New anti-cancer role for PDK1 inhibitors: preventing resistance to tamoxifen
- PMID: 19061482
- DOI: 10.1042/BJ20082243
New anti-cancer role for PDK1 inhibitors: preventing resistance to tamoxifen
Abstract
Tamoxifen is one of the most prescribed anti-breast-cancer drugs, but tumours becoming resistant hinder its efficacy in the clinic. There is therefore great interest in developing strategies to reduce resistance and sensitize breast cancer cells to tamoxifen. A groundbreaking study by Iorns et al. published in this issue of the Biochemical Journal suggests that a signal transduction pathway controlled by PDK1 (phosphoinositide-dependent kinase 1) plays a crucial role in regulating the sensitivity of breast cancer cells to tamoxifen. The implications of this study are that PDK1 or PI3K (phosphoinositide 3-kinase), Akt (also known as protein kinase B), S6K (S6 kinase) and mTOR (mammalian target of rapamycin) inhibitors, already being developed for cancer therapy, are likely to have additional utility in sensitizing breast tumours to tamoxifen. In this commentary we also discuss the possibility that inhibiting the PDK1 pathway may help overcome acquired resistance to other anti-cancer treatments.
Comment on
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Parallel RNAi and compound screens identify the PDK1 pathway as a target for tamoxifen sensitization.Biochem J. 2009 Jan 1;417(1):361-70. doi: 10.1042/BJ20081682. Biochem J. 2009. PMID: 18976239
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