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胃癌原发灶及淋巴结转移组织中肿瘤干细胞标志物 ALDH1、CD44 和 CD133 的表达。

Expression of cancer stem cell markers ALDH1, CD44 and CD133 in primary tumor and lymph node metastasis of gastric cancer.

机构信息

Department of Molecular Pathology, Hiroshima University Graduate School of Biomedical Sciences, Hiroshima, Japan.

出版信息

Pathol Int. 2012 Feb;62(2):112-9. doi: 10.1111/j.1440-1827.2011.02760.x. Epub 2011 Nov 30.

DOI:10.1111/j.1440-1827.2011.02760.x
PMID:22243781
Abstract

Gastric cancer (GC) is one of the most common malignancies worldwide. Recently, cancer stem cells (CSCs) in tumors were found to possess the ability to sustain tumor self-renewal, initiate tumor progression, and possibly also contribute to cancer metastasis. We immunohistochemically examined expression and distribution of representative CSC markers ALDH1, CD44, and CD133 in primary tumors and lymph node metastasis of GC. Among 190 GC primary tumors, 104 (55%) were positive for ALDH1, 117 (62%) were positive for CD44, and 18 (9%) were positive for CD133. Expression of these three CSC markers was significantly associated with advanced clinicopathologic factors. Patients with CD44- and CD133-positive GC had a poorer survival rate than patients with CD44- and CD133-negative GC (CD44: P < 0.001, CD133: P= 0.006). Univariate and multivariate Cox proportional hazards analysis revealed tumor node metastasis stage, CD44 expression, and CD133 expression to be independent predictors of survival in patients with GC. Comparison of CSC markers in primary and metastatic sites showed ALDH1 positivity to be significantly higher in diffuse-type lymph node metastasis than in the primary tumor (P < 0.001). These results indicate that these CSC markers are important in tumor invasion and metastasis and may be good markers indicating long-term survival in patients with GC.

摘要

胃癌(GC)是全球最常见的恶性肿瘤之一。最近,研究发现肿瘤中的癌症干细胞(CSC)具有维持肿瘤自我更新、启动肿瘤进展以及可能促进癌症转移的能力。我们免疫组化检测了 GC 原发肿瘤和淋巴结转移中代表性 CSC 标志物 ALDH1、CD44 和 CD133 的表达和分布。在 190 例 GC 原发肿瘤中,有 104 例(55%)ALDH1 阳性,117 例(62%)CD44 阳性,18 例(9%)CD133 阳性。这些 CSC 标志物的表达与晚期临床病理因素显著相关。CD44 和 CD133 阳性 GC 患者的生存率低于 CD44 和 CD133 阴性 GC 患者(CD44:P<0.001,CD133:P=0.006)。单因素和多因素 Cox 比例风险分析显示,肿瘤淋巴结转移分期、CD44 表达和 CD133 表达是 GC 患者生存的独立预测因素。原发和转移部位 CSC 标志物的比较显示,弥漫型淋巴结转移中 ALDH1 的阳性率明显高于原发肿瘤(P<0.001)。这些结果表明,这些 CSC 标志物在肿瘤侵袭和转移中很重要,可能是 GC 患者长期生存的良好标志物。

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