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Phosphorylation and activation of STAT proteins by hypoxia in breast cancer cells
Several constitutively activated signal transducers and activators of transcription (STAT) proteins have been observed in a wide number of human cancer cell lines and primary tumors. Normal cells maintain normoxic conditions but tumor cells are characteristically hypoxic. We studied the altered acti...
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Published in: | Breast (Edinburgh) 2006-04, Vol.15 (2), p.187-195 |
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container_title | Breast (Edinburgh) |
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creator | Lee, Moon Young Joung, Youn Hee Lim, Eun Joung Park, Jong-Hwan Ye, Sang-Kyu Park, Taekyu Zhang, Zheng Park, Dong Ki Lee, Kwang Jeon Yang, Young Mok |
description | Several constitutively activated signal transducers and activators of transcription (STAT) proteins have been observed in a wide number of human cancer cell lines and primary tumors. Normal cells maintain normoxic conditions but tumor cells are characteristically hypoxic. We studied the altered activation and tyrosine phosphorylation of STATs under hypoxic conditions (2% O
2) or desferrioxamine (DFO) treatment in mouse mammary epithelial cells (HC11) and a human breast cancer cell line (MCF-7). STAT1, -3 and -5 proteins are especially important and are observed at elevated levels in tumorigenesis. We also investigated the serine phosphorylation of STAT1, -3, and -5 under hypoxic conditions or DFO treatment in HC11 and MCF-7 cells. Here we show that DFO or hypoxia stimulates the tyrosine and/or serine phosphorylation and the expression of STAT proteins in breast cancer cells. Our data suggest that DFO or hypoxic condition is a critical stimulator for the activation of STAT proteins in breast cancer cells. These results may provide the basis for identifying another mechanism of breast tumorigenesis via the JAK/STAT pathway in hypoxia. Also, activation of STAT proteins by hypoxia may play an important role in the physiological phenomenon of embryonic stem cells and old cells with hypoxic conditions. |
doi_str_mv | 10.1016/j.breast.2005.05.005 |
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2) or desferrioxamine (DFO) treatment in mouse mammary epithelial cells (HC11) and a human breast cancer cell line (MCF-7). STAT1, -3 and -5 proteins are especially important and are observed at elevated levels in tumorigenesis. We also investigated the serine phosphorylation of STAT1, -3, and -5 under hypoxic conditions or DFO treatment in HC11 and MCF-7 cells. Here we show that DFO or hypoxia stimulates the tyrosine and/or serine phosphorylation and the expression of STAT proteins in breast cancer cells. Our data suggest that DFO or hypoxic condition is a critical stimulator for the activation of STAT proteins in breast cancer cells. These results may provide the basis for identifying another mechanism of breast tumorigenesis via the JAK/STAT pathway in hypoxia. Also, activation of STAT proteins by hypoxia may play an important role in the physiological phenomenon of embryonic stem cells and old cells with hypoxic conditions.</description><identifier>ISSN: 0960-9776</identifier><identifier>EISSN: 1532-3080</identifier><identifier>DOI: 10.1016/j.breast.2005.05.005</identifier><identifier>PMID: 16084091</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Animals ; Breast cancer cell ; Breast Neoplasms - metabolism ; Cell Hypoxia ; Cell Line, Tumor - drug effects ; Cell Line, Tumor - metabolism ; Deferoxamine - pharmacology ; Female ; Humans ; Hypoxia ; Mammary Glands, Animal - metabolism ; Mice ; Phosphorylation - drug effects ; Serine phosphorylation ; STAT ; STAT Transcription Factors - metabolism ; STAT1 Transcription Factor - metabolism ; STAT3 Transcription Factor - metabolism ; STAT5 Transcription Factor - metabolism ; Tyrosine phosphorylation</subject><ispartof>Breast (Edinburgh), 2006-04, Vol.15 (2), p.187-195</ispartof><rights>2005 