New Insight on Solute Carrier Family 27 Member 6 (SLC27A6) in Tumoral and Non-Tumoral Breast Cells
Long-chain fatty acids are the most abundant fatty acids and are essential for various physiological processes. Translocation of long-chain fatty acids across cell membrane is dependent on transport proteins. Solute carrier family 27 member 6 (SLC27A6) is a transport protein which mediates long-chai...
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Veröffentlicht in: | International journal of medical sciences 2019-01, Vol.16 (3), p.366-375 |
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description | Long-chain fatty acids are the most abundant fatty acids and are essential for various physiological processes. Translocation of long-chain fatty acids across cell membrane is dependent on transport proteins. Solute carrier family 27 member 6 (SLC27A6) is a transport protein which mediates long-chain fatty acid uptake. The bioinformatic analysis revealed that the expression of SLC27A6 in non-tumoral breast tissue was higher than that in tumoral breast cancer in clinic samples. When SLC27A6 expression in non-tumorigenic cell H184B5F5/M10 was repressed, the fatty acids uptake capacity and cell proliferation was inhibited, and cell cycle was delayed. The protein expression of cell cycle regulators including cell division protein kinase 4 (CDK4), CDK6, and cyclin D1 was significantly decreased in SLC27A6-silenced H184B5F5/M10. By contrast, relatively low SLC27A6 expression in tumorigenic breast cancer cell Hs578T when compared to H184B5F5/M10. Repressing SLC27A6 expression did not affect these phenotypes in Hs578T. The interaction network of SLC27A6 was further investigated via STRING database. The function of these SLC27A6-associated proteins mainly involved in lipid biosynthesis, fatty acid metabolic process, and fatty acid transport. In conclusion, this study reveals inverse correlation between SLC27A6 expression and tumoral tissues and provides a new insight into SLC27A6-mediated cell growth and cell cycle regulation in non-tumorigenic breast cells. |
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Translocation of long-chain fatty acids across cell membrane is dependent on transport proteins. Solute carrier family 27 member 6 (SLC27A6) is a transport protein which mediates long-chain fatty acid uptake. The bioinformatic analysis revealed that the expression of SLC27A6 in non-tumoral breast tissue was higher than that in tumoral breast cancer in clinic samples. When SLC27A6 expression in non-tumorigenic cell H184B5F5/M10 was repressed, the fatty acids uptake capacity and cell proliferation was inhibited, and cell cycle was delayed. The protein expression of cell cycle regulators including cell division protein kinase 4 (CDK4), CDK6, and cyclin D1 was significantly decreased in SLC27A6-silenced H184B5F5/M10. By contrast, relatively low SLC27A6 expression in tumorigenic breast cancer cell Hs578T when compared to H184B5F5/M10. Repressing SLC27A6 expression did not affect these phenotypes in Hs578T. The interaction network of SLC27A6 was further investigated via STRING database. The function of these SLC27A6-associated proteins mainly involved in lipid biosynthesis, fatty acid metabolic process, and fatty acid transport. In conclusion, this study reveals inverse correlation between SLC27A6 expression and tumoral tissues and provides a new insight into SLC27A6-mediated cell growth and cell cycle regulation in non-tumorigenic breast cells.</description><identifier>ISSN: 1449-1907</identifier><identifier>EISSN: 1449-1907</identifier><identifier>DOI: 10.7150/ijms.29946</identifier><identifier>PMID: 30911270</identifier><language>eng</language><publisher>Australia: Ivyspring International Publisher</publisher><subject>Research Paper</subject><ispartof>International journal of medical sciences, 2019-01, Vol.16 (3), p.366-375</ispartof><rights>Ivyspring International Publisher 2019</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c378t-116e127a982af1dca76563ad96e7c5c6d73bb0a86401aefe5e498819d550c68d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6428986/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6428986/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30911270$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yen, Meng-Chi</creatorcontrib><creatorcontrib>Chou, Shih-Kai</creatorcontrib><creatorcontrib>Kan, Jung-Yu</creatorcontrib><creatorcontrib>Kuo, Po-Lin</creatorcontrib><creatorcontrib>Hou, Ming-Feng</creatorcontrib><creatorcontrib>Hsu, Ya-Ling</creatorcontrib><title>New Insight on Solute Carrier Family 27 Member 6 (SLC27A6) in Tumoral and Non-Tumoral Breast Cells</title><title>International journal of medical sciences</title><addtitle>Int J Med Sci</addtitle><description>Long-chain fatty acids are the most abundant fatty acids and are essential for various physiological processes. Translocation of long-chain fatty acids across cell membrane is dependent on transport proteins. Solute carrier family 27 member 6 (SLC27A6) is a transport protein which mediates long-chain fatty acid uptake. The bioinformatic analysis revealed that the expression of SLC27A6 in non-tumoral breast tissue was higher than