High aldehyde dehydrogenase activity enhances stem cell features in breast cancer cells by activating hypoxia-inducible factor-2[alpha]
High aldehyde dehydrogenase (ALDH) activity has been recognized as a marker of cancer stem cells (CSCs) in breast cancer. In this study, we examined whether inhibition of ALDH activity suppresses stem-like cell properties in a 4T1 syngeneic mouse model of breast cancer. We found that ALDH-positive 4...
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Veröffentlicht in: | Cancer letters 2013-06, Vol.333 (1), p.18 |
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creator | Kim, Ran-Ju Park, Jeong-Ran Roh, Kyung-Jin Choi, A-Ram Kim, Soo-Rim Kim, Pyeung-Hyeun Yu, Jong Han Lee, Jong Won Ahn, Sei-Hyun Gong, Gyungyub Hwang, Jae-Woong Kang, Kyung-Sun Kong, Gu Sheen, Yhun Yhong Nam, Jeong-Seok |
description | High aldehyde dehydrogenase (ALDH) activity has been recognized as a marker of cancer stem cells (CSCs) in breast cancer. In this study, we examined whether inhibition of ALDH activity suppresses stem-like cell properties in a 4T1 syngeneic mouse model of breast cancer. We found that ALDH-positive 4T1 cells showed stem cell-like propertiesin vitroandin vivo. Blockade of ALDH activity reduced the growth of CSCs in breast cancer cell lines. Treatment of mice with the ALDH inhibitor diethylaminobenzaldehyde (DEAB) significantly suppressed 4T1 cell metastasis to the lung. Recent evidence suggests that ALDH affects the response of stem cells to hypoxia; therefore, we examined a possible link between ALDH and hypoxia signaling in breast cancer. Hypoxia-inducible factor-2α (HIF-2α) was highly dysregulated in ALDH-positive 4T1 cells. We observed that ALDH was highly correlated with the HIF-2α expression in breast cancer cell lines and tissues. DEAB treatment of breast cancer cells reduced the expression of HIF-2αin vitro. In addition, reduction of HIF-2α expression suppressedin vitroself-renewal ability andin vivotumor initiation in ALDH-positive 4T1 cells. Therefore, our findings may provide the evidence necessary for exploring a new strategy in the treatment of breast cancer. |
doi_str_mv | 10.1016/j.canlet.2012.11.026 |
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In this study, we examined whether inhibition of ALDH activity suppresses stem-like cell properties in a 4T1 syngeneic mouse model of breast cancer. We found that ALDH-positive 4T1 cells showed stem cell-like propertiesin vitroandin vivo. Blockade of ALDH activity reduced the growth of CSCs in breast cancer cell lines. Treatment of mice with the ALDH inhibitor diethylaminobenzaldehyde (DEAB) significantly suppressed 4T1 cell metastasis to the lung. Recent evidence suggests that ALDH affects the response of stem cells to hypoxia; therefore, we examined a possible link between ALDH and hypoxia signaling in breast cancer. Hypoxia-inducible factor-2α (HIF-2α) was highly dysregulated in ALDH-positive 4T1 cells. We observed that ALDH was highly correlated with the HIF-2α expression in breast cancer cell lines and tissues. DEAB treatment of breast cancer cells reduced the expression of HIF-2αin vitro. In addition, reduction of HIF-2α expression suppressedin vitroself-renewal ability andin vivotumor initiation in ALDH-positive 4T1 cells. Therefore, our findings may provide the evidence necessary for exploring a new strategy in the treatment of breast cancer.