Department of Pathology and Key Laboratory for Xinjiang Endemic and Ethnic Diseases, Shihezi University School of Medicine, North 4th Road, Shihezi, 832002, Xinjiang, People's Republic of China.
Med Oncol. 2014 Jan;31(1):791. doi: 10.1007/s12032-013-0791-5. Epub 2013 Dec 5.
This study investigated the expression of the phospholipase C epsilon 1 (PLCE1) and nuclear factor-kappaB (NF-κB)-related proteins in Kazakh patients with esophageal squamous cell carcinoma (ESCC). Tissue microarrays of 90 ethnic Kazakh patients with ESCC and exhibiting clinical characteristics were analyzed for protein expression of PLCE1, IKKβ, IKBα, p50, and p65 by immunohistochemistry. Correlations between histoscores of PLCE1 and NF-κB-related proteins were determined using Spearman's rank correlation tests. Expression of PLCE1 and NF-κB-related proteins significantly increased in tumor tissues compared with normal esophageal tissues (P = 9.48 × 10(-7), 1.24 × 10(-5), 0.004, 0.003, and 2.83 × 10(-5), respectively). Upregulation of PLCE1 was significantly correlated with advanced tumor-node-metastasis stages (P = 0.018) and lymph node metastasis (P = 0.003). Overexpression of IKKβ and IKBα was associated with ESCC stages I/II (P = 3.36 × 10(-4) and 0.022, respectively). Increased expression of p50 was significantly higher in patients with lymph node metastasis than without lymph node metastasis (P = 0.048). Elevated expression of p65 protein was significantly correlated with poor and moderately differentiated ESCC and depth of tumor invasion (P = 0.026 and 0.010, respectively). Significant positive correlations were observed between the expression of PLCE1 and NF-κB-related proteins, especially IKKβ (r = 0.246 and P = 0.025) and p50 (r = 0.244 and P = 0.024). These results suggest, for the first time, that upregulation of PLCE1 is correlated with increased expression of NF-κB-related proteins in Kazakh patients with ESCC, suggesting that interaction between PLCE1 with the NF-κB signal pathway may be responsible for the carcinogenesis of ESCC, such as ESCC-related inflammation.
本研究调查了磷脂酶 C ɛ 1(PLCE1)和核因子-κB(NF-κB)相关蛋白在哈萨克族食管鳞状细胞癌(ESCC)患者中的表达。通过免疫组织化学分析 90 例哈萨克族 ESCC 患者的组织微阵列,分析 PLCE1、IKKβ、IKBα、p50 和 p65 的蛋白表达。使用 Spearman 等级相关检验确定 PLCE1 和 NF-κB 相关蛋白的组织评分之间的相关性。与正常食管组织相比,肿瘤组织中 PLCE1 和 NF-κB 相关蛋白的表达显著增加(P=9.48×10(-7)、1.24×10(-5)、0.004、0.003 和 2.83×10(-5),分别)。PLCE1 的上调与肿瘤-淋巴结-转移(TNM)分期较高(P=0.018)和淋巴结转移(P=0.003)显著相关。IKKβ和 IKBα 的过表达与 ESCC I/II 期相关(P=3.36×10(-4)和 0.022,分别)。有淋巴结转移的患者 p50 的表达明显高于无淋巴结转移的患者(P=0.048)。p65 蛋白的高表达与 ESCC 低分化和中分化以及肿瘤浸润深度显著相关(P=0.026 和 0.010,分别)。PLCE1 与 NF-κB 相关蛋白的表达之间存在显著的正相关,尤其是 IKKβ(r=0.246,P=0.025)和 p50(r=0.244,P=0.024)。这些结果首次表明,哈萨克族 ESCC 患者中 PLCE1 的上调与 NF-κB 相关蛋白的表达增加相关,提示 PLCE1 与 NF-κB 信号通路的相互作用可能与 ESCC 的发生有关,例如与 ESCC 相关的炎症。