DNA alkylation damage and autophagy induction.

Mutat Res

Departamento de Biofísica/Centro de Biotecnologia, Universidade Federal do Rio Grande do Sul, Avenida Bento Gonçalves, 9500, CEP 91501-970 Porto Alegre, RS, Brazil; Instituto de Biotecnologia, Universidade de Caxias do Sul, Rua Francisco Getúlio Vargas, 1130, CEP 95070-560 Caxias do Sul, RS, Brazil. Electronic address:

Published: February 2014

AI Article Synopsis

  • Many alkylating agents have been used successfully as chemotherapy drugs, causing significant DNA damage and triggering complex cellular responses for survival and repair.
  • Induction of autophagy in cancer cells after treatment can either delay cell death, leading to chemoresistance, or contribute to cell death, depending on the damage and context.
  • The review focuses on the primary alkylating agents in oncology and explores how they affect cellular responses, especially the role of autophagy in this process.

Article Abstract

Many alkylating agents are used as chemotherapeutic drugs and have a long history of clinical application. These agents inflict a wide range of DNA damage resulting in a complex cellular response. After DNA damage, cells trigger a series of signaling cascades promoting cellular survival and cell cycle blockage which enables time for DNA repair to occur. More recently, induction of autophagy has been observed in cancer cells after treatment with different DNA-targeted anticancer drugs, including alkylating agents. Several studies have demonstrated that induction of autophagy after DNA damage delays apoptotic cell death and may therefore lead to chemoresistance, which is the limiting factor for successful chemotherapy. On the other hand, depending on the extent of damage and the cellular context, the induction of autophagy may also contribute to cell death. Given these conflicting results, many studies have been conducted to better define the role of autophagy in cancer cells in response to chemotherapy. In this review, we describe the main alkylating agents used in clinical oncology as well as the cellular response they evoke with emphasis on autophagy.

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http://dx.doi.org/10.1016/j.mrrev.2013.07.001DOI Listing

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