</description><identifier>ISSN: 0304-3835</identifier><identifier>EISSN: 1872-7980</identifier><identifier>DOI: 10.1016/j.canlet.2012.11.026</identifier><language>eng</language><publisher>Clare: Elsevier Limited</publisher><subject>Breast cancer ; Cancer therapies ; Confidence intervals ; Dehydrogenases ; Hypoxia ; Metabolism ; Metastasis ; Mortality ; Motility ; Population ; Software ; Stem cells ; Studies ; Tumors</subject><ispartof>Cancer letters, 2013-06, Vol.333 (1), p.18</ispartof><rights>Copyright Elsevier Limited Jun 1, 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Kim, Ran-Ju</creatorcontrib><creatorcontrib>Park, Jeong-Ran</creatorcontrib><creatorcontrib>Roh, Kyung-Jin</creatorcontrib><creatorcontrib>Choi, A-Ram</creatorcontrib><creatorcontrib>Kim, Soo-Rim</creatorcontrib><creatorcontrib>Kim, Pyeung-Hyeun</creatorcontrib><creatorcontrib>Yu, Jong Han</creatorcontrib><creatorcontrib>Lee, Jong Won</creatorcontrib><creatorcontrib>Ahn, Sei-Hyun</creatorcontrib><creatorcontrib>Gong, Gyungyub</creatorcontrib><creatorcontrib>Hwang, Jae-Woong</creatorcontrib><creatorcontrib>Kang, Kyung-Sun</creatorcontrib><creatorcontrib>Kong, Gu</creatorcontrib><creatorcontrib>Sheen, Yhun Yhong</creatorcontrib><creatorcontrib>Nam, Jeong-Seok</creatorcontrib><title>High aldehyde dehydrogenase activity enhances stem cell features in breast cancer cells by activating hypoxia-inducible factor-2[alpha]</title><title>Cancer letters</title><description>High aldehyde dehydrogenase (ALDH) activity has been recognized as a marker of cancer stem cells (CSCs) in breast cancer. In this study, we examined whether inhibition of ALDH activity suppresses stem-like cell properties in a 4T1 syngeneic mouse model of breast cancer. We found that ALDH-positive 4T1 cells showed stem cell-like propertiesin vitroandin vivo. Blockade of ALDH activity reduced the growth of CSCs in breast cancer cell lines. Treatment of mice with the ALDH inhibitor diethylaminobenzaldehyde (DEAB) significantly suppressed 4T1 cell metastasis to the lung. Recent evidence suggests that ALDH affects the response of stem cells to hypoxia; therefore, we examined a possible link between ALDH and hypoxia signaling in breast cancer. Hypoxia-inducible factor-2α (HIF-2α) was highly dysregulated in ALDH-positive 4T1 cells. We observed that ALDH was highly correlated with the HIF-2α expression in breast cancer cell lines and tissues. DEAB treatment of breast cancer cells reduced the expression of HIF-2αin vitro. In addition, reduction of HIF-2α expression suppressedin vitroself-renewal ability andin vivotumor initiation in ALDH-positive 4T1 cells. Therefore, our findings may provide the evidence necessary for exploring a new strategy in the treatment of breast cancer.</description><subject>Breast cancer</subject><subject>Cancer therapies</subject><subject>Confidence intervals</subject><subject>Dehydrogenases</subject><subject>Hypoxia</subject><subject>Metabolism</subject><subject>Metastasis</subject><subject>Mortality</subject><subject>Motility</subject><subject>Population</subject><subject>Software</subject><subject>Stem cells</subject><subject>Studies</subject><subject>Tumors</subject><issn>0304-3835</issn><issn>1872-7980</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqNj01OhTAUhRujiahvBw5u4hhsy09xbDRvAc6MebmUC5T0FWyLkRW4bfHpAhyd5HzfGRzGbgXPBBfV_ZhpdJZiJrmQmRAZl9UZS0StZKoean7OEp7zIs3rvLxkVyGMnPOyUGXCvvamHwBtS8PaEpzCTz05DASoo_kwcQVyAzpNAUKkI2iyFjrCuPitMg4aTxgi6B_Hn3CAZv2dYzSuh2Gdp0-DqXHtok1jCbqNTj6Vr2jnAd9u2EWHNtDuL6_Z3fPTy-M-nf30vlCIh3FavNvQQVRFuf2slMr_Z30DGi9cXw</recordid><startdate>20130601</startdate><enddate>20130601</enddate><creator>Kim, Ran-Ju</creator><creator>Park, Jeong-Ran</creator><creator>Roh, Kyung-Jin</creator><creator>Choi, A-Ram</creator><creator>Kim, Soo-Rim</creator><creator>Kim, Pyeung-Hyeun</creator><creator>Yu, Jong Han</creator><creator>Lee, Jong Won</creator><creator>Ahn, Sei-Hyun</creator><creator>Gong, Gyungyub</creator><creator>Hwang, Jae-Woong</creator><creator>Kang, Kyung-Sun</creator><creator>Kong, Gu</creator><creator>Sheen, Yhun Yhong</creator><creator>Nam, Jeong-Seok</creator><general>Elsevier Limited</general><scope>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope></search><sort><creationdate>20130601</creationdate><title>High aldehyde dehydrogenase activity enhances stem cell features in breast cancer cells by activating hypoxia-inducible factor-2[alpha]</title><author>Kim, Ran-Ju ; Park, Jeong-Ran ; Roh, Kyung-Jin ; Choi, A-Ram ; Kim, Soo-Rim ; Kim, Pyeung-Hyeun ; Yu, Jong Han ; Lee, Jong