Zhang J, Zhang R, Lu W W, Zhu J S, Xia L Q, Lu Y M, Chen N W
Department of Gastroenterology, Shanghai Sixth Peoples Hospital Affiliated to Shanghai Jiao Tong University, Shanghai, China.
Int J Immunopathol Pharmacol. 2014 Oct-Dec;27(4):543-51. doi: 10.1177/039463201402700410.
High mobility group box 1 (HMGB1) has been proved to be implicated in a variety of cell physiological and pathological behaviors including immune response, inflammation and cancer. Accumulating evidence suggests that HMGB1 plays a critical role in the development and progression of multiple malignancies. However, the clinical significance and prognosis of HMGB1 expression in some cancers remain controversial. The present study aimed to investigate whether overexpression of HMGB1 is an independent prognostic factor in patients with gastric cancer. The correlation of HMGB1 expression with clinicopathologic characteristics and prognosis was assessed by immunohistochemical assay through tissue microarray procedure in 50 primary gastric cancer cases. Our results indicated that the positive expression of HMGB1 was significantly increased in the nucleus of gastric cancer tissues compared with the adjacent non-cancerous tissues (ANCT) (64.0% vs 44.0%, P=0.025), but was not linked to the clinicopathologic features, including the TNM stage (P=0.533) and metastatic lymph node (P=0.771), in patients with gastric cancer. Kapalan-Meier and log-rank analysis demonstrated that overexpression of HMGB1 did not exert significant impact on the overall survival of patients with gastric cancer (P=0.805). Furthermore, Cox regression analysis showed that high HMGB1 protein expression did not represent an independent risk factor for patients with gastric cancer (P=0.677). Taken together, our findings suggest that high expression of HMGB1 is not correlated with the clinicopathologic characteristics of gastric cancer, and cannot serve as an independent prognostic biomarker for patients with gastric cancer.
高迁移率族蛋白B1(HMGB1)已被证明与多种细胞生理和病理行为有关,包括免疫反应、炎症和癌症。越来越多的证据表明,HMGB1在多种恶性肿瘤的发生和发展中起关键作用。然而,HMGB1在某些癌症中的临床意义和预后仍存在争议。本研究旨在探讨HMGB1过表达是否是胃癌患者的独立预后因素。通过组织芯片技术,采用免疫组化方法评估了50例原发性胃癌病例中HMGB1表达与临床病理特征及预后的相关性。我们的结果表明,与癌旁非癌组织(ANCT)相比,胃癌组织细胞核中HMGB1的阳性表达显著增加(64.0%对44.0%,P=0.025),但与胃癌患者的临床病理特征无关,包括TNM分期(P=0.533)和转移淋巴结(P=0.771)。Kaplan-Meier和对数秩分析表明,HMGB1过表达对胃癌患者的总生存期没有显著影响(P=0.805)。此外,Cox回归分析显示,高HMGB1蛋白表达不是胃癌患者的独立危险因素(P=0.677)。综上所述,我们的研究结果表明,HMGB1的高表达与胃癌的临床病理特征无关,不能作为胃癌患者的独立预后生物标志物。