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TRIP13 在人类癌症发展中的作用。

Role of TRIP13 in human cancer development.

机构信息

Institute of Urology, Lanzhou University Second Hospital, NO.82 Linxia Road, Chengguan District Lanzhou, Lanzhou, Gansu Province, 730030, PR China.

Gansu Province Clinical Research Center for urinary system disease, Lanzhou, Gansu Province, 730030, PR China.

出版信息

Mol Biol Rep. 2024 Oct 22;51(1):1088. doi: 10.1007/s11033-024-10012-x.

DOI:10.1007/s11033-024-10012-x
PMID:39436503
Abstract

As an AAA + ATPase, thyroid hormone receptor interacting protein 13 (TRIP13) primarily functions in DNA double-strand break repair, chromosome recombination, and cell cycle checkpoint regulation; aberrant expression of TRIP13 can result in chromosomal instability (CIN). According to recent research, TRIP13 is aberrantly expressed in a variety of cancers, and a patient's poor prognosis and tumor stage are strongly correlated with high expression of TRIP13. Tumor cell and subcutaneous xenograft growth can be markedly inhibited by TRIP13 knockdown or TRIP13 inhibitor administration. In the initiation and advancement of human malignancies, TRIP13 seems to function as an oncogene. Based on available data, TRIP13 may function as a biological target and biomarker for cancer. The creation of inhibitors that specifically target TRIP13 may present novel approaches to treating cancer.

摘要

作为一个 AAA+ATPase,甲状腺激素受体相互作用蛋白 13(TRIP13)主要在 DNA 双链断裂修复、染色体重组和细胞周期检查点调节中发挥作用;TRIP13 的异常表达会导致染色体不稳定(CIN)。最近的研究表明,TRIP13 在多种癌症中异常表达,患者的预后不良和肿瘤分期与 TRIP13 的高表达强烈相关。TRIP13 的敲低或 TRIP13 抑制剂的给药可以显著抑制肿瘤细胞和皮下异种移植的生长。在人类恶性肿瘤的发生和进展中,TRIP13 似乎作为一种癌基因发挥作用。基于现有数据,TRIP13 可能是癌症的生物靶标和生物标志物。开发特异性靶向 TRIP13 的抑制剂可能为癌症治疗提供新的方法。

相似文献

1
Role of TRIP13 in human cancer development.TRIP13 在人类癌症发展中的作用。
Mol Biol Rep. 2024 Oct 22;51(1):1088. doi: 10.1007/s11033-024-10012-x.
2
Thyroid hormone receptor interactor 13 (TRIP13) overexpression associated with tumor progression and poor prognosis in lung adenocarcinoma.甲状腺激素受体相互作用蛋白 13(TRIP13)过表达与肺腺癌的肿瘤进展和不良预后相关。
Biochem Biophys Res Commun. 2018 May 15;499(3):416-424. doi: 10.1016/j.bbrc.2018.03.129. Epub 2018 Mar 30.
3
TRIP13 impairs mitotic checkpoint surveillance and is associated with poor prognosis in multiple myeloma.TRIP13损害有丝分裂检查点监测,与多发性骨髓瘤的不良预后相关。
Oncotarget. 2017 Apr 18;8(16):26718-26731. doi: 10.18632/oncotarget.14957.
4
Thyroid Receptor-Interacting Protein 13 is Correlated with Progression and Poor Prognosis in Bladder Cancer.甲状腺受体相互作用蛋白 13 与膀胱癌的进展和不良预后相关。
Med Sci Monit. 2019 Sep 5;25:6660-6668. doi: 10.12659/MSM.917112.
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Increased expression of TRIP13 drives the tumorigenesis of bladder cancer in association with the EGFR signaling pathway.TRIP13 的表达增加与 EGFR 信号通路一起驱动膀胱癌的肿瘤发生。
Int J Biol Sci. 2019 Jun 2;15(7):1488-1499. doi: 10.7150/ijbs.32718. eCollection 2019.
6
TRIP13 promotes metastasis of colorectal cancer regardless of p53 and microsatellite instability status.TRIP13 促进结直肠癌的转移,而与 p53 和微卫星不稳定性状态无关。
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Elevated TRIP13 drives the AKT/mTOR pathway to induce the progression of hepatocellular carcinoma via interacting with ACTN4.TRIP13 升高通过与 ACTN4 相互作用驱动 AKT/mTOR 通路诱导肝细胞癌的进展。
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Repeated ionizing radiation exposure induces TRIP13 expression, conferring radioresistance in lung cancer cells.反复暴露于电离辐射会诱导TRIP13表达,赋予肺癌细胞放射抗性。
Sci Rep. 2025 Jan 6;15(1):985. doi: 10.1038/s41598-024-84592-w.
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Upregulation of TRIP13 promotes the malignant progression of lung cancer via the EMT pathway.TRIP13 的上调通过 EMT 通路促进肺癌的恶性进展。
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10
TRIP13 - a potential drug target in cancer pharmacotherapy.TRIP13 - 癌症药物治疗中的一个潜在药物靶点。
Bioorg Chem. 2024 Oct;151:107650. doi: 10.1016/j.bioorg.2024.107650. Epub 2024 Jul 18.

