Wu Zhiming, Zhang Lin, Li Nan, Sha Lina, Zhang Kunpeng
Department of Gastroenterology and Hepatology, The 309 Hospital of People's Liberation Army, Beijing 100091, P.R. China ; Hebei North University, Zhangjiakou, Hebei 073000, P.R. China.
Department of Gastroenterology and Hepatology, The 309 Hospital of People's Liberation Army, Beijing 100091, P.R. China.
Oncol Lett. 2015 Mar;9(3):1154-1158. doi: 10.3892/ol.2014.2832. Epub 2014 Dec 29.
Thioredoxin domain-containing 5 (TXNDC5) is overexpressed in a number of human carcinomas. However, the involvement of TXNDC5 in gastric adenocarcinoma remains unclear. In the present study, the immunohistochemical expression and clinicopathological significance of TXNDC5 in gastric adenocarcinoma was investigated. The immunohistochemical expression of TXNDC5 was detected in 54 gastric adenocarcinoma specimens, and the correlation between TXNDC5 and the clinicopathological features was investigated. Of the 54 gastric adenocarcinoma specimens, 30 samples (55.6%) exhibited high TXNDC5 expression. In the adenocarcinoma specimens exhibiting high TXNDC5 expression, the proportion of poorly-differentiated adenocarcinomas was significantly higher than that in specimens exhibiting low TXNDC5 expression (P<0.05). Lymph node metastasis and the depth of tumor invasion in the specimens exhibiting high TXNDC5 expression were significantly higher than that in specimens exhibiting low TXNDC5 expression (P<0.05). The results of a survival analysis revealed that the prognosis of patients exhibiting high TXNDC5 expression was significantly poorer than that of patients exhibiting low TXNDC5 expression (P<0.05). Therefore, the expression of TXNDC5 may correlate with the differentiation, invasion and metastasis of gastric adenocarcinoma. Thus, TXNDC5 may be a tumor-enhancing gene that is involved in gastric cancer.
含硫氧还蛋白结构域5(TXNDC5)在多种人类癌症中过表达。然而,TXNDC5在胃腺癌中的作用仍不清楚。在本研究中,调查了TXNDC5在胃腺癌中的免疫组化表达及临床病理意义。检测了54例胃腺癌标本中TXNDC5的免疫组化表达,并研究了TXNDC5与临床病理特征之间的相关性。在54例胃腺癌标本中,30例(55.6%)表现出TXNDC5高表达。在TXNDC5高表达的腺癌标本中,低分化腺癌的比例显著高于TXNDC5低表达的标本(P<0.05)。TXNDC5高表达标本中的淋巴结转移和肿瘤浸润深度显著高于TXNDC5低表达的标本(P<0.05)。生存分析结果显示,TXNDC5高表达患者的预后明显差于TXNDC5低表达患者(P<0.05)。因此,TXNDC5的表达可能与胃腺癌的分化、侵袭和转移相关。因此,TXNDC5可能是一种参与胃癌的肿瘤增强基因。