New anti-cancer role for PDK1 inhibitors: preventing resistance to tamoxifen

Author:

Peifer Christian1,Alessi Dario R.1

Affiliation:

1. MRC Protein Phosphorylation Unit, School of Life Sciences, MSI/WTB Complex, University of Dundee, Dow Street, Dundee DD1 5EH, Scotland, U.K.

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.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference19 articles.

1. Parallel RNAi and compound screens identify the PDK1 pathway as a target for tamoxifen sensitisation;Iorns;Biochem. J.,2008

2. PDK1, the master regulator of AGC kinase signal transduction;Mora;Semin. Cell Dev. Biol.,2004

3. PI3K pathway alterations in cancer: variations on a theme;Yuan;Oncogene,2008

4. Transformation of mammary epithelial cells by 3-phosphoinositide-dependent protein kinase-1 (PDK1) is associated with the induction of protein kinase Cα;Zeng;Cancer Res.,2002

5. Hypomorphic mutation of PDK1 suppresses tumorigenesis in PTEN+/− mice;Bayascas;Curr. Biol.,2005

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