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- W1844690031 abstract "// Zheng Li 1 , Xin Yu 1 , Yang Wang 2 , Jianxiong Shen 1 , William Ka Kei Wu 3 , Jinqian Liang 1 , Fan Feng 1 1 Department of Orthopaedic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China 2 Department of Abdominal Surgery, Cancer Institute and Cancer Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China 3 Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong, Hong Kong, China Correspondence to: Jianxiong Shen, e-mail: shenjianxiong@medmail.com.cn Keywords: Gastric cancer, MicroRNAs, miR-329, TIAM1 Received: November 09, 2014 Accepted: November 16, 2014 Published: February 11, 2015 ABSTRACT Gastric cancer (GC) is one of the most common malignant tumors worldwide. Emerging evidence has shown that abnormal microRNAs (miRNAs) expression is involved in tumorigenesis. MiR-329 was previously reported to act as a tumor suppressor or oncogene in some types of cancer. However, its function in gastric cancer (GC) is unclear. Here, we found that miR-329 was down-regulated in GC compared with adjacent controls. Enforced expression of miR-329 inhibited proliferation, migration and invasion of gastric cancer cells in vitro . We identified T lymphoma invasion and metastasis 1 (TIAM1) gene as potential target of miR-329. MiR-329 levels inversely correlated with TIAM1 expression in GC. Importantly, TIAM1 rescued the miR-329-mediated inhibition of cell invasion and proliferation. Finally, reintroduction of miR-329 significantly inhibited tumor formation of GC in the xenograft mice. Our findings suggest that miR-329 is a tumor suppressor and potential therapeutic target of GC." @default.
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- W1844690031 date "2015-02-19" @default.
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- W1844690031 title "By downregulating TIAM1 expression, microRNA-329 suppresses gastric cancer invasion and growth" @default.
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- W1844690031 doi "https://doi.org/10.18632/oncotarget.2755" @default.
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