Let‐7 repression leads to HMGA2 overexpression in uterine leiomyosarcoma

Overexpression of HMGA2 is common in uterine leiomyomas (ULM). The expression of HMGA2 in its malignant counterpart – uterine leiomyosarcomas (ULMS) remains undetermined. Recently it has been shown that repression of HMGA2 by microRNA let‐7s is a critical molecular regulatory mechanism associated wi...

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Veröffentlicht in:Journal of cellular and molecular medicine 2009-09, Vol.13 (9b), p.3898-3905
Hauptverfasser: Shi, Guizhi, Perle, Mary Ann, Mittal, Khush, Chen, Hua, Zou, Xuanyi, Narita, Masashi, Hernando, Eva, Lee, Peng, Wei, Jian‐Jun
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Sprache:eng
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Zusammenfassung:Overexpression of HMGA2 is common in uterine leiomyomas (ULM). The expression of HMGA2 in its malignant counterpart – uterine leiomyosarcomas (ULMS) remains undetermined. Recently it has been shown that repression of HMGA2 by microRNA let‐7s is a critical molecular regulatory mechanism associated with tumour growth in many tumours and cell types, including leiomyomas. To test whether HMGA2 and let‐7s play a role in ULMS, we examined the levels of endogenous HMGA2 and let‐7 expression and found a significant correlation between these two molecules in a case‐matched cohort of human ULMS. We found that overexpression of HMGA2 and let‐7‐mediated HMGA2 repression is a relevant molecular alteration in ULMS. Disrupting the control of HMGA2 and let‐7 pairs promotes ULMS cell growth in vitro.
ISSN:1582-1838
1582-4934
DOI:10.1111/j.1582-4934.2008.00541.x