The developmental transcription factor IRF6 attenuates ABCG2 gene expression and distinctively reverses stemness phenotype in nasopharyngeal carcinoma
Nasopharyngeal carcinoma (NPC), which originates from the nasopharynx, is highly prevalent in Southern China and Southeast Asia, and more than 90% of all NPCs are non-keratinizing undifferentiated cells or poorly differentiated squamous cells. Cancer stem cells (CSCs) are capable of self-renewal and...
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Veröffentlicht in: | Cancer letters 2018-09, Vol.431, p.230-243 |
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creator | Xu, Liang Huang, Tie-Jun Hu, Hao Wang, Meng-Yao Shi, Si-Mei Yang, Qin Lin, Fen Qiang, Yuan-Yuan Mei, Yan Lang, Yan-Hong Li, Chang-Zhi Peng, Li-Xia Zheng, Li-Sheng Huang, Jia-Ling Li, Xin-Jian Zhang, Shi-Jun Qian, Chao-Nan Huang, Bi-Jun |
description | Nasopharyngeal carcinoma (NPC), which originates from the nasopharynx, is highly prevalent in Southern China and Southeast Asia, and more than 90% of all NPCs are non-keratinizing undifferentiated cells or poorly differentiated squamous cells. Cancer stem cells (CSCs) are capable of self-renewal and have differentiation potential. These properties form the basis of cancer initiation, development, and radiochemoresistance. However, the molecular mechanisms underlying NPC CSC maintenance remain poorly understood. Here, genomic expression profiling using our previously established monoclonal cellular and animal models revealed that interferon regulatory factor 6 (IRF6) was downregulated in highly metastatic NPC cells, cancer stem-like NPC cells and animal models. Functional assays revealed that elevated IRF6 expression suppressed cell proliferation, growth, CSCs properties and enhanced cell chemotherapeutic sensitivity. However, silencing IRF6 resulted in opposing effects. Moreover, we determined that as a tumor suppressor gene and transcription factor, IRF6 directly bound the upstream region of the ATP-binding cassette sub-family G member 2 (ABCG2) DNA element and suppressed target ABCG2 expression in NPC cells. Consistently, an inverse correlation was observed between the mRNA levels of IRF6 and ABCG2 in clinical NPC samples. With these results, we provide the first evidence that IRF6 directly targets the ABCG2 gene and selectively kills CSCs in NPC and that IRF6 may be a valuable tool for developing new CSC-targeted treatment strategies for undifferentiated NPC patients.
•IRF6 is initially found to be down regulated in our well established high-metastasis NPC cellular clone, and further series functional studies confirmed that IRF6 can inhibit the growth, migration, invasion, and metastasis of NPC cells.•Elevated IRF6 expression can enhance NPC chemotherapeutic sensitivity.•IRF6 down-regulates the expression of ABCG2 in NPC.•IRF6 can selectively kill nasopharyngeal carcinoma stem cells and overexpression of IRF6 is a promising approach for anti-stem cell targeted therapy. |
doi_str_mv | 10.1016/j.canlet.2017.10.016 |
format | Article |
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•IRF6 is initially found to be down regulated in our well established high-metastasis NPC cellular clone, and further series functional studies confirmed that IRF6 can inhibit the growth, migration, invasion, and metastasis of NPC cells.•Elevated IRF6 expression can enhance NPC chemotherapeutic sensitivity.•IRF6 down-regulates the expression of ABCG2 in NPC.•IRF6 can selectively kill nasopharyngeal carcinoma stem cells and overexpression of IRF6 is a promising approach for anti-stem cell targeted therapy.