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c426t-b26c7a429d0e03546ea1431d87c6c51051c81b8301e0178f248befefc2fdf3bd3</citedby><cites>FETCH-LOGICAL-c426t-b26c7a429d0e03546ea1431d87c6c51051c81b8301e0178f248befefc2fdf3bd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16084091$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Moon Young</creatorcontrib><creatorcontrib>Joung, Youn Hee</creatorcontrib><creatorcontrib>Lim, Eun Joung</creatorcontrib><creatorcontrib>Park, Jong-Hwan</creatorcontrib><creatorcontrib>Ye, Sang-Kyu</creatorcontrib><creatorcontrib>Park, Taekyu</creatorcontrib><creatorcontrib>Zhang, Zheng</creatorcontrib><creatorcontrib>Park, Dong Ki</creatorcontrib><creatorcontrib>Lee, Kwang Jeon</creatorcontrib><creatorcontrib>Yang, Young Mok</creatorcontrib><title>Phosphorylation and activation of STAT proteins by hypoxia in breast cancer cells</title><title>Breast (Edinburgh)</title><addtitle>Breast</addtitle><description>Several constitutively activated signal transducers and activators of transcription (STAT) proteins have been observed in a wide number of human cancer cell lines and primary tumors. Normal cells maintain normoxic conditions but tumor cells are characteristically hypoxic. We studied the altered activation and tyrosine phosphorylation of STATs under hypoxic conditions (2% O
2) or desferrioxamine (DFO) treatment in mouse mammary epithelial cells (HC11) and a human breast cancer cell line (MCF-7). STAT1, -3 and -5 proteins are especially important and are observed at elevated levels in tumorigenesis. We also investigated the serine phosphorylation of STAT1, -3, and -5 under hypoxic conditions or DFO treatment in HC11 and MCF-7 cells. Here we show that DFO or hypoxia stimulates the tyrosine and/or serine phosphorylation and the expression of STAT proteins in breast cancer cells. Our data suggest that DFO or hypoxic condition is a critical stimulator for the activation of STAT proteins in breast cancer cells. These results may provide the basis for identifying another mechanism of breast tumorigenesis via the JAK/STAT pathway in hypoxia. Also, activation of STAT proteins by hypoxia may play an important role in the physiological phenomenon of embryonic stem cells and old cells with hypoxic conditions.</description><subject>Animals</subject><subject>Breast cancer cell</subject><subject>Breast Neoplasms - metabolism</subject><subject>Cell Hypoxia</subject><subject>Cell Line, Tumor - drug effects</subject><subject>Cell Line, Tumor - metabolism</subject><subject>Deferoxamine - pharmacology</subject><subject>Female</subject><subject>Humans</subject><subject>Hypoxia</subject><subject>Mammary Glands, Animal - metabolism</subject><subject>Mice</subject><subject>Phosphorylation - drug effects</subject><subject>Serine phosphorylation</subject><subject>STAT</subject><subject>STAT Transcription Factors - metabolism</subject><subject>STAT1 Transcription Factor - metabolism</subject><subject>STAT3 Transcription Factor - metabolism</subject><subject>STAT5 Transcription Factor - metabolism</subject><subject>Tyrosine phosphorylation</subject><issn>0960-9776</issn><issn>1532-3080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNp9UF1LxDAQDKJ45-k_EMmTb62bfqTpi3CIX3Cg4vkc0nTL5eg1Nekd9t_b0gPfhIFlYWZ3Zgi5ZhAyYPxuGxYOle_CCCANR0B6QuYsjaMgBgGnZA45hyDPMj4jF95vASCPuTgnM8ZBJJCzOfl431jfbqzra9UZ21DVlFTpzhym1Vb0c71c09bZDk3jadHTTd_aH6OoaehkgWrVaHRUY137S3JWqdrj1XEuyNfT4_rhJVi9Pb8-LFeBTiLeBUXEdaaSKC8BIU4TjoolMStFprlOGaRMC1aIGBgCy0QVJaLACisdVWUVF2W8ILfT3cHa9x59J3fGjw5Ug3bvJc_yASIaiMlE1M5677CSrTM75XrJQI5Vyq2ccsixSjkC0kF2c7y_L3ZY_omO3Q2E-4mAQ8qDQSe9NjgUURqHupOlNf9_-AUAtodQ</recordid><startdate>20060401</startdate><enddate>20060401</enddate><creator>Lee, Moon Young</creator><creator>Joung, Youn Hee</creator><creator>Lim, Eun Joung</creator><creator>Park, Jong-Hwan</creator><creator>Ye, Sang-Kyu</creator><creator>Park, Taekyu</creator><creator>Zhang, Zheng</creator><creator>Park, Dong Ki</creator><creator>Lee, Kwang Jeon</creator><creator>Yang, Young Mok</creator><general>Elsevier Ltd</general><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>7X8</scope></search><sort><creationdate>20060401</creationdate><title>Phosphorylation and activation of STAT proteins by hypoxia in breast cancer cells</title><author>Lee, Moon Young ; Joung, Youn