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循环中的端粒酶逆转录酶(TERT)可作为可切除非小细胞肺癌(NSCLC)的新型诊断和预后生物标志物。

Circulating TERT serves as the novel diagnostic and prognostic biomarker for the resectable NSCLC.

作者信息

Chen Guanxuan, Wang Shiwen, Zhang Qianru, Liu Junyan, Zhu Wanqi, Song Xianrang, Song Xingguo

机构信息

Oncology Department, Affiliated Zhongshan Hospital of Dalian University, Dalian, Liaoning, PR China.

Department of Clinical Laboratory, Shandong Cancer Hospital and Institute, Shandong First Medical University, Shandong Academy of Medical Sciences, 440 Ji- Yan Road, Jinan, 250117, Shandong Province, PR China.

出版信息

Cancer Cell Int. 2024 Dec 19;24(1):420. doi: 10.1186/s12935-024-03605-w.

DOI:10.1186/s12935-024-03605-w
PMID:39702287
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11661135/
Abstract

BACKGROUND

Telomerase reverse transcriptase (TERT) is a catalytic subunit of telomerase and required for cancer development. This study aims to reveal its clinical utility for diagnosis and prognosis of resectable NSCLC.

METHODS

TERT was quantitatively evaluated by the enzyme-linked immunosorbent assay (ELISA) from 69 patients before and after the surgery. The prognostic value was evaluated by disease-free survival (DFS) and overall survival (OS).

RESULTS

Circulating TERT in NSCLC patients were significantly higher than that in the healthy group, possessing the AUC of 0.90. Importantly, TERT change between pre- and post- operation was significantly correlated with OS and DFS (p = 0.022, p = 0.046 respectively), acted as the independent prognostic factors for DFS and OS, indicating it can serve as the promising diagnostic and prognostic biomarker for resectable non-small cell lung cancer (NSCLC).

CONCLUSIONS

TERT change between pre- and post- resection can serve as the promising biomarker for prognosis of resectable NSCLC.

摘要

背景

端粒酶逆转录酶(TERT)是端粒酶的催化亚基,是癌症发展所必需的。本研究旨在揭示其在可切除非小细胞肺癌诊断和预后中的临床应用价值。

方法

采用酶联免疫吸附测定(ELISA)对69例患者手术前后的TERT进行定量评估。通过无病生存期(DFS)和总生存期(OS)评估预后价值。

结果

非小细胞肺癌患者的循环TERT显著高于健康组,曲线下面积(AUC)为0.90。重要的是,手术前后TERT的变化与OS和DFS显著相关(分别为p = 0.022,p = 0.046),是DFS和OS的独立预后因素,表明它可作为可切除非小细胞肺癌(NSCLC)有前景的诊断和预后生物标志物。

结论

切除前后TERT的变化可作为可切除非小细胞肺癌预后的有前景的生物标志物。

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Circulating TERT serves as the novel diagnostic and prognostic biomarker for the resectable NSCLC.循环中的端粒酶逆转录酶(TERT)可作为可切除非小细胞肺癌(NSCLC)的新型诊断和预后生物标志物。
Cancer Cell Int. 2024 Dec 19;24(1):420. doi: 10.1186/s12935-024-03605-w.
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本文引用的文献

1
Oligometastatic non-small cell lung cancer: Impact of local and contemporary systemic treatment approaches on clinical outcome.寡转移非小细胞肺癌:局部及当代全身治疗方法对临床结局的影响
Int J Cancer. 2025 Feb 15;156(4):776-787. doi: 10.1002/ijc.35199. Epub 2024 Sep 25.
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Cancer statistics, 2023.癌症统计数据,2023 年。
CA Cancer J Clin. 2023 Jan;73(1):17-48. doi: 10.3322/caac.21763.
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Genetics of human telomere biology disorders.人类端粒生物学障碍的遗传学
Nat Rev Genet. 2023 Feb;24(2):86-108. doi: 10.1038/s41576-022-00527-z. Epub 2022 Sep 23.
4
Perioperative Systemic Therapy for Resectable Non-Small Cell Lung Cancer.可切除非小细胞肺癌的围手术期全身治疗。
J Natl Compr Canc Netw. 2022 Aug;20(8):953-961. doi: 10.6004/jnccn.2022.7021.
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Molecular Biomarkers in Cancer.癌症中的分子生物标志物
Biomolecules. 2022 Jul 23;12(8):1021. doi: 10.3390/biom12081021.
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Practical Management of Oligometastatic Non-Small-Cell Lung Cancer.寡转移非小细胞肺癌的实用管理
J Clin Oncol. 2022 Feb 20;40(6):635-641. doi: 10.1200/JCO.21.01719. Epub 2022 Jan 5.
7
Shorter Leukocyte Telomere Length Is Associated with Worse Survival of Patients with Bladder Cancer and Renal Cell Carcinoma.较短的白细胞端粒长度与膀胱癌和肾细胞癌患者较差的生存率相关。
Cancers (Basel). 2021 Jul 27;13(15):3774. doi: 10.3390/cancers13153774.
8
Human TERT promoter mutations as a prognostic biomarker in glioma.人类端粒酶逆转录酶启动子突变作为胶质瘤的预后生物标志物。
J Cancer Res Clin Oncol. 2021 Apr;147(4):1007-1017. doi: 10.1007/s00432-021-03536-3. Epub 2021 Feb 6.
9
Leukocyte telomere length, cancer incidence and all-cause mortality among Chinese adults: Singapore Chinese Health Study.白细胞端粒长度、中国成年人的癌症发病率和全因死亡率:新加坡华人健康研究。
Int J Cancer. 2021 Jan 15;148(2):352-362. doi: 10.1002/ijc.33211. Epub 2020 Aug 5.
10
TERT-Regulation and Roles in Cancer Formation.TERT 调控与癌症形成中的作用。
Front Immunol. 2020 Nov 19;11:589929. doi: 10.3389/fimmu.2020.589929. eCollection 2020.