</description><identifier>ISSN: 0304-3835</identifier><identifier>EISSN: 1872-7980</identifier><identifier>DOI: 10.1016/j.canlet.2017.10.016</identifier><identifier>PMID: 29111349</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>ABCG2 ; ABCG2 gene ; Animal models ; Cancer stem cells ; Cancer therapies ; Cell growth ; Cell proliferation ; Cell self-renewal ; Chemotherapy ; Deoxyribonucleic acid ; DNA ; Gene expression ; Grants ; Interferon ; Interferon regulatory factor ; IRF6 ; Metastases ; Metastasis ; Molecular modelling ; Mutation ; Nasopharyngeal carcinoma ; Nasopharynx ; Phenotypes ; Radiation therapy ; Squamous cells ; Stem cell transplantation ; Stem cells ; Throat cancer ; Transcription ; Transcription factors ; Tumor suppressor genes ; Tumorigenesis</subject><ispartof>Cancer letters, 2018-09, Vol.431, p.230-243</ispartof><rights>2017 Elsevier B.V.</rights><rights>Copyright © 2017 Elsevier B.V. All rights reserved.</rights><rights>2017. Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c305t-8df6039312d9b46158c869cecfb27645dd3d59c5a0c5b4efe2cbd3c83651e2823</citedby><cites>FETCH-LOGICAL-c305t-8df6039312d9b46158c869cecfb27645dd3d59c5a0c5b4efe2cbd3c83651e2823</cites><orcidid>0000-0002-4292-1006</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0304383517306511$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29111349$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xu, Liang</creatorcontrib><creatorcontrib>Huang, Tie-Jun</creatorcontrib><creatorcontrib>Hu, Hao</creatorcontrib><creatorcontrib>Wang, Meng-Yao</creatorcontrib><creatorcontrib>Shi, Si-Mei</creatorcontrib><creatorcontrib>Yang, Qin</creatorcontrib><creatorcontrib>Lin, Fen</creatorcontrib><creatorcontrib>Qiang, Yuan-Yuan</creatorcontrib><creatorcontrib>Mei, Yan</creatorcontrib><creatorcontrib>Lang, Yan-Hong</creatorcontrib><creatorcontrib>Li, Chang-Zhi</creatorcontrib><creatorcontrib>Peng, Li-Xia</creatorcontrib><creatorcontrib>Zheng, Li-Sheng</creatorcontrib><creatorcontrib>Huang, Jia-Ling</creatorcontrib><creatorcontrib>Li, Xin-Jian</creatorcontrib><creatorcontrib>Zhang, Shi-Jun</creatorcontrib><creatorcontrib>Qian, Chao-Nan</creatorcontrib><creatorcontrib>Huang, Bi-Jun</creatorcontrib><title>The developmental transcription factor IRF6 attenuates ABCG2 gene expression and distinctively reverses stemness phenotype in nasopharyngeal carcinoma</title><title>Cancer letters</title><addtitle>Cancer Lett</addtitle><description>Nasopharyngeal carcinoma (NPC), which originates from the nasopharynx, is highly prevalent in Southern China and Southeast Asia, and more than 90% of all NPCs are non-keratinizing undifferentiated cells or poorly differentiated squamous cells. Cancer stem cells (CSCs) are capable of self-renewal and have differentiation potential. These properties form the basis of cancer initiation, development, and radiochemoresistance. However, the molecular mechanisms underlying NPC CSC maintenance remain poorly understood. Here, genomic expression profiling using our previously established monoclonal cellular and animal models revealed that interferon regulatory factor 6 (IRF6) was downregulated in highly metastatic NPC cells, cancer stem-like NPC cells and animal models. Functional assays revealed that elevated IRF6 expression suppressed cell proliferation, growth, CSCs properties and enhanced cell chemotherapeutic sensitivity. However, silencing IRF6 resulted in opposing effects. Moreover, we determined that as a tumor suppressor gene and transcription factor, IRF6 directly bound the upstream region of the ATP-binding cassette sub-family G member 2 (ABCG2) DNA element and suppressed target ABCG2 expression in NPC cells. Consistently, an inverse correlation was observed between the mRNA levels of IRF6 and ABCG2 in clinical NPC samples. With these results, we provide the first evidence that IRF6 directly targets the ABCG2 gene and selectively kills CSCs in NPC and that IRF6 may be a valuable tool for developing new CSC-targeted treatment strategies for undifferentiated NPC patients.