Hee ; Lim, Eun Joung ; Park, Jong-Hwan ; Ye, Sang-Kyu ; Park, Taekyu ; Zhang, Zheng ; Park, Dong Ki ; Lee, Kwang Jeon ; Yang, Young Mok</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c426t-b26c7a429d0e03546ea1431d87c6c51051c81b8301e0178f248befefc2fdf3bd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Breast cancer cell</topic><topic>Breast Neoplasms - metabolism</topic><topic>Cell Hypoxia</topic><topic>Cell Line, Tumor - drug effects</topic><topic>Cell Line, Tumor - metabolism</topic><topic>Deferoxamine - pharmacology</topic><topic>Female</topic><topic>Humans</topic><topic>Hypoxia</topic><topic>Mammary Glands, Animal - metabolism</topic><topic>Mice</topic><topic>Phosphorylation - drug effects</topic><topic>Serine phosphorylation</topic><topic>STAT</topic><topic>STAT Transcription Factors - metabolism</topic><topic>STAT1 Transcription Factor - metabolism</topic><topic>STAT3 Transcription Factor - metabolism</topic><topic>STAT5 Transcription Factor - metabolism</topic><topic>Tyrosine phosphorylation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Moon Young</creatorcontrib><creatorcontrib>Joung, Youn Hee</creatorcontrib><creatorcontrib>Lim, Eun Joung</creatorcontrib><creatorcontrib>Park, Jong-Hwan</creatorcontrib><creatorcontrib>Ye, Sang-Kyu</creatorcontrib><creatorcontrib>Park, Taekyu</creatorcontrib><creatorcontrib>Zhang, Zheng</creatorcontrib><creatorcontrib>Park, Dong Ki</creatorcontrib><creatorcontrib>Lee, Kwang Jeon</creatorcontrib><creatorcontrib>Yang, Young Mok</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Breast (Edinburgh)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Moon Young</au><au>Joung, Youn Hee</au><au>Lim, Eun Joung</au><au>Park, Jong-Hwan</au><au>Ye, Sang-Kyu</au><au>Park, Taekyu</au><au>Zhang, Zheng</au><au>Park, Dong Ki</au><au>Lee, Kwang Jeon</au><au>Yang, Young Mok</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phosphorylation and activation of STAT proteins by hypoxia in breast cancer cells</atitle><jtitle>Breast (Edinburgh)</jtitle><addtitle>Breast</addtitle><date>2006-04-01</date><risdate>2006</risdate><volume>15</volume><issue>2</issue><spage>187</spage><epage>195</epage><pages>187-195</pages><issn>0960-9776</issn><eissn>1532-3080</eissn><abstract>Several constitutively activated signal transducers and activators of transcription (STAT) proteins have been observed in a wide number of human cancer cell lines and primary tumors. 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2) or desferrioxamine (DFO) treatment in mouse mammary epithelial cells (HC11) and a human breast cancer cell line (MCF-7). STAT1, -3 and -5 proteins are especially important and are observed at elevated levels in tumorigenesis. We also investigated the serine phosphorylation of STAT1, -3, and -5 under hypoxic conditions or DFO treatment in HC11 and MCF-7 cells. Here we show that DFO or hypoxia stimulates the tyrosine and/or serine phosphorylation and the expression of STAT proteins in breast cancer cells. Our data suggest that DFO or hypoxic condition is a critical stimulator for the activation of STAT proteins in breast cancer cells. These results may provide the basis for identifying another mechanism of breast tumorigenesis via the JAK/STAT pathway in hypoxia. Also, activation of STAT proteins by hypoxia may play an important role in the physiological phenomenon of embryonic stem cells and old cells with hypoxic conditions.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>16084091</pmid><doi>10.1016/j.breast.2005.05.005</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Breast cancer cell Breast Neoplasms - metabolism Cell Hypoxia Cell Line, Tumor - drug effects Cell Line, Tumor - metabolism Deferoxamine - pharmacology Female Humans Hypoxia Mammary Glands, Animal - metabolism Mice Phosphorylation - drug effects Serine phosphorylation STAT STAT Transcription Factors - metabolism STAT1 Transcription Factor - metabolism STAT3 Transcription Factor - metabolism STAT5 Transcription Factor - metabolism Tyrosine phosphorylation |
title | Phosphorylation and activation of STAT proteins by hypoxia in breast cancer cells |
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