Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6075606 | Journal of Investigative Dermatology | 2015 | 9 Pages |
Abstract
IGF II mRNA-binding protein 3 (IMP-3) has been reported to be a marker of melanoma progression. However, the mechanisms by which it impacts melanoma are incompletely understood. In this study, we investigate the clinical significance of IMP-3 in melanoma progression and also its underlying mechanisms. We found that IMP-3 expression was much higher in advanced-stage/metastatic melanomas and that it was associated with a poor prognosis (P=0.001). Univariate analysis showed that IMP-3 expression was associated with stage III/IV melanomas (odds ratio=5.40, P=0.031) and the acral lentiginous subtype (odds ratio=3.93, P=0.0034). MeWo cells with overexpression of IMP-3 showed enhanced proliferation and migration and significantly increased tumorigenesis and metastatic ability in nude mice. We further demonstrated that IMP-3 could bind and enhance the stability of the mRNA of high mobility group AT-hook 2 (HMGA2). It was also confirmed that IMP-3 had an important role in melanoma invasion and metastasis through regulating HMGA2 mRNA expression. IMP-3 expression was positively correlated with HMGA2 expression in melanoma cells and also in melanoma tissues. Our results show that IMP-3 expression is a strong prognostic factor for melanoma, especially acral lentiginous melanoma.
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Authors
Yi-Shuan Sheen, Yi-Hua Liao, Ming-Hsien Lin, Chia-Ying Chu, Bing-Ying Ho, Meng-Chen Hsieh, Pin-Chun Chen, Shih-Ting Cha, Yung-Ming Jeng, Cheng-Chi Chang, Hsien-Ching Chiu, Shiou-Hwa Jee, Min-Liang Kuo, Chia-Yu Chu,