癌症
转录组
癌症研究
癌变
细胞凋亡
癌细胞
抑制器
医学
生物
基因
内科学
基因表达
遗传学
作者
Jin Muk Kang,Sujin Park,Staci Jakyong Kim,Hyo-Jung Kim,Bona Lee,Junil Kim,Jinah Park,Shin Tae Kim,Han‐Kwang Yang,Woo Ho Kim,Seong‐Jin Kim
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2015-06-05
卷期号:75 (15): 3087-3097
被引量:51
标识
DOI:10.1158/0008-5472.can-14-3751
摘要
Abstract Recent advances in genome and transcriptome analysis have contributed to the identification of many potential cancer-related genes. Furthermore, biological and clinical investigations of the candidate genes provide us with a better understanding of carcinogenesis and development of cancer treatment. Here, we report a novel role of KIAA1324 as a tumor suppressor in gastric cancer. We observed that KIAA1324 was downregulated in most gastric cancers from transcriptome sequencing data and found that histone deacetylase was involved in the suppression of KIAA1324. Low KIAA1324 levels were associated with poor prognosis in gastric cancer patients. In the xenograft model, KIAA1324 significantly reduced tumor formation of gastric cancer cells and decreased development of preformed tumors. KIAA1324 also suppressed proliferation, invasion, and drug resistance and induced apoptosis in gastric cancer cells. Through protein interaction analysis, we identified GRP78 (glucose-regulated protein 78 kDa) as a KIAA1324-binding partner. KIAA1324 blocked oncogenic activities of GRP78 by inhibiting GRP78–caspase-7 interaction and suppressing GRP78-mediated AKT activation, thereby inducing apoptosis. In conclusion, our study reveals a tumor suppressive role of KIAA1324 via inhibition of GRP78 oncoprotein activities and provides new insight into the diagnosis and treatment of gastric cancer. Cancer Res; 75(15); 3087–97. ©2015 AACR.
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