Department of Orthopaedics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Department of Orthopaedic Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
BMC Cancer. 2018 Jul 13;18(1):736. doi: 10.1186/s12885-018-4655-4.
MLKL is the most important executor of necroptosis pathway. Recent studies have demonstrated that MLKL could serve as a potential prognostic biomarker for cancer patients. However, most studies reported so far are limited in discrete outcome and sample size.
We systematically searched PubMed, Embase, Web of Science and CNKI to obtain all relevant articles about the prognostic value of abnormally expressed MLKL in patients with any type of tumor. Odds ratios or hazards ratios (HRs) with corresponding 95% confidence intervals (CIs) were pooled to estimate the association between MLKL expression and clinicopathological characteristics or survival of cancer patients.
A total of 6 eligible studies with 613 cancer patients were enrolled in our meta-analysis. Our results demonstrated that decreased expression level of MLKL was significantly associated with poor overall survival (OS) (pooled HR 0.26, 95%CI 0.17-0.40, high/low) and event-free survival (EFS) (pooled HR 0.45, 95%CI 0.23-0.87, high/low) in cancer patients. Furthermore, subgroup analysis divided by type of cancer, sample size, follow-up time and Newcastle-Ottawa Scale (NOS) score showed consistent prognostic value. In addition, our analysis revealed that decreased expression level of MLKL was significantly associated with advanced tumor stage, more lymph node metastasis and older age.
In conclusion, our meta-analysis suggested that decreased MLKL expression might be a convinced unfavorable prognostic factor that could help the clinical decision-making process.
MLKL 是坏死性凋亡途径的最重要执行者。最近的研究表明,MLKL 可以作为癌症患者的潜在预后生物标志物。然而,到目前为止,大多数研究报告的结果仅限于离散的结局和样本量。
我们系统地检索了 PubMed、Embase、Web of Science 和中国知网,以获取所有关于任何类型肿瘤中异常表达 MLKL 的预后价值的相关文章。使用比值比或风险比(HRs)及其相应的 95%置信区间(CIs)来评估 MLKL 表达与癌症患者的临床病理特征或生存之间的关系。
共有 6 项符合条件的研究纳入了 613 名癌症患者,我们的荟萃分析结果表明,MLKL 表达水平降低与总生存期(OS)(合并 HR 0.26,95%CI 0.17-0.40,高/低)和无事件生存期(EFS)(合并 HR 0.45,95%CI 0.23-0.87,高/低)显著相关。进一步按癌症类型、样本量、随访时间和纽卡斯尔-渥太华量表(NOS)评分进行亚组分析,均显示出一致的预后价值。此外,我们的分析表明,MLKL 表达水平降低与肿瘤分期较晚、淋巴结转移较多和年龄较大显著相关。
总之,我们的荟萃分析表明,MLKL 表达降低可能是一个令人信服的不利预后因素,可以帮助临床决策过程。