| pubmed-article:19698176 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19698176 | lifeskim:mentions | umls-concept:C0086661 | lld:lifeskim |
| pubmed-article:19698176 | lifeskim:mentions | umls-concept:C1518174 | lld:lifeskim |
| pubmed-article:19698176 | lifeskim:mentions | umls-concept:C2931822 | lld:lifeskim |
| pubmed-article:19698176 | lifeskim:mentions | umls-concept:C1155873 | lld:lifeskim |
| pubmed-article:19698176 | lifeskim:mentions | umls-concept:C0086982 | lld:lifeskim |
| pubmed-article:19698176 | lifeskim:mentions | umls-concept:C0205263 | lld:lifeskim |
| pubmed-article:19698176 | pubmed:dateCreated | 2009-9-14 | lld:pubmed |
| pubmed-article:19698176 | pubmed:abstractText | apogossypolone (ApoG2) is a novel derivate of gossypol. We previously have reported that ApoG2 is a promising compound that kills nasopharyngeal carcinoma (NPC) cells by inhibiting the antiapoptotic function of Bcl-2 proteins. However, some researchers demonstrate that the antiproliferative effect of gossypol on breast cancer cells is mediated by induction of cell cycle arrest. So this study was aimed to investigate the effect of ApoG2 on cell cycle proliferation in NPC cells. | lld:pubmed |
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| pubmed-article:19698176 | pubmed:language | eng | lld:pubmed |
| pubmed-article:19698176 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19698176 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:19698176 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:19698176 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19698176 | pubmed:issn | 1479-5876 | lld:pubmed |
| pubmed-article:19698176 | pubmed:author | pubmed-author:HuntSS | lld:pubmed |
| pubmed-article:19698176 | pubmed:author | pubmed-author:ZengYi-XinYX | lld:pubmed |
| pubmed-article:19698176 | pubmed:author | pubmed-author:ZhuXiao-FengX... | lld:pubmed |
| pubmed-article:19698176 | pubmed:author | pubmed-author:YangDajunD | lld:pubmed |
| pubmed-article:19698176 | pubmed:author | pubmed-author:HuZhe-YuZY | lld:pubmed |
| pubmed-article:19698176 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19698176 | pubmed:volume | 7 | lld:pubmed |
| pubmed-article:19698176 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19698176 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19698176 | pubmed:pagination | 74 | lld:pubmed |
| pubmed-article:19698176 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:19698176 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19698176 | pubmed:articleTitle | ApoG2 induces cell cycle arrest of nasopharyngeal carcinoma cells by suppressing the c-Myc signaling pathway. | lld:pubmed |
| pubmed-article:19698176 | pubmed:affiliation | State Key Laboratory of Oncology in South China and Department of Experimental Research, Sun Yat-sen University Cancer Center, Guangzhou, PR China. huzheyu24@gmail.com | lld:pubmed |
| pubmed-article:19698176 | pubmed:publicationType | Journal Article | lld:pubmed |
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