| Literature DB >> 26797414 |
Tomoko Tadokoro1, Asahiro Morishita1, Shintaro Fujihara1, Hisakazu Iwama2, Toshiro Niki3, Koji Fujita1, Emiko Akashi1, Shima Mimura1, Kyoko Oura1, Teppei Sakamoto1, Takako Nomura1, Joji Tani1, Hisaaki Miyoshi1, Hirohito Yoneyama1, Takashi Himoto1, Mitsuomi Hirashima3, Tsutomu Masaki1.
Abstract
Gallbladder cancer (GBC) is the most common and aggressive type of biliary tract cancer. There are various histological types of GBC, and the vast majority of GBC cases are adenocarcinomas. Squamous and adenosquamous carcinomas are rare GBC subtypes that are traditionally considered to be more aggressive and to be associated with a poorer prognosis than adenocarcinoma. Galectin-9 (Gal-9), a tandem-repeat-type galectin, has been reported to induce apoptosis-mediated elimination of various cancers, including hepatocellular carcinoma, cholangiocarcinoma, and hematologic malignancies. Therefore, we investigated the antitumor effects of Gal-9 on GBC in vitro and in vivo. In our in vitro experiments, Gal-9 suppressed cell proliferation in various GBC cell lines but not in the OCUG-1 cell line, which represents a poorly differentiated type of adenosquamous carcinoma. Gal-9 induced the apoptosis of Gal-9-sensitive GBC cells by increasing the levels of caspase-cleaved keratin 18 and phosphorylated p53. However, Gal-9 did not affect the expression of various cell cycle-related proteins. In addition, Gal-9 suppressed tumor growth by implanted human GBC cells in a xenograft model. Furthermore, Gal-9 induced the phosphorylation of the Ephrin type-B receptor, and the microRNA (miRNA) expression profile was markedly altered by Gal-9. Based on these results, various miRNAs might contribute to the suppression of tumor growth. Our data reveal that Gal-9 suppresses the growth of GBC, possibly by inducing apoptosis and altering miRNA expression. Thus, Gal-9 might serve as a therapeutic agent for the treatment of GBC.Entities:
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Year: 2016 PMID: 26797414 DOI: 10.3892/ijo.2016.3347
Source DB: PubMed Journal: Int J Oncol ISSN: 1019-6439 Impact factor: 5.650