Objective: MicroRNAs (miRNAs) play important roles in carcinogenesis. The aim of the present study wasto explore the effects of miR-181b on gastric cancer. Methods: The expression level of miR-181b was quantifiedby qRT-PCR. MTT, flow cytometry and matrigel invasion assays were used to test proliferation, apoptosis andinvasion of miR-181b stable transfected gastric cancer cells. Results: miR-181b was aberrantly overexpressed ingastric cancer cells and primary gastric cancer tissues. Further experiments demonstrated inducible expression ofmiR-181b by Helicobacter pylori treatment. Cell proliferation, migration and invasion in the gastric cancer cellswere significantly increased after miR-181b transfection and apoptotic cells were also increased. Furthermore,overexpression of miR-181b downregulated the protein level of tissue inhibitor of metalloproteinase 3 (TIMP3). Conclusion: The upregulation of miR-181b may play an important role in the progress of gastric cancer andmiR-181b maybe a potential molecular target for anticancer therapeutics of gastric cancer.
(2012). miR-181b as a Potential Molecular Target for Anticancer Therapy of Gastric Neoplasms. Asian Pacific Journal of Cancer Prevention, 13(5), 2263-2267.
MLA
. "miR-181b as a Potential Molecular Target for Anticancer Therapy of Gastric Neoplasms". Asian Pacific Journal of Cancer Prevention, 13, 5, 2012, 2263-2267.
HARVARD
(2012). 'miR-181b as a Potential Molecular Target for Anticancer Therapy of Gastric Neoplasms', Asian Pacific Journal of Cancer Prevention, 13(5), pp. 2263-2267.
VANCOUVER
miR-181b as a Potential Molecular Target for Anticancer Therapy of Gastric Neoplasms. Asian Pacific Journal of Cancer Prevention, 2012; 13(5): 2263-2267.