Li Zheng-Rong, Wang Zhao, Zhu Bao-He, He Yu-Long, Peng Jun-Sheng, Cai Shi-Rong, Ma Jin-Ping, Zhan Wen-Hua
Department of Gastrointestinopancreatic Surgery, The First Affiliated Hospital, Sun Yat-sen University, Gastric Cancer Center of Sun Yat-sen University, No. 58 Zhongshan 2nd road, Guang Zhou 510080, China.
Surg Today. 2007;37(8):646-51. doi: 10.1007/s00595-006-3437-9. Epub 2007 Jul 26.
In gastric carcinoma, high expression of PRL-3, a protein tyrosine phosphatase, is associated with lymph node metastasis. We studied the relationship between PRL-3 expression and peritoneal metastasis in gastric carcinoma.
Immunohistochemical analysis using the anti-PRL-3 antibody was done in 639 patients with gastric carcinoma including 89 with peritoneal metastases. We then compared the clinicopathologic characteristics of the PRL-3-positive and PRL-3-negative carcinomas.
PRL-3 was expressed in 70.4% of the primary gastric carcinomas overall; in 80.9% of the cancers with peritoneal metastasis and in 68.7% of those without peritoneal metastasis (P = 0.020). PRL-3 expression was higher in peritoneal metastasis than in the corresponding primary gastric cancers (P = 0.028). PRL-3 expression was correlated with tumor stage (coefficient = 0.343, P = 0.01) and cancer progression, including lymphatic invasion (coefficient = 0.325, P = 0.02), extent of lymph node metastasis (coefficient = 0.322, P = 0.01), and peritoneal metastasis (coefficient = 0.316, P = 0.03). Patients who were PRL-3-negative had a better survival rate than those who were PRL-3-positive at all stages (stage I: log-rank P = 0.046, Wilcoxon P = 0.048; stage II: log-rank P = 0.035, Wilcoxon P = 0.041; stage III: log-rank P = 0.027, Wilcoxon P = 0.033; stage IV: log-rank P = 0.032, Wilcoxon P = 0.030).
Peritoneal metastasis appears to be correlated with PRL-3 expression, tumor stage, lymphatic invasion, and extent of lymph node metastasis. PRL-3 expression was negatively correlated with prognosis in patients with gastric cancer.
在胃癌中,蛋白酪氨酸磷酸酶PRL-3的高表达与淋巴结转移相关。我们研究了PRL-3表达与胃癌腹膜转移之间的关系。
对639例胃癌患者(包括89例有腹膜转移的患者)进行了使用抗PRL-3抗体的免疫组织化学分析。然后我们比较了PRL-3阳性和PRL-3阴性癌的临床病理特征。
总体上,70.4%的原发性胃癌表达PRL-3;有腹膜转移的癌症中80.9%表达PRL-3,无腹膜转移的癌症中68.7%表达PRL-3(P = 0.020)。PRL-3在腹膜转移中的表达高于相应的原发性胃癌(P = 0.028)。PRL-3表达与肿瘤分期(系数 = 0.343,P = 0.01)以及癌症进展相关,包括淋巴管浸润(系数 = 0.325,P = 0.02)、淋巴结转移范围(系数 = 0.322,P = 0.01)和腹膜转移(系数 = 0.316,P = 0.03)。在所有阶段,PRL-3阴性的患者比PRL-3阳性的患者生存率更高(I期:对数秩检验P = 0.046,Wilcoxon检验P = 0.048;II期:对数秩检验P = 0.035,Wilcoxon检验P = 0.041;III期:对数秩检验P = 0.027,Wilcoxon检验P = 0.033;IV期:对数秩检验P = 0.032,Wilcoxon检验P = 0.030)。
腹膜转移似乎与PRL-3表达、肿瘤分期、淋巴管浸润和淋巴结转移范围相关。PRL-3表达与胃癌患者的预后呈负相关。