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8
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9
High expression of KIF20A in bladder cancer as a potential prognostic target for poor survival of renal cell carcinoma.膀胱癌中 KIF20A 的高表达作为肾细胞癌不良生存的潜在预后靶点。
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[RAD51AP1在肿瘤进展和耐药性中的研究进展]

[Research Advances of RAD51AP1 in Tumor Progression and Drug Resistance].

作者信息

Liu Renwang, Li Mingbiao, Hu Zixuan, Song Zuoqing, Chen Jun

机构信息

Department of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin 300052, China.

Tianjin Key Laboratory of Lung Cancer
Metastasis and Tumor Microenvironment, Tianjin Lung Cancer Institute, Tianjin 300052, China.

出版信息

Zhongguo Fei Ai Za Zhi. 2023 Sep 20;26(9):701-708. doi: 10.3779/j.issn.1009-3419.2023.102.34.

DOI:10.3779/j.issn.1009-3419.2023.102.34
PMID:37985156
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10600754/
Abstract

The genomic instability may lead to an initiation of cancer in many organisms. Homologous recombination repair (HRR) is vital in maintaining cellular genomic stability. RAD51 associated protein 1 (RAD51AP1), which plays a crucial role in HRR and primarily participates in forming D-loop, was reported as an essential protein for maintaining cellular genomic stability. However, recent studies showed that RAD51AP1 was significantly overexpressed in various cancer types and correlated with poor prognosis. These results suggested that RAD51AP1 may play a significant pro-cancer effect in multiple cancers. The underlying mechanism is still unclear. Cancer stemness-maintaining effects of RAD51AP1 might be considered as the most reliable mechanism. Meanwhile, RAD51AP1 also promoted resistance to radiation therapy and chemotherapy in many cancers. Thus, researches focused on RAD51AP1, and its regulatory molecules may provide new targets for overcoming cancer progression and treatment resistance. Here, we reviewed the latest research on RAD51AP1 in cancers and summarized its differential expression and prognostic implications. In this review, we also outlined the potential mechanisms of its pro-cancer and drug resistance-promoting effects to provide several potential directions for further research.
.

摘要

基因组不稳定可能在许多生物体中引发癌症。同源重组修复(HRR)对于维持细胞基因组稳定性至关重要。据报道,RAD51相关蛋白1(RAD51AP1)在HRR中起关键作用,主要参与D环的形成,是维持细胞基因组稳定性的必需蛋白。然而,最近的研究表明,RAD51AP1在多种癌症类型中显著过表达,且与预后不良相关。这些结果表明,RAD51AP1可能在多种癌症中发挥显著的促癌作用。其潜在机制仍不清楚。RAD51AP1维持癌症干性的作用可能被认为是最可靠的机制。同时,RAD51AP1在许多癌症中还促进对放疗和化疗的抗性。因此,针对RAD51AP1及其调控分子的研究可能为克服癌症进展和治疗抗性提供新的靶点。在此,我们综述了RAD51AP1在癌症方面的最新研究,并总结了其差异表达及预后意义。在本综述中,我们还概述了其促癌和促进耐药作用的潜在机制,为进一步研究提供几个潜在方向。