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Modulating the DNA Damage Response to Improve Treatment Response in Cervical Cancer
Abstract
Cervical cancer is the fourth most common cause of cancer-related death in women worldwide and new therapeutic approaches are needed to improve clinical outcomes for this group of patients. Current treatment protocols for locally advanced and metastatic disease consist of ionising radiation and chemotherapy. Chemoradiation induces cytotoxic levels of DNA double-strand breaks, which activates programmed cell death via the DNA damage response (DDR). Cervical cancers are unique given an almost exclusive association with human papillomavirus (HPV) infection; a potent manipulator of the DDR, with the potential to alter tumour sensitivity to DNA-damaging agents and influence treatment response. This review highlights the wide range of therapeutic strategies in development that have the potential to modulate DDR and sensitise cervical tumours to DNA-damaging agents in the context of HPV oncogenesis.
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“HPV-positive CC is recognized as more sensitive to DNA-damaging therapy compared to HPV-negative counterparts [30].”
From Combining Mitomycin C with inhibition of BAD phosphorylation enhances apoptotic cell death in advanced cervical cancer (2024) · cites this paper as [30]
Citations
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Reaper, P. M., Griffiths, M. R., Long, J. M., Charrier, J.-D., MacCormick, S., Charlton, P. A., Golec, J. M. C., & Pollard, J. R. (2011) · Nature Chemical Biology · doi:10.1038/nchembio.573 · Cited by 633
Cisplatin Resistance Associated with PARP Hyperactivation
Michels, J., Vitale, I., Galluzzi, L., Adam, J., Olaussen, K. A., Kepp, O., Senovilla, L., Talhaoui, I., Guegan, J., Enot, D. P., et al. (2013) · Cancer Research · doi:10.1158/0008-5472.can-12-3000 · Cited by 176
Hsp90: A New Player in DNA Repair?
Pennisi, R., Ascenzi, P., & Di Masi, A. (2015) · Biomolecules · doi:10.3390/biom5042589 · Cited by 112
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Cited by
Sorted by citations
Wang, L., Zhang, X., Chen, S., Ye, Q., Basappa, B., Zhu, T., Lobie, P. E., & Pandey, V. (2024) · Translational Oncology · doi:10.1016/j.tranon.2024.102103 · Cited by 8
“HPV-positive CC is recognized as more sensitive to DNA-damaging therapy compared to HPV-negative counterparts [30].”
Metadata
- Authors
- Cossar, L. H., Schache, A. G., Risk, J. M., Sacco, J. J., Jones, N. J., & Lord, R.
- Affiliations
- University of Liverpool (GB)
- Clatterbridge Cancer Centre NHS Foundation Trust (GB)
- Corresponding author
- Cossar, L.H.
- Venue
- Clinical Oncology
- Publisher
- Elsevier BV
- Published
- 2017-09
- Volume
- 29
- Issue
- 9
- Pages
- 626-634
- ISSN
- 0936-6555 (ISSN-L)
- OpenAlex
- W2599052812
- Cited by
- 12
- References
- 3
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 1 · 2022: 1 · 2021: 2 · 2019: 2 · 2018: 3 · 2017: 1
- FWCI
- 0.22
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Clinical Oncology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Clatterbridge Cancer Centre
- University of Liverpool
- Topics
- Health Sciences › Medicine › Epidemiology › Cervical Cancer and HPV Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Health Sciences › Medicine › Obstetrics and Gynecology › Endometrial and Cervical Cancer Treatments
- Keywords
- cervical cancer, DNA damage response, human papillomavirus, chemoradiotherapy, DNA double-strand breaks, radiosensitization, chemosensitization, HPV oncogenesis, treatment response
- MeSH terms
- Uterine Cervical Neoplasms, DNA Damage, Female, Humans, Papillomavirus Infections
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