Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 이영식 | - |
dc.date.accessioned | 2018-11-07T04:42:14Z | - |
dc.date.available | 2018-11-07T04:42:14Z | - |
dc.date.issued | 2008-04 | - |
dc.identifier.citation | GLYCOBIOLOGY, v. 18, No. 5, Page. 395-407 | en_US |
dc.identifier.issn | 0959-6658 | - |
dc.identifier.uri | https://academic.oup.com/glycob/article/18/5/395/1988068 | - |
dc.identifier.uri | https://repository.hanyang.ac.kr/handle/20.500.11754/80280 | - |
dc.description.abstract | Ganglioside GM3 inhibits the growth of several cancer cells and induces cell cycle arrest by regulating cellular signal pathways. Our previous results have shown that GM3 suppresses tumor suppressor PTEN-mediated cancer cell proliferation. However, the precise molecular mechanism(s) for the transcriptional regulation of a PTEN gene induced by GM3 remains unclear. Here, we show, for the first time, that GM3 induces transcription factor AP-2 alpha-mediated PTEN expression in colon cancer cells. The enhanced expression of PTEN by GM3 in both HCT116 and p53- HCT116 cells has been shown to be not associated with p53 function. Thus, to further determine the mechanism underlying the regulation of PTEN gene expression by GM3, we characterized the promoter region of the PTEN gene. Promoter analysis of the 5'-flanking region of the PTEN gene showed that the region between -1175 and -1077 from the translational initiation site, which contains the AP-2 alpha binding site, functions as the GM3-inducible promoter in colon cancer cells. Furthermore, gel shift assays, site-directed mutagenesis, and chromatin immunoprecipitation assay obviously indicated that the AP-2 alpha is essential for the expression of PTEN in GM3-stimulated colon cancer cells. Moreover, siRNA against AP-2 alpha diminished the enhancement of AP-2 alpha and PTEN expressions in GM3-induced colon cancer cells. The transient expression of AP-2 alpha also results in the induction of PTEN transcription in AP-2 alpha-negative colon cancer cells. Additionally, GM3 induced AP-2 alpha-mediated PTEN expression through the inhibition of autocrine-ligand-mediated EGFR activation. These results suggest that the AP-2 alpha transcription factor is required for the ganglioside GM3-stimulated transcriptional regulation of the PTEN gene. | en_US |
dc.description.sponsorship | This study was in part supported by 21C Frontier Research for Human Genome, KOSEF, funded by the Korean Government (no. FG-1-2 to C.-H. Kim) and the Korea Health 21 R&D Project, Ministry of Health and Welfare, Korea (A060052). H.J. Choi is a recipient of BK21 Biological Science of SKKU. | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | OXFORD UNIV PRESS INC | en_US |
dc.subject | GROWTH-FACTOR RECEPTOR | en_US |
dc.subject | TUMOR-SUPPRESSOR PTEN | en_US |
dc.subject | CELL-CYCLE PROGRESSION | en_US |
dc.subject | FACTOR AP-2 | en_US |
dc.subject | CANCER-CELLS | en_US |
dc.subject | ACTIVATOR PROTEIN-2-ALPHA | en_US |
dc.subject | APOPTOSIS INDUCTION | en_US |
dc.subject | NEGATIVE REGULATION | en_US |
dc.subject | MAMMARY-CARCINOMA | en_US |
dc.subject | COWDEN-DISEASE | en_US |
dc.subject | AP-2α | en_US |
dc.subject | colon cancer cells | en_US |
dc.subject | ganglioside GM3 | en_US |
dc.subject | PTEN | en_US |
dc.subject | transcriptional regulation | en_US |
dc.title | The AP-2α transcription factor is required for the ganglioside GM3-stimulated transcriptional regulation of a PTEN gene | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1093/glycob/cwn016 | - |
dc.relation.journal | GLYCOBIOLOGY | - |
dc.contributor.googleauthor | Choi, Hee-Jung | - |
dc.contributor.googleauthor | Chung, Tae-Wook | - |
dc.contributor.googleauthor | Kim, Seok-Jo | - |
dc.contributor.googleauthor | Cho, Soo-Young | - |
dc.contributor.googleauthor | Lee, Young-Seek | - |
dc.contributor.googleauthor | Lee, Young-Choon | - |
dc.contributor.googleauthor | Ko, Jeong-Heon | - |
dc.contributor.googleauthor | Kim, Cheorl-Ho | - |
dc.relation.code | 2008203496 | - |
dc.sector.campus | E | - |
dc.sector.daehak | COLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY[E] | - |
dc.sector.department | DEPARTMENT OF MOLECULAR AND LIFE SCIENCE | - |
dc.identifier.pid | yslee | - |
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