Targeting DNA Damage Response and Repair to Enhance Therapeutic Index in Cisplatin-Based Cancer Treatment

Int J Mol Sci. 2021 Jul 30;22(15):8199. doi: 10.3390/ijms22158199.

Abstract

Platinum-based chemotherapies, such as cisplatin, play a large role in cancer treatment. The development of resistance and treatment toxicity creates substantial barriers to disease control, yet. To enhance the therapeutic index of cisplatin-based chemotherapy, it is imperative to circumvent resistance and toxicity while optimizing tumor sensitization. One of the primary mechanisms by which cancer cells develop resistance to cisplatin is through upregulation of DNA repair pathways. In this review, we discuss the DNA damage response in the context of cisplatin-induced DNA damage. We describe the proteins involved in the pathways and their roles in resistance development. Common biomarkers for cisplatin resistance and their utilization to improve patient risk stratification and treatment personalization are addressed. Finally, we discuss some of the current treatments and future strategies to circumvent the development of cisplatin resistance.

Keywords: DNA damage response; anticancer drugs; cisplatin; cisplatin resistance.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / therapeutic use*
  • Antineoplastic Agents / toxicity
  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / metabolism
  • Cisplatin / therapeutic use*
  • Cisplatin / toxicity
  • DNA Damage*
  • DNA Repair*
  • Drug Resistance, Neoplasm*
  • Humans
  • Neoplasms / drug therapy
  • Neoplasms / genetics*
  • Neoplasms / metabolism

Substances

  • Antineoplastic Agents
  • Biomarkers, Tumor
  • Cisplatin