| Literature DB >> 26199092 |
Ling Chen1, Lingqiang Min1, Xuefei Wang1, Junjie Zhao1, Hua Chen2, Jing Qin1, Weidong Chen1, Zhenbin Shen1, Zhaoqing Tang1, Qiangjun Gan1, Yuanyuan Ruan3, Yihong Sun4, Xinyu Qin4, Jianxin Gu5.
Abstract
Gastric cancer remains the third leading cause of cancer-related mortality worldwide, and invasion and metastasis of gastric cancer represent the major reason for its poor prognosis. In this study, we found that loss of the receptor for activated C-kinase 1 (RACK1) promoted the metastasis of gastric cancer by enhancing the autocrine expression of IL8 in vitro and in vivo. microRNA (miRNA; miR) array identified that RACK1 modulated the expression of a series of miRNAs, including the miR-302 cluster, and RACK1 modulated the IL8 expression and tumor invasion through miRNA-302c. Moreover, upregulation of IL8 in turn decreased the level of miRNA-302c and induced IL8 expression in a feedback manner. Tissue microarray also indicated that RACK1 was correlated with invasion/metastasis phenotype, IL8 expression, as well as 5-year survival in clinical cases of gastric cancer. Together, our results imply that loss of RACK1 in gastric cancer links epigenetics to inflammatory cytokines to promote tumor metastasis. ©2015 American Association for Cancer Research.Entities:
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Year: 2015 PMID: 26199092 DOI: 10.1158/0008-5472.CAN-14-3690
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701