Department of Biology, Faculty of Science, Ferdowsi University of Mashhad, Mashhad, Iran.
Department of Epidemiology, School of Public Health, Shahroud University of Medical Sciences, Shahroud, Iran.
Iran J Allergy Asthma Immunol. 2020 Apr 16;19(2):105-116. doi: 10.18502/ijaai.v19i2.2756.
Despite the importance of CD44 and CD133 in various cancers, the clinicopathological and prognostic values of these biomarkers in esophageal cancer remain debated. Hence, in this study, we did a meta-analysis to explore the correlation between overexpression of these markers and some clinicopathological features and their influence on the survival of esophageal cancer patients. A search in PubMed and Web of Science (among all articles published up to January 16, 2018) was done using the following keywords: esophageal cancer, CD44, CD133, prominin-1, AC133. Suitable studies, that were selected based on the criteria listed in the Materials and Methods section, were chosen and hazard ratios with 95% confidence intervals were estimated if available. Heterogeneity and sensitivity were also analyzed. Furthermore, publication bias was assessed using funnel plots, Egger, and Begg tests. The study included 1346 patients from 13 related studies. The median rates of marker expressions by immunohistochemistry were 35.7% (30%-76.6%) from 9 studies for CD44 and 31.9% (21%-44.2%) from 5 studies for CD133. The accumulative 5-year overall survival rates of CD44-positive and CD133-positive were 1.59% (1.22-2.06) and 1.27% (0.93-1.73), respectively. Meta-analysis showed that CD44 expression had a significant correlation with 5-year overall survival. CD44 overexpression showed a correlation with some clinicopathological features such as lymph node metastasis, vascular invasion, and recurrence of the disease, while it was not the case for coexpression of CD44 and CD133. In conclusion, CD44 overexpression was associated with a 5-year overall survival rate and thus this biomarker can be a suitable prognostic tool in esophageal cancer.
尽管 CD44 和 CD133 在各种癌症中具有重要作用,但这些生物标志物在食管癌中的临床病理和预后价值仍存在争议。因此,本研究通过荟萃分析来探讨这些标志物的过度表达与某些临床病理特征之间的相关性,以及它们对食管癌患者生存的影响。我们在 PubMed 和 Web of Science(截至 2018 年 1 月 16 日发布的所有文章)中使用以下关键词进行了搜索:食管癌、CD44、CD133、prominin-1、AC133。选择符合纳入标准的研究,根据材料和方法部分列出的标准进行选择,并在有可用数据的情况下计算风险比及其 95%置信区间。还分析了异质性和敏感性。此外,使用漏斗图、Egger 和 Begg 检验评估发表偏倚。该研究纳入了 13 项相关研究的 1346 名患者。9 项研究中 CD44 免疫组化的标志物表达中位数为 35.7%(30%-76.6%),5 项研究中 CD133 的标志物表达中位数为 31.9%(21%-44.2%)。CD44 阳性和 CD133 阳性的累积 5 年总生存率分别为 1.59%(1.22-2.06)和 1.27%(0.93-1.73)。荟萃分析表明,CD44 表达与 5 年总生存率显著相关。CD44 过表达与淋巴结转移、血管侵犯和疾病复发等一些临床病理特征相关,而 CD44 和 CD133 的共表达则不然。总之,CD44 过表达与 5 年总生存率相关,因此该生物标志物可作为食管癌的一种合适的预后工具。