Won ; Ahn, Sei-Hyun ; Gong, Gyungyub ; Hwang, Jae-Woong ; Kang, Kyung-Sun ; Kong, Gu ; Sheen, Yhun Yhong ; Nam, Jeong-Seok</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_16450126773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Breast cancer</topic><topic>Cancer therapies</topic><topic>Confidence intervals</topic><topic>Dehydrogenases</topic><topic>Hypoxia</topic><topic>Metabolism</topic><topic>Metastasis</topic><topic>Mortality</topic><topic>Motility</topic><topic>Population</topic><topic>Software</topic><topic>Stem cells</topic><topic>Studies</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Ran-Ju</creatorcontrib><creatorcontrib>Park, Jeong-Ran</creatorcontrib><creatorcontrib>Roh, Kyung-Jin</creatorcontrib><creatorcontrib>Choi, A-Ram</creatorcontrib><creatorcontrib>Kim, Soo-Rim</creatorcontrib><creatorcontrib>Kim, Pyeung-Hyeun</creatorcontrib><creatorcontrib>Yu, Jong Han</creatorcontrib><creatorcontrib>Lee, Jong Won</creatorcontrib><creatorcontrib>Ahn, Sei-Hyun</creatorcontrib><creatorcontrib>Gong, Gyungyub</creatorcontrib><creatorcontrib>Hwang, Jae-Woong</creatorcontrib><creatorcontrib>Kang, Kyung-Sun</creatorcontrib><creatorcontrib>Kong, Gu</creatorcontrib><creatorcontrib>Sheen, Yhun Yhong</creatorcontrib><creatorcontrib>Nam, Jeong-Seok</creatorcontrib><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><jtitle>Cancer letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Ran-Ju</au><au>Park, Jeong-Ran</au><au>Roh, Kyung-Jin</au><au>Choi, A-Ram</au><au>Kim, Soo-Rim</au><au>Kim, Pyeung-Hyeun</au><au>Yu, Jong Han</au><au>Lee, Jong Won</au><au>Ahn, Sei-Hyun</au><au>Gong, Gyungyub</au><au>Hwang, Jae-Woong</au><au>Kang, Kyung-Sun</au><au>Kong, Gu</au><au>Sheen, Yhun Yhong</au><au>Nam, Jeong-Seok</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High aldehyde dehydrogenase activity enhances stem cell features in breast cancer cells by activating hypoxia-inducible factor-2[alpha]</atitle><jtitle>Cancer letters</jtitle><date>2013-06-01</date><risdate>2013</risdate><volume>333</volume><issue>1</issue><spage>18</spage><pages>18-</pages><issn>0304-3835</issn><eissn>1872-7980</eissn><abstract>High aldehyde dehydrogenase (ALDH) activity has been recognized as a marker of cancer stem cells (CSCs) in breast cancer. In this study, we examined whether inhibition of ALDH activity suppresses stem-like cell properties in a 4T1 syngeneic mouse model of breast cancer. We found that ALDH-positive 4T1 cells showed stem cell-like propertiesin vitroandin vivo. Blockade of ALDH activity reduced the growth of CSCs in breast cancer cell lines. Treatment of mice with the ALDH inhibitor diethylaminobenzaldehyde (DEAB) significantly suppressed 4T1 cell metastasis to the lung. Recent evidence suggests that ALDH affects the response of stem cells to hypoxia; therefore, we examined a possible link between ALDH and hypoxia signaling in breast cancer. Hypoxia-inducible factor-2α (HIF-2α) was highly dysregulated in ALDH-positive 4T1 cells. We observed that ALDH was highly correlated with the HIF-2α expression in breast cancer cell lines and tissues. DEAB treatment of breast cancer cells reduced the expression of HIF-2αin vitro. In addition, reduction of HIF-2α expression suppressedin vitroself-renewal ability andin vivotumor initiation in ALDH-positive 4T1 cells. Therefore, our findings may provide the evidence necessary for exploring a new strategy in the treatment of breast cancer.</abstract><cop>Clare</cop><pub>Elsevier Limited</pub><doi>10.1016/j.canlet.2012.11.026</doi></addata></record> |
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subjects | Breast cancer Cancer therapies Confidence intervals Dehydrogenases Hypoxia Metabolism Metastasis Mortality Motility Population Software Stem cells Studies Tumors |
title | High aldehyde dehydrogenase activity enhances stem cell features in breast cancer cells by activating hypoxia-inducible factor-2[alpha] |
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