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使用碱基切除修复基因预测癌症预后

Cancer prognosis using base excision repair genes.

作者信息

Kim Jeongeun, Kang Su-Jin, Jo Nayoon, Kim Seung-Jin, Jang Sunbok

机构信息

College of Pharmacy, Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul 03760, Republic of Korea; Gradutate Program in Innovative Biomaterials Convergence, Ewha Womans University, Seoul 03760, Republic of Korea.

College of Pharmacy, Dongduk Women's University, Seoul 02748, Republic of Korea.

出版信息

Mol Cells. 2025 Feb;48(2):100186. doi: 10.1016/j.mocell.2025.100186. Epub 2025 Jan 17.

DOI:10.1016/j.mocell.2025.100186
PMID:39828060
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11835649/
Abstract

The base excision repair (BER) pathway is a critical mechanism in genomic stability. This review investigates the role of the BER pathway in advanced cancer therapies considering the pivotal role of genetic factors in cancer patient responses and prognosis. BER factors significantly influence genetic instability and cancer prognosis, as well as the effectiveness of chemotherapy and radiation therapy. In various cancers such as breast, colon, lung, and bladder, BER factors have shown potential as critical biological markers for predicting cancer outcomes. This study focuses on the polymorphisms and expression levels of key BER genes, including OGG1, XRCC1, APE1, and Polβ. Our findings demonstrate that the expression levels of BER genes and proteins are closely associated with the risk, progression, treatment response, and prognosis of various cancers. These insights could improve cancer treatments and aid in the development of drugs targeting BER proteins. Ongoing research in this field requires extensive statistical analyses and large-scale prospective studies to effectively utilize BER protein levels. Ultimately, these results suggest that the BER pathway represents a potential target for cancer diagnosis, prognostic prediction, and the development of personalized therapeutic strategies. This paves the way for effective cancer treatment in the future.

摘要

碱基切除修复(BER)途径是基因组稳定性的关键机制。鉴于遗传因素在癌症患者反应和预后中的关键作用,本综述探讨了BER途径在晚期癌症治疗中的作用。BER因子显著影响遗传不稳定性和癌症预后,以及化疗和放疗的有效性。在乳腺癌、结肠癌、肺癌和膀胱癌等多种癌症中,BER因子已显示出作为预测癌症结局的关键生物学标志物的潜力。本研究聚焦于关键BER基因的多态性和表达水平,包括OGG1、XRCC1、APE1和Polβ。我们的研究结果表明,BER基因和蛋白质的表达水平与各种癌症的风险、进展、治疗反应和预后密切相关。这些见解可能会改善癌症治疗,并有助于开发针对BER蛋白的药物。该领域正在进行的研究需要广泛的统计分析和大规模前瞻性研究,以有效利用BER蛋白水平。最终,这些结果表明BER途径是癌症诊断、预后预测和个性化治疗策略开发的潜在靶点。这为未来有效的癌症治疗铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93de/11835649/0f4dc8b36377/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93de/11835649/29e9dd14569b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93de/11835649/aa840b85f503/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93de/11835649/0f4dc8b36377/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93de/11835649/29e9dd14569b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93de/11835649/aa840b85f503/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93de/11835649/0f4dc8b36377/gr3.jpg

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