Gadd45a protects against UV irradiation-induced skin tumors, and promotes apoptosis and stress signaling via MAPK and p53

Author:

Hildesheim, J.

Bulavin, D. V.

Anver, M. R.

Alvord, W. G.

Hollander, M. C.

Vardanian, L.

Fornace, A. J.
Author Address

NCI, Gene Response Sect, Ctr Canc Res, NIH, Bldg 37,Room 6144,37 Convent Dr,MSC 4255, Bethesda, MD 20892 USA NCI, Gene Response Sect, Ctr Canc Res, NIH, Bethesda, MD 20892 USA Sci Applicat Int Corp, Pathol Histotechnol Lab, Frederick, MD 21702 USA NCI, Data Management Serv, Frederick, MD 21702 USA Fornace AJ NCI, Gene Response Sect, Ctr Canc Res, NIH, Bldg 37,Room 6144,37 Convent Dr,MSC 4255, Bethesda, MD 20892 USA

Abstract:

Skin cancer is the most frequent form of malignancy in the world, and UV radiation is the primary environmental carcinogen responsible for its development. Herein we demonstrate that Gadd45a is a critical factor protecting the epidermis against UV radiation-induced tumorigenesis by promoting damaged keratinocytes to undergo apoptosis and/or cell cycle arrest, two crucial events that prevent the expansion of mutant or deregulated cells. Whereas Gadd45a has been implicated in cell cycle arrest, apoptosis, and DNA repair, to determine the physiological function of endogenous Gadd45a after genotoxic stress, the skin of Gadd45a-null mice was targeted with UV radiation. We report that Gadd45a induces apoptosis and cell cycle arrest by maintaining p38 and c-JNK MAPK activation in keratinocytes. The absence of Gadd45a results in loss of sustained p38/JNK MAPK activity beyond 15-30 min after UV radiation that leads to inadequate p53 activation and loss of normal activation of G(1) and G(2) checkpoints. Moreover, loss of Gadd45a dramatically reduces UV-induced apoptotic keratinocytes, "sunburn cells." Consequently, Gadd45a-null mice are more prone to tumors relative to wild-type mice. Therefore, we conclude that Gadd45a, like p53, is a key component protecting skin against UV-induced tumors.

See More

Platinum Publication

Author Address