| Literature DB >> 23007279 |
Hai-Ji Sun1, Yun-Jian Liu, Na Li, Zhi-Yong Sun, Hai-Wang Zhao, Chen Wang, Hui Li, Fang-Ming Ma, Song-Mei Shi, Xiao-Qiu Xu, Zhe-Yu Chen, Shu-Hong Huang.
Abstract
The novel member of the Rab family of GTPases, Rab23, is an essential negative regulator of the Sonic hedgehog (Shh) signaling pathway. Loss of function mutation of the Rab23 gene causes abnormal development of the neural tube in mice and in certain human congenital diseases. The aberrant overexpression of Rab23 has been associated with various diseases, such as gastric, hepatocellular and lung cancer. The exact function of Rab23 in hepatocellular carcinomas (HCCs), however, remains unknown. Previously, we reported the abnormal sublocalization of Rab23 in lung cancers. In the current study, we investigated the role of Rab23 in HCCs. We report the distinct sublocalization pattern of Rab23 in HCC cell lines. This difference depends on the GDP/GTP-binding form, and inhibition of the Rab23 cycle decreases the expression and nuclear localization of Gli1.Entities:
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Year: 2012 PMID: 23007279 DOI: 10.3892/mmr.2012.1094
Source DB: PubMed Journal: Mol Med Rep ISSN: 1791-2997 Impact factor: 2.952