血清胸苷激酶1浓度对胃癌进展风险评估的益处:系统回顾和荟萃分析

Ailian Hei, Hongbo Ma, Maogang Li, Jin Li, Ji Zhou, E. He, S. Skog
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引用次数: 0

摘要

背景:人胸苷激酶1 (Human Thymidine kinase 1, hTK1)是参与细胞周期s期DNA合成和细胞增殖上调的关键酶,是评估肿瘤血清和组织中肿瘤增殖率的可靠肿瘤增殖生物标志物。本meta分析旨在探讨基于htk1 - igy多克隆抗体的血清TK1浓度(STK1p)是否可用于胃癌进展风险评估及胃癌治疗效果评估。1.2. 方法:从2008年5月1日至2021年11月30日的PubMed、Embase、中国国家知识基础设施、万方、重庆VIP中文科技期刊库和中国生物医学文献库等电子数据库中检索相关研究。采用改良的纽卡斯尔-渥太华量表评价研究质量。使用Review manager和STATA软件评估加权平均差(MD)、敏感性分析和发表偏倚的汇总估计。结果:27项研究包括1909例GCs和1229例肿瘤(浅表性胃炎、慢性胃炎、萎缩性胃溃疡和胃溃疡)和2260例无肿瘤患者。结果显示,STK1p水平在无肿瘤组<浅表性胃炎组<慢性胃炎组<萎缩性胃炎组<胃溃疡组<胃癌组显著升高(P< 0.006)。术后1个月GCs STK1p值较术前明显下降66%。1.3. 结论:STK1p值有可能作为早期胃肿瘤向胃癌进展的早期风险预警指标,并可作为监测手术反应的有用指标。1.4. 核心提示:尽管在诊断和治疗方面有所改进,但大量GCs的长期生存率仍然令人沮丧。因此,探索血清生物标志物对早期预测胃肿瘤发展为胃癌的风险具有重要意义。在这项荟萃分析中,作为预后生物标志物的STK1p被调查显示,与不同的肿瘤和无肿瘤患者相比,GCs中的STK1p显著升高,并且在手术后一个月显著降低。说明STK1p作为肿瘤增殖血清生物标志物,不仅可用于胃癌患者胃肿瘤早期危险进展和治疗效果评价,还可用于临床其他多种肿瘤类型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Benefit of Serum Thymidine Kinase 1 Concentration for Risk Assessment from Gastric Neoplasms Progression to Carcinomas: A Systematic Review and Meta-analysis
Background: Human Thymidine kinase 1 (hTK1), a key enzyme involved in the DNA synthesis during S-phase of the cell cycle and upregulation of cell proliferation, thus it is reliable tumor proliferating biomarker for assessment of tumor proliferation rate in serum and in tissue in oncology. This meta-analysis is investigation whether the serum TK1 concentration(STK1p)based on hTK1-IgY-polyclonal-antibody can provide a benefit for risk assessment from gastric neoplasm progression to gastric carcinoma (GC) as well as for evaluation of treatment effect in GC. 1.2. Methods: Relevant studies were identified from the following electronic databases: PubMed, Embase, Chinese National Knowledge Infrastructure, Wanfang, the Chongqing VIP Chinese Science and Technology Periodical Database and Chinese Biomedical Literature Database from May 1, 2008, until November 30, 2021. Study quality was evaluated by the modified Newcastle-Ottawa Scale. Pooled estimates of weighted mean difference (MD), sensitivity analyses and publication bias were evaluated using Review manager and STATA software. RESULTS: Twenty-seven studies included to 1,909 GCs and 1,229 neoplasms (superficial gastritis, chronic gastritis, atrophic and gastric ulcers) and 2,260 tumor-frees. The results showed that STK1p levels increased significantly in the following manner (P<.0.006): tumor-free < superficial gastritis < chronic gastritis < atrophic gastritis < gastric ulcer < GC. The STK1p value of the GCs one-month-post-surgery decline significantly by 66% compared to pre-surgery. 1.3. Conclusion: STK1p value has the potential to be an early risk warning indicator for early gastric neoplasms progression to GCs and to be a helpful index for monitoring the response to surgery. 1.4. Core Tip: In spite of improvements in diagnosis and treatment the long-term survival rate for a large number of GCs is still dismal. Hence, it is important to explore serum biomarkers for early prediction of risk gastric neoplasms into GCs. In this meta-analysis, the STK1p as a prognostic biomarker was investigated showed significantly higher in GCs compere to different neoplasm and tumor-free people and was significantly reduced one-month post-surgery. It demonstrates that STK1p as tumor proliferating serum-biomarker, can be not only used for early risk gastric neoplasm progression and evaluation of treatment effect in GC patients, but also for a variety of other tumor types in clinical setting.
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