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乳腺癌中的 DNA 修复途径:从机制到临床应用。

DNA repair pathways in breast cancer: from mechanisms to clinical applications.

机构信息

Institute of Biomedical Sciences, Shanxi University, Taiyuan, 030006, China.

出版信息

Breast Cancer Res Treat. 2023 Aug;200(3):305-321. doi: 10.1007/s10549-023-06995-z. Epub 2023 Jun 8.

DOI:10.1007/s10549-023-06995-z
PMID:37289340
Abstract

BACKGROUND

Breast cancer (BC) is a complex disease with various subtypes and genetic alterations that impact DNA repair pathways. Understanding these pathways is essential for developing effective treatments and improving patient outcomes.

AREA COVERED

This study investigates the significance of DNA repair pathways in breast cancer, specifically focusing on various pathways such as nucleotide excision repair, base excision repair, mismatch repair, homologous recombination repair, non-homologous end joining, fanconi anemia pathway, translesion synthesis, direct repair, and DNA damage tolerance. The study also examines the role of these pathways in breast cancer resistance and explores their potential as targets for cancer treatment.

CONCLUSION

Recent advances in targeted therapies have shown promise in exploiting DNA repair pathways for BC treatment. However, much research is needed to improve the efficacy of these therapies and identify new targets. Additionally, personalized treatments that target specific DNA repair pathways based on tumor subtype or genetic profile are being developed. Advances in genomics and imaging technologies can potentially improve patient stratification and identify biomarkers of treatment response. However, many challenges remain, including toxicity, resistance, and the need for more personalized treatments. Continued research and development in this field could significantly improve BC treatment.

摘要

背景

乳腺癌(BC)是一种复杂的疾病,具有多种亚型和遗传改变,这些改变会影响 DNA 修复途径。了解这些途径对于开发有效的治疗方法和改善患者的预后至关重要。

涵盖领域

本研究探讨了 DNA 修复途径在乳腺癌中的意义,特别是关注核苷酸切除修复、碱基切除修复、错配修复、同源重组修复、非同源末端连接、范可尼贫血途径、跨损伤合成、直接修复和 DNA 损伤耐受等各种途径。本研究还研究了这些途径在乳腺癌耐药中的作用,并探讨了它们作为癌症治疗靶点的潜力。

结论

靶向治疗的最新进展表明,利用 DNA 修复途径治疗 BC 具有一定的前景。然而,为了提高这些疗法的疗效并确定新的靶点,还需要进行大量的研究。此外,正在开发基于肿瘤亚型或遗传特征针对特定 DNA 修复途径的个体化治疗方法。基因组学和成像技术的进步可能会提高患者的分层能力,并识别治疗反应的生物标志物。然而,仍存在许多挑战,包括毒性、耐药性以及对更个体化治疗的需求。该领域的持续研究和开发可能会显著改善 BC 的治疗效果。

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Coordinated activation of c-Src and FOXM1 drives tumor cell proliferation and breast cancer progression.c-Src 和 FOXM1 的协调激活驱动肿瘤细胞增殖和乳腺癌进展。
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Relationship between polymorphisms in homologous recombination repair genes RAD51 G172T、XRCC2 & XRCC3 and risk of breast cancer: A meta-analysis.
利用复制应激实现MYC驱动癌症中的合成致死效应。
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DNA damage repair-related methylated genes RRM2 and GAPDH are prognostic biomarkers associated with immunotherapy for lung adenocarcinoma.DNA损伤修复相关甲基化基因RRM2和GAPDH是与肺腺癌免疫治疗相关的预后生物标志物。
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Role of MRE11 in DNA damage repair pathway dynamics and its diagnostic and prognostic significance in hereditary breast and ovarian cancer.MRE11在DNA损伤修复途径动态变化中的作用及其在遗传性乳腺癌和卵巢癌中的诊断和预后意义。
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Somatic gene mutations involved in DNA damage response/Fanconi anemia signaling are tissue- and cell-type specific in human solid tumors.参与DNA损伤反应/范可尼贫血信号传导的体细胞基因突变在人类实体瘤中具有组织和细胞类型特异性。
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