•IRF6 is initially found to be down regulated in our well established high-metastasis NPC cellular clone, and further series functional studies confirmed that IRF6 can inhibit the growth, migration, invasion, and metastasis of NPC cells.•Elevated IRF6 expression can enhance NPC chemotherapeutic sensitivity.•IRF6 down-regulates the expression of ABCG2 in NPC.•IRF6 can selectively kill nasopharyngeal carcinoma stem cells and overexpression of IRF6 is a promising approach for anti-stem cell targeted therapy.</description><subject>ABCG2</subject><subject>ABCG2 gene</subject><subject>Animal models</subject><subject>Cancer stem cells</subject><subject>Cancer therapies</subject><subject>Cell growth</subject><subject>Cell proliferation</subject><subject>Cell self-renewal</subject><subject>Chemotherapy</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Gene expression</subject><subject>Grants</subject><subject>Interferon</subject><subject>Interferon regulatory factor</subject><subject>IRF6</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Molecular modelling</subject><subject>Mutation</subject><subject>Nasopharyngeal carcinoma</subject><subject>Nasopharynx</subject><subject>Phenotypes</subject><subject>Radiation therapy</subject><subject>Squamous cells</subject><subject>Stem cell transplantation</subject><subject>Stem cells</subject><subject>Throat cancer</subject><subject>Transcription</subject><subject>Transcription factors</subject><subject>Tumor suppressor genes</subject><subject>Tumorigenesis</subject><issn>0304-3835</issn><issn>1872-7980</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kV9rFDEUxYModlv9BiIBX3yZNX8mmcmL0C5tLRQEqc8hk9zpZplJxiRb3C_i5zXLVh988OnC4XfOvclB6B0la0qo_LRbWxMmKGtGaFeldRVfoBXtO9Z0qicv0Ypw0ja85-IMnee8I4SIthOv0RlTlFLeqhX69bAF7OAJprjMEIqZcEkmZJv8UnwMeDS2xITvvt1IbEqBsDcFMr682twy_AgBMPxcEuR8hE1w2PlcfLDF18wDTjU65WrIBeZQMbxsIcRyWAD7gIPJcdmadAiPUFdbk6wPcTZv0KvRTBnePs8L9P3m-mHzpbn_enu3ubxvLCeiNL0bJeGKU-bU0EoqettLZcGOA-tkK5zjTigrDLFiaGEEZgfHbc-loMB6xi_Qx1PukuKPPeSiZ58tTJMJEPdZUyWpbFsqRUU__IPu4j6Fep1mRLWsl0yqSrUnyqaYc4JRL8nP9YGaEn3sTe_0qTd97O2oVrHa3j-H74cZ3F_Tn6Iq8PkEQP2NJw9JZ-shWHA-gS3aRf__Db8BfQiuUQ</recordid><startdate>20180901</startdate><enddate>20180901</enddate><creator>Xu, Liang</creator><creator>Huang, Tie-Jun</creator><creator>Hu, Hao</creator><creator>Wang, Meng-Yao</creator><creator>Shi, Si-Mei</creator><creator>Yang, Qin</creator><creator>Lin, Fen</creator><creator>Qiang, Yuan-Yuan</creator><creator>Mei, Yan</creator><creator>Lang, Yan-Hong</creator><creator>Li, Chang-Zhi</creator><creator>Peng, Li-Xia</creator><creator>Zheng, Li-Sheng</creator><creator>Huang, Jia-Ling</creator><creator>Li, Xin-Jian</creator><creator>Zhang, Shi-Jun</creator><creator>Qian, Chao-Nan</creator><creator>Huang, Bi-Jun</creator><general>Elsevier B.V</general><general>Elsevier Limited</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4292-1006</orcidid></search><sort><creationdate>20180901</creationdate><title>The developmental transcription factor IRF6 attenuates ABCG2 gene expression and distinctively reverses stemness phenotype in nasopharyngeal carcinoma</title><author>Xu, Liang ; Huang, Tie-Jun ; Hu, Hao ; Wang, Meng-Yao ; Shi, Si-Mei ; Yang, Qin ; Lin, Fen ; Qiang, Yuan-Yuan ; Mei, Yan ; Lang, Yan-Hong ; Li, Chang-Zhi ; Peng, Li-Xia ; Zheng, Li-Sheng ; Huang, Jia-Ling ; Li, Xin-Jian ; Zhang, Shi-Jun ; Qian, Chao-Nan ; Huang, Bi-Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c305t-8df6039312d9b46158c869cecfb27645dd3d59c5a0c5b4efe2cbd3c83651e2823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>ABCG2</topic><topic>ABCG2 gene</topic><topic>Animal models</topic><topic>Cancer stem cells</topic><topic>Cancer therapies</topic><topic>Cell growth</topic><topic>Cell proliferation</topic><topic>Cell self-renewal</topic><topic>Chemotherapy</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Gene expression</topic><topic>Grants</topic><topic>Interferon</topic><topic>Interferon regulatory factor</topic><topic>IRF6</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Molecular modelling</topic><topic>Mutation</topic><topic>Nasopharyngeal carcinoma</topic><topic>Nasopharynx</topic><topic>Phenotypes</topic><topic>Radiation therapy</topic><topic>Squamous cells</topic><topic>Stem cell transplantation</topic><topic>Stem cells</topic><topic>Throat cancer</topic><topic>Transcription</topic><topic>Transcription factors</topic><topic>Tumor suppressor