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Dermatology - Molecular Biology - Oncology


JWA Deficiency Suppresses Dimethylbenz[a]Anthracene-Phorbol Ester Induced Skin Papillomas via Inactivation of MAPK Pathway in Mice
Published: Monday, March 26, 2012
Author: Zhenghua Gong et al.

by Zhenghua Gong, Yaowei Shi, Ze Zhu, Xuan Li, Yang Ye, Jianbing Zhang, Aiping Li, Gang Li, Jianwei Zhou

Our previous studies indicated that JWA plays an important role in DNA damage repair, cell migration, and regulation of MAPKs. In this study, we investigated the role of JWA in chemical carcinogenesis using conditional JWA knockout (JWA?2/?2) mice and two-stage model of skin carcinogenesis. Our results indicated that JWA?2/?2 mice were resistant to the development of skin papillomas initiated by 7, 12-dimethylbenz(a)anthracene (DMBA) followed by promotion with 12-O-tetradecanoylphorbol-13-acetate (TPA). In JWA?2/?2 mice, the induction of papilloma was delayed, and the tumor number and size were reduced. In primary keratinocytes from JWA?2/?2 mice, DMBA exposure induced more intensive DNA damage, while TPA-promoted cell proliferation was reduced. The further mechanistic studies showed that JWA deficiency blocked TPA-induced activation of MAPKs and its downstream transcription factor Elk1 both in vitro and in vivo. JWA?2/?2 mice are resistance to tumorigenesis induced by DMBA/TPA probably through inhibition of transcription factor Elk1 via MAPKs. These results highlight the importance of JWA in skin homeostasis and in the process of skin tumor development.
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