Department of Surgery, The Sixth People's Hospital Affiliated to Shanghai Jiaotong University, 600 Yishan Road, Shanghai 200233, China.
Med Oncol. 2010 Jun;27(2):304-9. doi: 10.1007/s12032-009-9210-3. Epub 2009 Apr 2.
CD34, cytokeratin (CK) 19, cytokeratin (CK) 20, and Ki67 have been demonstrated to be involved in tumor invasion and angiogenesis. The aim of this study was to analyze the clinicopathological significance of CD34, CK19, CK20, and Ki67 expressions in colorectal cancer (CRC) and to evaluate their involvement in the progression of CRC. CD34, CK19, CK20, and Ki67 expressions were assessed in paraffin-embedded specimens collected from 152 cases of CRC and 30 paired normal colorectal tissues by immunohistochemistry. The relationships between CD34, CK19, CK20, and Ki67 expressions and CRC were evaluated. The association of CD34 and Ki67 protein expressions with the clinicopathological characteristics and the prognosis of CRC were subsequently assessed. CD34, CK19, CK20, and Ki67 expressed highly in CRC tissues relative to normal colorectal tissues. Using immunostaining scoring, a significant correlation of CD34 and Ki67 with the UICC staging and histo-differentiation of CRC was found (P < 0.05), but no such correlation of CK19 and CK20 with the UICC staging and histo-differentiation (P > 0.05). Meanwhile, no relationship of CD34, CK19, CK20, and Ki67 with the location of CRC was found (P > 0.05). Patients with high expressions of CD34 and Ki67 had the lowest survival (P < 0.05). The results suggest that concurrent expression of CD34 and Ki67 may be an important characteristic of CRC which may help in the prediction of CRC progression.
CD34、细胞角蛋白(CK)19、细胞角蛋白(CK)20 和 Ki67 已被证明参与肿瘤浸润和血管生成。本研究旨在分析 CD34、CK19、CK20 和 Ki67 在结直肠癌(CRC)中的表达的临床病理意义,并评估它们在 CRC 进展中的作用。采用免疫组织化学方法检测 152 例 CRC 石蜡包埋标本和 30 对配对正常结直肠组织中 CD34、CK19、CK20 和 Ki67 的表达。评估 CD34、CK19、CK20 和 Ki67 表达与 CRC 的关系。随后评估 CD34 和 Ki67 蛋白表达与 CRC 的临床病理特征和预后的关系。CD34、CK19、CK20 和 Ki67 在 CRC 组织中的表达明显高于正常结直肠组织。免疫染色评分显示,CD34 和 Ki67 与 CRC 的 UICC 分期和组织学分级显著相关(P < 0.05),但 CK19 和 CK20 与 UICC 分期和组织学分级无相关性(P > 0.05)。同时,CD34、CK19、CK20 和 Ki67 与 CRC 的位置无相关性(P > 0.05)。CD34 和 Ki67 高表达的患者生存最低(P < 0.05)。结果表明,CD34 和 Ki67 的共表达可能是 CRC 的一个重要特征,有助于预测 CRC 的进展。