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Targeting DNA Damage Response and Repair to Enhance Therapeutic Index in Cisplatin-Based Cancer Treatment
- Source :
- International Journal of Molecular Sciences, Vol 22, Iss 8199, p 8199 (2021), International Journal of Molecular Sciences
- Publication Year :
- 2021
- Publisher :
- MDPI AG, 2021.
-
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.
- Subjects :
- 0301 basic medicine
DNA Repair
QH301-705.5
DNA repair
DNA damage
medicine.medical_treatment
cisplatin
Antineoplastic Agents
Context (language use)
Review
DNA damage response
Catalysis
Inorganic Chemistry
03 medical and health sciences
0302 clinical medicine
Therapeutic index
Downregulation and upregulation
Neoplasms
Biomarkers, Tumor
medicine
Animals
Humans
Biology (General)
Physical and Theoretical Chemistry
QD1-999
Molecular Biology
Spectroscopy
Cisplatin
Chemotherapy
business.industry
Organic Chemistry
General Medicine
Computer Science Applications
anticancer drugs
Chemistry
030104 developmental biology
Drug Resistance, Neoplasm
030220 oncology & carcinogenesis
Cancer cell
Cancer research
cisplatin resistance
business
DNA Damage
medicine.drug
Subjects
Details
- ISSN :
- 14220067
- Volume :
- 22
- Database :
- OpenAIRE
- Journal :
- International Journal of Molecular Sciences
- Accession number :
- edsair.doi.dedup.....89b2982f0341ff532e53778da708c209
- Full Text :
- https://doi.org/10.3390/ijms22158199