Peng Qiliang, Shen Yi, Zhao Peifeng, Cheng Ming, Wu Yongyou, Zhu Yaqun
Department of Radiotherapy & Oncology, The Second Affiliated Hospital of Soochow University, San Xiang Road No. 1055, Suzhou, 215004 Jiangsu China.
Institute of Radiotherapy & Oncology, Soochow University, Suzhou, China.
Cancer Cell Int. 2020 Jun 22;20:260. doi: 10.1186/s12935-020-01350-4. eCollection 2020.
Recent studies have demonstrated that the kallikrein and kallikrein-related peptidases (KLKs) exhibit aberrant expression in patients with colorectal cancer (CRC) and might be considered as potential prognostic biomarkers of CRC. However, inconsistent findings have been reported, which promote us to summarize the global prognostic roles of KLKs for survival in CRC patients.
Eligible published studies were identified by searching electronic databases with several search strategies. The patients' baseline characteristics and survival results were extracted from enrolled studies and pooled as combined hazard ratio (HR) with 95% confidence interval (95% CI) to estimate the effect size.
A total of 25 and 22 eligible studies were included in the meta-analysis to evaluate the prognostic roles of KLKs on overall survival (OS) and disease-free survival (DFS), respectively. KLKs overexpression was significantly associated with worse OS (pooled HR = 1.43, 95% CI 1.27-1.60, P < 0.001) and short DFS (pooled HR = 1.35, 95% CI 1.21-1.51, P < 0.001). Importantly, subgroup and meta-regression analyses revealed the survival differences among different races and detection methods of KLKs. Furthermore, several specific members of KLKs were identified to be more significantly related to worse OS and DFS compared with other members.
The present study demonstrated that KLKs may have the potential to serve as promising biomarkers to monitor CRC prognosis and progression. The promising results concerning the utility of KLKs in clinical practice encourage the further investigation of their clinical utility applicability as tumor markers of CRC.
近期研究表明,激肽释放酶及激肽释放酶相关肽酶(KLKs)在结直肠癌(CRC)患者中表达异常,可能被视为CRC潜在的预后生物标志物。然而,已有报道结果不一致,这促使我们总结KLKs对CRC患者生存的整体预后作用。
通过多种检索策略搜索电子数据库,以确定符合条件的已发表研究。从纳入研究中提取患者的基线特征和生存结果,并汇总为合并风险比(HR)及95%置信区间(95%CI),以估计效应大小。
荟萃分析共纳入25项和22项符合条件的研究,分别评估KLKs对总生存期(OS)和无病生存期(DFS)的预后作用。KLKs过表达与较差的OS(合并HR = 1.43,95%CI 1.27 - 1.60,P < 0.001)和较短的DFS(合并HR = 1.35,95%CI 1.21 - 1.51,P < 0.001)显著相关。重要的是,亚组和荟萃回归分析揭示了不同种族和KLKs检测方法之间的生存差异。此外,与其他成员相比,已确定KLKs的几个特定成员与较差的OS和DFS更显著相关。
本研究表明,KLKs可能有潜力作为监测CRC预后和进展的有前景的生物标志物。关于KLKs在临床实践中的应用的有前景结果鼓励进一步研究其作为CRC肿瘤标志物的临床应用适用性。