Oncotarget

Research Papers:

TMEM16A overexpression contributes to tumor invasion and poor prognosis of human gastric cancer through TGF-β signaling

Fang Liu _, Qing-Hua Cao, De-Jian Lu, Bin Luo, Xiao-Fang Lu, Rong-Cheng Luo and Xiao-Guang Wang

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Oncotarget. 2015; 6:11585-11599. https://doi.org/10.18632/oncotarget.3412

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Abstract

Fang Liu1,2,3,*, Qing-Hua Cao4,*, De-Jian Lu2,*, Bin Luo2, Xiao-Fang Lu4, Rong-Cheng Luo3, Xiao-Guang Wang2

1Department of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China

2Faculty of Forensic Medicine, ZhongShan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China

3Cancer Center and Traditional Chinese Medicine-Integrated Hospital, Southern Medical University, Guangzhou 510315, China

4Department of Pathology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou 510080, China

*These authors have contributed equally to this work

Correspondence to:

Xiao-Guang Wang, e-mail: [email protected]

Rong-Cheng Luo, e-mail: [email protected]

Keywords: TMEM16A, invasion, prognosis, gastric cancer, TGF-β

Received: October 02, 2014     Accepted: February 19, 2015     Published: March 23, 2015

ABSTRACT

TMEM16A is a newly identified calcium activated chloride channel, and has been reported to be overexpressed by various solid malignant cancers to promote proliferation and invasion, yet little is known about its role in gastric cancer(GC). Therefore, we investigated the role of TMEM16A in GC and its clinical significance by a retrospective analysis of 367 GC patients, and in vitro study was performed for validation and underlying molecular mechanism.

TMEM16A was significantly upregulated and amplified in GC tissues, and its overexpression was positively correlated with disease stage, negatively with patient survival and identified as an independent prognostic factor for patient outcome. A negative correlation between TMEM16A and E-cadherin was found in 367 GC specimens. TMEM16A silencing significantly decreased calcium activated chloride currents, impaired TGF-β secretion, reduced E-cadherin expression, and inhibited the migration and invasion without affecting proliferation of GC cells (AGS and BGC-823). Supplement of TGF-β reverted the effects of TMEM16A silencing on E-cadherin expression, cell migration and invasion.

In conclusion, TMEM16A promotes invasion and metastasis in GC, and might be a novel prognostic biomarker and potential therapeutic target in the treatment of GC.


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