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conferenceseries

.com

June 26-27, 2017 San Diego, USA

13

th

International conference on

Pathology and Molecular Diagnosis

Volume 7, Issue 2 (Suppl)

J Clin Exp Pathol, an open access journal

ISSN:2161-0681

Pathology and Molecular Diagnosis 2017

June 26-27, 2017

Studies on miR-885-5p as a potential serum biomarker of HCC and its suppresses metastasis effects

Yaping Tian, Junhao Gui

and

Zhuhong Zhang

Chinese PLA General Hospital, China

C

irculating miRNAs (microRNAs) are emerging as promising biomarkers for several pathological conditions, and the aim

of this study was to investigate the feasibility of using serum miRNAs as biomarkers for liver pathologies. Real-time qPCR

(quantitative PCR)-based TaqMan MicroRNA arrays were first employed to profile miRNAs in serum pools from patients with

HCC (hepatocellular carcinoma) or LC (liver cirrhosis) and from healthy controls. Five miRNAs (i.e. miR-885-5p, miR-574-3p,

miR-224, miR-215 and miR-146a) that were up-regulated in the HCC and LC serum pools were selected and further quantified

using real-time qPCR in patients with HCC, LC, CHB (chronic hepatitis B) or GC (gastric cancer) and in normal controls.

And then the miR-885-5p in HCC metastasis have been studied. The results demonstrated that the expression of miR-885-5p

negatively correlated with the invasive and metastatic capabilities of human HCC tissue samples and cell lines. Overexpression

of miR-885-5p decreased metastasis of HCC cells

in vitro

and

in vivo

. Inhibition of miR-885-5p improved proliferation of

non-metastatic HCC cells. Furthermore, we disclosed that miR-885-5p targeted gene encoding β-catenin CTNNB1, leading

to decreased activity of the Wnt/β-catenin signaling pathway. The present study indicates that miR-885-5p suppresses the

metastasis of HCC and inhibits Wnt/β-catenin signaling pathway by its CTNNB1 target, which suggests that miR-885-5p to be

a promising negative regulator of HCC progression and as a novel therapeutic agent to treat HCC.

Biography

Yaping Tian is a Professor of Department of Clinical Biochemistry, Chinese PLA General Hospital and Military Medical School. He is also a Professor of Nankai

University, and Tsinghua University. He received his Master’s degree in Medicine from Chinese PLA Postgraduate Medical School in 1989 and PhD from Academy

of Military Medical Sciences in 1993. He had been trained as Postdoctoral Fellow for 2 years (1995-1997) in The Queen Elizabeth Hospital, Australia. He has been

focusing on the study of specific serum proteomic profiles and genetic signatures in different diseases, especially on cancer and cardiovascular diseases. He also

focused on the studies of antioxidants in herbal medicine and free radical biology. He has received more than 20 grants and published more than 300 scientific

papers in peer-reviewed journals. He is on the Editorial Boards of several journals and the honor Chairman of the Clinical Biochemistry and Applied Molecular

Biology Association, CSBMB.

tianyp@301hospital.com.cn

Yaping Tian et al., J Clin Exp Pathol 2017, 7:2 (Suppl)

DOI: 10.4172/2161-0681-C1-034