that in tumoral breast cancer in clinic samples. When SLC27A6 expression in non-tumorigenic cell H184B5F5/M10 was repressed, the fatty acids uptake capacity and cell proliferation was inhibited, and cell cycle was delayed. The protein expression of cell cycle regulators including cell division protein kinase 4 (CDK4), CDK6, and cyclin D1 was significantly decreased in SLC27A6-silenced H184B5F5/M10. By contrast, relatively low SLC27A6 expression in tumorigenic breast cancer cell Hs578T when compared to H184B5F5/M10. Repressing SLC27A6 expression did not affect these phenotypes in Hs578T. The interaction network of SLC27A6 was further investigated via STRING database. The function of these SLC27A6-associated proteins mainly involved in lipid biosynthesis, fatty acid metabolic process, and fatty acid transport. In conclusion, this study reveals inverse correlation between SLC27A6 expression and tumoral tissues and provides a new insight into SLC27A6-mediated cell growth and cell cycle regulation in non-tumorigenic breast cells.</description><subject>Research Paper</subject><issn>1449-1907</issn><issn>1449-1907</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpVkctOwzAQRS0EoqWw4QOQlwUpxc7Djw1SiXhUKrAA1paTTFpXSVzsBNS_J0BBZTUznqs71zoInVIy4TQhl2ZV-0koZcz20JDGsQyoJHx_px-gI-9XhERhxOkhGkREUhpyMkTZI3zgWePNYtli2-BnW3Ut4FQ7Z8DhW12baoNDjh-gzvoHhsfP8zTkU3aOTYNfuto6XWHdFPjRNsHvfO1A-xanUFX-GB2UuvJwsq0j9Hp785LeB_Onu1k6nQd5xEUbUMqgz6SlCHVJi1xzlrBIF5IBz5OcFTzKMqIFiwnVUEICsRSCyiJJSM5EEY3Q1Y_vustqKHJo2j6KWjtTa7dRVhv1f9OYpVrYd8XiUEjBeoPx1sDZtw58q2rj8_4LugHbeRVSyYWUNJG99OJHmjvrvYPy7wwl6guK-oKivqH04rPdYH_SXwrRJ1c9hu0</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Yen, Meng-Chi</creator><creator>Chou, Shih-Kai</creator><creator>Kan, Jung-Yu</creator><creator>Kuo, Po-Lin</creator><creator>Hou, Ming-Feng</creator><creator>Hsu, Ya-Ling</creator><general>Ivyspring International Publisher</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190101</creationdate><title>New Insight on Solute Carrier Family 27 Member 6 (SLC27A6) in Tumoral and Non-Tumoral Breast Cells</title><author>Yen, Meng-Chi ; Chou, Shih-Kai ; Kan, Jung-Yu ; Kuo, Po-Lin ; Hou, Ming-Feng ; Hsu, Ya-Ling</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c378t-116e127a982af1dca76563ad96e7c5c6d73bb0a86401aefe5e498819d550c68d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Research Paper</topic><toplevel>online_resources</toplevel><creatorcontrib>Yen, Meng-Chi</creatorcontrib><creatorcontrib>Chou, Shih-Kai</creatorcontrib><creatorcontrib>Kan, Jung-Yu</creatorcontrib><creatorcontrib>Kuo, Po-Lin</creatorcontrib><creatorcontrib>Hou, Ming-Feng</creatorcontrib><creatorcontrib>Hsu, Ya-Ling</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of medical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yen, Meng-Chi</au><au>Chou, Shih-Kai</au><au>Kan, Jung-Yu</au><au>Kuo, Po-Lin</au><au>Hou, Ming-Feng</au><au>Hsu, Ya-Ling</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New Insight on Solute Carrier Family 27 Member 6 (SLC27A6) in Tumoral and Non-Tumoral Breast Cells</atitle><jtitle>International journal of medical sciences</jtitle><addtitle>Int J Med Sci</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>16</volume><issue>3</issue><spage>366</spage><epage>375</epage><pages>366-375</pages><issn>1449-1907</issn><eissn>1449-1907</eissn><abstract>Long-chain fatty acids are the most abundant fatty acids and are essential for various physiological processes. Translocation of long-chain fatty acids across cell membrane is dependent on transport proteins. Solute carrier family 27 member 6 (SLC27A6) is a transport protein which mediates long-chain fatty acid uptake. The bioinformatic analysis revealed that the expression of SLC27A6 in non-tumoral breast tissue was higher than that in tumoral breast cancer in clinic samples. When SLC27A6 expression in non-tumorigenic cell H184B5F5/M10 was repressed, the fatty acids uptake capacity and cell proliferation was inhibited, and cell cycle was delayed. The protein expression of cell cycle regulators including cell division protein kinase 4 (CDK4), CDK6, and cyclin D1 was significantly decreased in SLC27A6-silenced H184B5F5/M10. By contrast, relatively low SLC27A6 expression in tumorigenic breast cancer cell Hs578T when compared to H184B5F5/M10. Repressing SLC27A6 expression did not affect these phenotypes in Hs578T. The interaction network of SLC27A6 was further investigated via STRING database. The function of these SLC27A6-associated proteins mainly involved in lipid biosynthesis, fatty acid metabolic process, and fatty acid transport. In conclusion, this study reveals inverse correlation between SLC27A6 expression and tumoral tissues and provides a new insight into SLC27A6-mediated cell growth and cell cycle regulation in non-tumorigenic breast cells.</abstract><cop>Australia</cop><pub>Ivyspring International Publisher</pub><pmid>30911270</pmid><doi>10.7150/ijms.29946</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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title | New Insight on Solute Carrier Family 27 Member 6 (SLC27A6) in Tumoral and Non-Tumoral Breast Cells |
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