Interaction between DNA damage response and autophagy in colorectal cancer

Elmira Roshani-Asl1, Behzad Mansori2, Ali Mohammadi3

  • 1Department of Biochemistry, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran; Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Gene
|January 10, 2020
PubMed

Insights

DNA damage response (DDR) and autophagy are crucial for genome stability. Their complex interplay influences cancer development, particularly colorectal cancer, offering potential therapeutic targets.

Area of Science:

  • Molecular Biology
  • Cellular Biology
  • Oncology

Background:

  • DNA damage poses a significant threat to genome stability.
  • The DNA Damage Response (DDR) is a critical signaling pathway that maintains genome integrity.
  • Autophagy, a cellular degradation process, is increasingly recognized for its role in cancer pathogenesis.

Purpose of the Study:

  • To review the intricate crosstalk between DNA Damage Response (DDR) and autophagy.
  • To elucidate the role of this interplay in the pathogenesis of various human cancers.
  • To focus specifically on the role of DDR and autophagy in colorectal cancer development.

Main Methods:

  • Literature review of recent studies on DDR and autophagy.
  • Analysis of signaling pathways involving DDR and autophagy.
  • Examination of the role of these pathways in cancer models.

Main Results:

  • DDR signaling can activate autophagy, suggesting autophagy as an effector of DDR.
  • Autophagy can also regulate components of the DDR pathway.
  • The interplay between DDR and autophagy is implicated in the development of malignancies, including colorectal cancer.

Conclusions:

  • The crosstalk between DDR and autophagy is a critical factor in cancer pathogenesis.
  • Understanding this relationship may provide a basis for novel therapeutic strategies against colorectal cancer.
  • Further research into the DDR-autophagy axis is warranted for cancer treatment.

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