, and Western blot analysis were applied.
Our results showed that PTPN9 expression was frequently downregulated in colorectal cancer tissues compared with adjacent normal tissues. Overexpression of PTPN9 mitigated cell growth and colony formation and induced cell apoptosis in colorectal cancer. Conversely, PTPN9 knockdown promoted cell growth and survival. Moreover, PTPN9 negatively regulated the activation of Stat3 and depressed its nuclear translocation in colorectal cancer. The effects of PTPN9 knockdown on cell apoptosis were attenuated by inhibition of the Stat3 pathway.
These results indicate that PTPN9 inhibits cell growth and survival by repressing the activation of Stat3 in colorectal cancer, which suggests an important underlying mechanism of regulating cell growth and provides a novel candidate therapeutic target for colorectal cancer.</description><subject>Analysis</subject><subject>Apoptosis</subject><subject>Breast cancer</subject><subject>Cancer therapies</subject><subject>Cell cycle</subject><subject>Cell growth</subject><subject>cell survival</subject><subject>Cervical cancer</subject><subject>Colorectal cancer</subject><subject>Development and progression</subject><subject>Gastric cancer</subject><subject>Growth factors</subject><subject>Health aspects</subject><subject>Hospitals</subject><subject>Laboratories</subject><subject>Liver cancer</subject><subject>Metastasis</subject><subject>MicroRNAs</subject><subject>Original Research</subject><subject>Phosphatase</subject><subject>Phosphatases</subject><subject>Proteins</subject><subject>PTPMeg2</subject><subject>PTPN9</subject><subject>Scientific equipment and supplies industry</subject><subject>Stat3</subject><subject>Surgery</subject><subject>Tumors</subject><subject>Tyrosine</subject><issn>1179-1322</issn><issn>1179-1322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUk1rGzEQXUpLk7i99VwEvfQQu_qyJF8KxvQjkLahSc9Cqw9HZlfaSFpD_n3l2g12KRJoNHrzhnl6TfMGwRlGlH9YfVv-nN0iwSFEz5pzhPhiigjGz4_is-Yi5w2EbIEIfdmcESggZYKcN9ubu5vvC-CDGbXNQNuuA2qIQ4nZZ9A-gt4Xv1bFhzUo9xYoXfy2XmMA0YHbogoBKphdPgNVNyhjHxPI4zAkm3MNfQA6djFZXVQHtAraplfNC6e6bF8fzknz6_Onu9XX6fWPL1er5fVUz4UoU8dbJVjLLLSYQ8G1pco5CIkwxGEnuCXcQcYdbmnLCOXQMc2w4Ua1glFLJs3VntdEtZFD8r1KjzIqL_8kYlpLlYrXnZWUcYGp09RVbaDGihhCzdzMERXYGlK5Pu65hrHtrdE2lKS6E9LTl-Dv5TpuJSMcLSiuBO8PBCk-jDYX2fu8U1wFG8csMRIMUVYbVui7f6CbOKZQpZIYY0rJfMGPUGtVB_DBxdpX70jlkon68QxWrSbN7D-ouoztvY7BOl_zJwWX-wKdYs7JuqcZEZQ7z8md5-TBcxX-9liXJ_Bfk5Hf7YjQxA</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Wang, Dawei</creator><creator>Cheng, Zhuoxin</creator><creator>Zhao, Ming</creator><creator>Jiao, Chengbin</creator><creator>Meng, Qinghui</creator><creator>Pan, Huayang</creator><creator>Xie, Yu</creator><creator>Li, Long</creator><creator>Zhu, Yexing</creator><creator>Wang, Wei</creator><creator>Qu, Chunlei</creator><creator>Liang, Deshen</creator><general>Dove Medical Press Limited</general><general>Taylor & Francis Ltd</general><general>Dove Medical Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</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>K9.</scope><scope>M0S</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20190101</creationdate><title>PTPN9 induces cell apoptosis by mitigating the activation of Stat3 and acts as a tumor suppressor in colorectal cancer</title><author>Wang, Dawei ; 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Here, we aimed to identify the roles of protein tyrosine phosphatase nonreceptor type 9 (PTPN9), a cytoplasmic PTP, in the development of colorectal cancer and elucidate the regulatory mechanism involved.
Cell viability assessment, colony formation assay, caspase-3 and caspase-9 activity assay, real-time PCR, and Western blot analysis were applied.
Our results showed that PTPN9 expression was frequently downregulated in colorectal cancer tissues compared with adjacent normal tissues. Overexpression of PTPN9 mitigated cell growth and colony formation and induced cell apoptosis in colorectal cancer. Conversely, PTPN9 knockdown promoted cell growth and survival. Moreover, PTPN9 negatively regulated the activation of Stat3 and depressed its nuclear translocation in colorectal cancer. The effects of PTPN9 knockdown on cell apoptosis were attenuated by inhibition of the Stat3 pathway.
These results indicate that PTPN9 inhibits cell growth and survival by repressing the activation of Stat3 in colorectal cancer, which suggests an important underlying mechanism of regulating cell growth and provides a novel candidate therapeutic target for colorectal cancer.</abstract><cop>New Zealand</cop><pub>Dove Medical Press Limited</pub><pmid>30804683</pmid><doi>10.2147/CMAR.S187001</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Apoptosis Breast cancer Cancer therapies Cell cycle Cell growth cell survival Cervical cancer Colorectal cancer Development and progression Gastric cancer Growth factors Health aspects Hospitals Laboratories Liver cancer Metastasis MicroRNAs Original Research Phosphatase Phosphatases Proteins PTPMeg2 PTPN9 Scientific equipment and supplies industry Stat3 Surgery Tumors Tyrosine |
title | PTPN9 induces cell apoptosis by mitigating the activation of Stat3 and acts as a tumor suppressor in colorectal cancer |
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