genes</topic><topic>Tumorigenesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Liang</creatorcontrib><creatorcontrib>Huang, Tie-Jun</creatorcontrib><creatorcontrib>Hu, Hao</creatorcontrib><creatorcontrib>Wang, Meng-Yao</creatorcontrib><creatorcontrib>Shi, Si-Mei</creatorcontrib><creatorcontrib>Yang, Qin</creatorcontrib><creatorcontrib>Lin, Fen</creatorcontrib><creatorcontrib>Qiang, Yuan-Yuan</creatorcontrib><creatorcontrib>Mei, Yan</creatorcontrib><creatorcontrib>Lang, Yan-Hong</creatorcontrib><creatorcontrib>Li, Chang-Zhi</creatorcontrib><creatorcontrib>Peng, Li-Xia</creatorcontrib><creatorcontrib>Zheng, Li-Sheng</creatorcontrib><creatorcontrib>Huang, Jia-Ling</creatorcontrib><creatorcontrib>Li, Xin-Jian</creatorcontrib><creatorcontrib>Zhang, Shi-Jun</creatorcontrib><creatorcontrib>Qian, Chao-Nan</creatorcontrib><creatorcontrib>Huang, Bi-Jun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><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><collection>MEDLINE - Academic</collection><jtitle>Cancer letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Liang</au><au>Huang, Tie-Jun</au><au>Hu, Hao</au><au>Wang, Meng-Yao</au><au>Shi, Si-Mei</au><au>Yang, Qin</au><au>Lin, Fen</au><au>Qiang, Yuan-Yuan</au><au>Mei, Yan</au><au>Lang, Yan-Hong</au><au>Li, Chang-Zhi</au><au>Peng, Li-Xia</au><au>Zheng, Li-Sheng</au><au>Huang, Jia-Ling</au><au>Li, Xin-Jian</au><au>Zhang, Shi-Jun</au><au>Qian, Chao-Nan</au><au>Huang, Bi-Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The developmental transcription factor IRF6 attenuates ABCG2 gene expression and distinctively reverses stemness phenotype in nasopharyngeal carcinoma</atitle><jtitle>Cancer letters</jtitle><addtitle>Cancer Lett</addtitle><date>2018-09-01</date><risdate>2018</risdate><volume>431</volume><spage>230</spage><epage>243</epage><pages>230-243</pages><issn>0304-3835</issn><eissn>1872-7980</eissn><abstract>Nasopharyngeal carcinoma (NPC), which originates from the nasopharynx, is highly prevalent in Southern China and Southeast Asia, and more than 90% of all NPCs are non-keratinizing undifferentiated cells or poorly differentiated squamous cells. Cancer stem cells (CSCs) are capable of self-renewal and have differentiation potential. These properties form the basis of cancer initiation, development, and radiochemoresistance. However, the molecular mechanisms underlying NPC CSC maintenance remain poorly understood. Here, genomic expression profiling using our previously established monoclonal cellular and animal models revealed that interferon regulatory factor 6 (IRF6) was downregulated in highly metastatic NPC cells, cancer stem-like NPC cells and animal models. Functional assays revealed that elevated IRF6 expression suppressed cell proliferation, growth, CSCs properties and enhanced cell chemotherapeutic sensitivity. However, silencing IRF6 resulted in opposing effects. Moreover, we determined that as a tumor suppressor gene and transcription factor, IRF6 directly bound the upstream region of the ATP-binding cassette sub-family G member 2 (ABCG2) DNA element and suppressed target ABCG2 expression in NPC cells. Consistently, an inverse correlation was observed between the mRNA levels of IRF6 and ABCG2 in clinical NPC samples. With these results, we provide the first evidence that IRF6 directly targets the ABCG2 gene and selectively kills CSCs in NPC and that IRF6 may be a valuable tool for developing new CSC-targeted treatment strategies for undifferentiated NPC patients.
•IRF6 is initially found to be down regulated in our well established high-metastasis NPC cellular clone, and further series functional studies confirmed that IRF6 can inhibit the growth, migration, invasion, and metastasis of NPC cells.•Elevated IRF6 expression can enhance NPC chemotherapeutic sensitivity.•IRF6 down-regulates the expression of ABCG2 in NPC.•IRF6 can selectively kill nasopharyngeal carcinoma stem cells and overexpression of IRF6 is a promising approach for anti-stem cell targeted therapy.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>29111349</pmid><doi>10.1016/j.canlet.2017.10.016</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-4292-1006</orcidid></addata></record> |
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subjects | ABCG2 ABCG2 gene Animal models Cancer stem cells Cancer therapies Cell growth Cell proliferation Cell self-renewal Chemotherapy Deoxyribonucleic acid DNA Gene expression Grants Interferon Interferon regulatory factor IRF6 Metastases Metastasis Molecular modelling Mutation Nasopharyngeal carcinoma Nasopharynx Phenotypes Radiation therapy Squamous cells Stem cell transplantation Stem cells Throat cancer Transcription Transcription factors Tumor suppressor genes Tumorigenesis |
title | The developmental transcription factor IRF6 attenuates ABCG2 gene expression and distinctively reverses stemness phenotype in nasopharyngeal carcinoma |
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