Proteins from the DNA Damage Response: Regulation, Dysfunction, and Anticancer Strategies

Caroline Molinaro1, Alain Martoriati1, Katia Cailliau1

  • 1Univ. Lille, CNRS, UMR 8576-UGSF-Unité de Glycobiologie Structurale et Fonctionnelle, F-59000 Lille, France.

Cancers
|August 7, 2021
PubMed

Insights

Cells utilize DNA damage response (DDR) pathways to maintain genome integrity. Targeting these DDR mechanisms offers promising new strategies for cancer therapy and treatment.

Area of Science:

  • Molecular Biology
  • Genetics
  • Cancer Research

Background:

  • Cells possess intricate DNA damage response (DDR) pathways to manage genotoxic stress.
  • These pathways are vital for genome maintenance, cell cycle control, and programmed cell death, ensuring genetic stability.
  • Dysfunctional DDR pathways are implicated in various diseases, including cancer.

Purpose of the Study:

  • To explore the role of DNA damage response (DDR) pathways in maintaining genome stability.
  • To investigate the potential of leveraging DDR mechanisms for targeted cancer therapy.

Main Methods:

  • The study reviews the fundamental principles and mechanisms of DNA damage response (DDR) pathways.
  • It examines the implications of DDR alterations in disease pathogenesis and cancer formation.
  • Technological advancements enabling the application of DDR principles in cancer treatment are discussed.

Main Results:

  • DNA damage response (DDR) pathways are crucial for genome stability and diversity.
  • Mutations in DDR proteins can lead to diseases and tumor formation.
  • New therapeutic strategies targeting cancer cells by exploiting DDR mechanisms are emerging.

Conclusions:

  • DNA damage response (DDR) pathways are essential for cellular health and preventing diseases like cancer.
  • Targeting DDR pathways represents a promising frontier in cancer treatment, with potential for combination therapies to maximize efficacy.

Related Concept Videos

DNA Damage can Stall the Cell Cycle02:37

DNA Damage can Stall the Cell Cycle

In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
9.6K
DNA Damage Can Stall the Cell Cycle02:37

DNA Damage Can Stall the Cell Cycle

2.8K
Overview of DNA Repair02:25

Overview of DNA Repair

In order to be passed through generations, genomic DNA must be undamaged and error-free. However, every day, DNA in a cell undergoes several thousand to a million damaging events by natural causes and external factors. Ionizing radiation such as UV rays, free radicals produced during cellular respiration, and hydrolytic damage from metabolic reactions can alter the structure of DNA. Damages caused include single-base alteration, base dimerization, chain breaks, and cross-linkage.
Chemically...
32.3K
Overview of DNA Repair02:25

Overview of DNA Repair

8.4K
Nucleotide Excision Repair01:38

Nucleotide Excision Repair

DNA Distortion and Damage
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
4.2K
Nucleotide Excision Repair01:08

Nucleotide Excision Repair

Overview
38.3K