» Articles » PMID: 21385444

Differential Contributory Roles of Nucleotide Excision and Homologous Recombination Repair for Enhancing Cisplatin Sensitivity in Human Ovarian Cancer Cells

Overview
Journal Mol Cancer
Publisher Biomed Central
Date 2011 Mar 10
PMID 21385444
Citations 32
Authors
Affiliations
Soon will be listed here.
Abstract

Background: While platinum-based chemotherapeutic agents are widely used to treat various solid tumors, the acquired platinum resistance is a major impediment in their successful treatment. Since enhanced DNA repair capacity is a major factor in conferring cisplatin resistance, targeting of DNA repair pathways is an effective stratagem for overcoming cisplatin resistance. This study was designed to delineate the role of nucleotide excision repair (NER), the principal mechanism for the removal of cisplatin-induced DNA intrastrand crosslinks, in cisplatin resistance and reveal the impact of DNA repair interference on cisplatin sensitivity in human ovarian cancer cells.

Results: We assessed the inherent NER efficiency of multiple matched pairs of cisplatin-sensitive and -resistant ovarian cancer cell lines and their expression of NER-related factors at mRNA and protein levels. Our results showed that only the cisplatin-resistant ovarian cancer cell line PEO4 possessed an increased NER capacity compared to its inherently NER-inefficient parental line PEO1. Several other cisplatin-resistant cell lines, including CP70, CDDP and 2008C13, exhibited a normal and parental cell-comparable NER capacity for removing cisplatin-induced DNA intrastrand cross-links (Pt-GG). Concomitant gene expression analysis revealed discordance in mRNA and protein levels of NER factors in various ovarian cancer cell lines and NER proteins level were unrelated to the cisplatin sensitivity of these cell lines. Although knockdown of NER factors was able to compromise the NER efficiency, it only caused a minimal effect on cisplatin sensitivity. On the contrary, downregulation of BRCA2, a critical protein for homologous recombination repair (HRR), significantly enhanced the efficacy of cisplatin in killing ovarian cancer cell line PEO4.

Conclusion: Our studies indicate that the level of NER factors in ovarian cancer cell lines is neither a determinant of their NER capacity nor of the sensitivity to cisplatin, and suggest that manipulation of the HRR but not the NER factor expression provides an effective strategy for sensitizing cisplatin-resistant tumors to platinating agents.

Citing Articles

Medical Needs and Therapeutic Options for Melanoma Patients Resistant to Anti-PD-1-Directed Immune Checkpoint Inhibition.

Hassel J, Zimmer L, Sickmann T, Eigentler T, Meier F, Mohr P Cancers (Basel). 2023; 15(13).

PMID: 37444558 PMC: 10341224. DOI: 10.3390/cancers15133448.


p53-Dependent Cytoprotective Mechanisms behind Resistance to Chemo-Radiotherapeutic Agents Used in Cancer Treatment.

Krishnaraj J, Yamamoto T, Ohki R Cancers (Basel). 2023; 15(13).

PMID: 37444509 PMC: 10341282. DOI: 10.3390/cancers15133399.


LC-MS/MS Phytochemical Profiling, Antioxidant Activity, and Cytotoxicity of the Ethanolic Extract of L. against Breast Cancer Cell Lines: Computational Studies and Experimental Validation.

Elbouzidi A, Ouassou H, Aherkou M, Kharchoufa L, Meskali N, Baraich A Pharmaceuticals (Basel). 2022; 15(9).

PMID: 36145377 PMC: 9503641. DOI: 10.3390/ph15091156.


Nelfinavir Induces Cytotoxicity towards High-Grade Serous Ovarian Cancer Cells, Involving Induction of the Unfolded Protein Response, Modulation of Protein Synthesis, DNA Damage, Lysosomal Impairment, and Potentiation of Toxicity Caused by....

Subeha M, Goyeneche A, Bustamante P, Lisio M, Burnier J, Telleria C Cancers (Basel). 2022; 14(1).

PMID: 35008264 PMC: 8750028. DOI: 10.3390/cancers14010099.


The DNA damage inducible lncRNA SCAT7 regulates genomic integrity and topoisomerase 1 turnover in lung adenocarcinoma.

Statello L, Ali M, Reischl S, Mahale S, Thankaswamy Kosalai S, Huarte M NAR Cancer. 2021; 3(1):zcab002.

PMID: 34316698 PMC: 8209975. DOI: 10.1093/narcan/zcab002.


References
1.
Ahmad A, Robinson A, Duensing A, van Drunen E, Beverloo H, Weisberg D . ERCC1-XPF endonuclease facilitates DNA double-strand break repair. Mol Cell Biol. 2008; 28(16):5082-92. PMC: 2519706. DOI: 10.1128/MCB.00293-08. View

2.
McHugh P, Spanswick V, Hartley J . Repair of DNA interstrand crosslinks: molecular mechanisms and clinical relevance. Lancet Oncol. 2002; 2(8):483-90. DOI: 10.1016/S1470-2045(01)00454-5. View

3.
Barakat B, Wang Q, Han C, Milum K, Yin D, Zhao Q . Overexpression of DDB2 enhances the sensitivity of human ovarian cancer cells to cisplatin by augmenting cellular apoptosis. Int J Cancer. 2009; 127(4):977-88. PMC: 4180185. DOI: 10.1002/ijc.25112. View

4.
Lehmann A, Stevens S . A rapid procedure for measurement of DNA repair in human fibroblasts and for complementation analysis of xeroderma pigmentosum cells. Mutat Res. 1980; 69(1):177-90. DOI: 10.1016/0027-5107(80)90187-6. View

5.
Koberle B, Roginskaya V, Zima K, Masters J, Wood R . Elevation of XPA protein level in testis tumor cells without increasing resistance to cisplatin or UV radiation. Mol Carcinog. 2008; 47(8):580-6. DOI: 10.1002/mc.20418. View