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The Research Progress on Radiation Resistance of Cervical Cancer

Overview
Journal Front Oncol
Specialty Oncology
Date 2024 Apr 23
PMID 38651153
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Abstract

Cervical carcinoma is the most prevalent gynecology malignant tumor and ranks as the fourth most common cancer worldwide, thus posing a significant threat to the lives and health of women. Advanced and early-stage cervical carcinoma patients with high-risk factors require adjuvant treatment following surgery, with radiotherapy being the primary approach. However, the tolerance of cervical cancer to radiotherapy has become a major obstacle in its treatment. Recent studies have demonstrated that radiation resistance in cervical cancer is closely associated with DNA damage repair pathways, the tumor microenvironment, tumor stem cells, hypoxia, cell cycle arrest, and epigenetic mechanisms, among other factors. The development of tumor radiation resistance involves complex interactions between multiple genes, pathways, and mechanisms, wherein each factor interacts through one or more signaling pathways. This paper provides an overview of research progress on an understanding of the mechanism underlying radiation resistance in cervical cancer.

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References
1.
Wu N, Zhang X, Zhu M, Fang C, Liu X, Wang Y . promoter methylation predicts cervical cancer radiosensitivity and ZNF582 protein overexpression reduces radiosensitivity by cell cycle arrest in S phase. Epigenetics. 2022; 17(12):1786-1799. PMC: 9621039. DOI: 10.1080/15592294.2022.2080995. View

2.
Csibi A, Fendt S, Li C, Poulogiannis G, Choo A, Chapski D . The mTORC1 pathway stimulates glutamine metabolism and cell proliferation by repressing SIRT4. Cell. 2021; 184(8):2256. DOI: 10.1016/j.cell.2021.03.059. View

3.
Jiang W, Ouyang X, Ji Z, Shi W, Wu Y, Yao Q . The PIK3CA-E545K-SIRT4 signaling axis reduces radiosensitivity by promoting glutamine metabolism in cervical cancer. Cancer Lett. 2023; 556:216064. DOI: 10.1016/j.canlet.2023.216064. View

4.
Luo J, Wang W, Tang Y, Zhou D, Gao Y, Zhang Q . mRNA and methylation profiling of radioresistant esophageal cancer cells: the involvement of Sall2 in acquired aggressive phenotypes. J Cancer. 2017; 8(4):646-656. PMC: 5370508. DOI: 10.7150/jca.15652. View

5.
Chen L, Heikkinen L, Wang C, Yang Y, Sun H, Wong G . Trends in the development of miRNA bioinformatics tools. Brief Bioinform. 2018; 20(5):1836-1852. PMC: 7414524. DOI: 10.1093/bib/bby054. View