本文引用的文献

1
RIOK1 synergizes with TRIP13 by regulating the E2F-Rb signaling pathway to promote the proliferation of esophageal cancer cells.RIOK1通过调节E2F-Rb信号通路与TRIP13协同作用,促进食管癌细胞增殖。
Genes Dis. 2023 Jun 24;11(3):100990. doi: 10.1016/j.gendis.2023.04.024. eCollection 2024 May.
2
Germline specific genes increase DNA double-strand break repair and radioresistance in lung adenocarcinoma cells.胚系特异性基因增加肺腺癌细胞的 DNA 双链断裂修复和放射抗性。
Cell Death Dis. 2024 Jan 12;15(1):38. doi: 10.1038/s41419-024-06433-y.
3
Design and synthesis of cantharidin derivative DCZ5418 as a TRIP13 inhibitor with anti-multiple myeloma activity in vitro and in vivo.
设计并合成斑蝥素衍生物 DCZ5418 作为一种 TRIP13 抑制剂,具有体外和体内抗多发性骨髓瘤活性。
Bioorg Med Chem Lett. 2024 Jan 15;98:129590. doi: 10.1016/j.bmcl.2023.129590. Epub 2023 Dec 12.
4
An integrated computational biology approach defines the crucial role of TRIP13 in pancreatic cancer.一种综合计算生物学方法确定了TRIP13在胰腺癌中的关键作用。
Comput Struct Biotechnol J. 2023 Nov 17;21:5765-5775. doi: 10.1016/j.csbj.2023.11.029. eCollection 2023.
5
TI17, a novel compound, exerts anti-MM activity by impairing Trip13 function of DSBs repair and enhancing DNA damage.TI17 是一种新型化合物,通过损害 DSBs 修复的 Trip13 功能和增强 DNA 损伤来发挥抗多发性骨髓瘤活性。
Cancer Med. 2023 Dec;12(23):21321-21334. doi: 10.1002/cam4.6706. Epub 2023 Nov 9.
6
Ribosomal protein S3 mediates drug resistance of proteasome inhibitor: potential therapeutic application in multiple myeloma.核糖体蛋白 S3 介导蛋白酶体抑制剂耐药性:多发性骨髓瘤潜在的治疗应用。
Haematologica. 2024 Apr 1;109(4):1206-1219. doi: 10.3324/haematol.2023.282789.
7
Aberrant activation of TRIP13-EZH2 signaling axis promotes stemness and therapy resistance in multiple myeloma.TRIP13-EZH2信号轴的异常激活促进多发性骨髓瘤的干性和治疗抗性。
Leukemia. 2023 Jul;37(7):1576-1579. doi: 10.1038/s41375-023-01925-w. Epub 2023 May 8.
8
Alternative CDC20 translational isoforms tune mitotic arrest duration.替代的 CDC20 翻译后异构体调节有丝分裂阻滞持续时间。
Nature. 2023 May;617(7959):154-161. doi: 10.1038/s41586-023-05943-7. Epub 2023 Apr 26.
9
Principles and dynamics of spindle assembly checkpoint signalling.纺锤体组装检验点信号转导的原理与动力学。
Nat Rev Mol Cell Biol. 2023 Aug;24(8):543-559. doi: 10.1038/s41580-023-00593-z. Epub 2023 Mar 24.
10
TRIP13/FLNA Complex Promotes Tumor Progression and Is Associated with Unfavorable Outcomes in Melanoma.TRIP13/FLNA复合物促进肿瘤进展并与黑色素瘤的不良预后相关。
J Oncol. 2022 Oct 11;2022:1419179. doi: 10.1155/2022/1419179. eCollection 2022.