Leung Wai K, Yu Jun, Chan Francis K L, To Ka F, Chan Michael W Y, Ebert M P A, Ng Enders K W, Chung S C Sydney, Malfertheiner Peter, Sung Joseph J Y
Department of Medicine and Therapeutics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong.
J Pathol. 2002 Aug;197(5):582-8. doi: 10.1002/path.1147.
Trefoil factor family (TFF) domain peptides consist of three members that play a role in intestinal mucosal defence and repair, and in tumourigenesis. The role of the three TFF members in the gastric carcinogenesis cascade remains poorly defined. This study examined seven gastric cell lines, 50 gastric cancers and their adjacent non-cancer tissues, and tissues from 40 non-cancer patients, in order to elucidate the chronology of TFF expression in various stages of gastric carcinogenesis. TFF expression was determined by RT-PCR, immunohistochemistry, and western blot. Aberrant expression of TFF1, TFF2, and TFF3 was frequently detected in gastric cell lines. Specifically, TFF1 was detected in all non-cancer patients, but was detected in only 50% of gastric cancer and 66% of adjacent normal tissues. TFF2 expression was demonstrated in 87.5% of non-cancer patients, 34% of gastric carcinomas, and 58% of adjacent non-cancer tissues. There was a significant correlation between TFF1 and TFF2 expression in gastric cancer and adjacent non-cancer tissues (p<0.001). By contrast, TFF3 was detected in 25% of non-cancer patients and showed a predilection for areas with intestinal metaplasia (p=0.005). Sixty-two per cent of gastric cancers and 24% of neighbouring non-cancer tissues showed TFF3 expression. Immunoreactivity against TFF3 was demonstrated in goblet cells of intestinal metaplasia and within the cytoplasm and nuclei of tumour cells. Progressive loss of TFF1 and TFF2, together with the induction of TFF3, is likely to be involved in the early stage of the multi-step gastric carcinogenesis pathway.
三叶因子家族(TFF)结构域肽由三个成员组成,它们在肠道黏膜防御和修复以及肿瘤发生过程中发挥作用。这三个TFF成员在胃癌发生级联反应中的作用仍不清楚。本研究检测了七种胃癌细胞系、50例胃癌及其癌旁非癌组织以及40例非癌患者的组织,以阐明TFF在胃癌发生各阶段表达的时间顺序。通过逆转录聚合酶链反应(RT-PCR)、免疫组织化学和蛋白质印迹法测定TFF表达。在胃癌细胞系中经常检测到TFF1、TFF2和TFF3的异常表达。具体而言,在所有非癌患者中均检测到TFF1,但仅在50%的胃癌和66%的癌旁正常组织中检测到。87.5%的非癌患者、34%的胃癌和58%的癌旁非癌组织中显示有TFF2表达。胃癌及其癌旁非癌组织中TFF1和TFF2的表达之间存在显著相关性(p<0.001)。相比之下,25%的非癌患者中检测到TFF3,且TFF3在肠化生区域有偏好性表达(p=0.005)。62%的胃癌和24%的邻近非癌组织中有TFF3表达。在肠化生的杯状细胞以及肿瘤细胞的细胞质和细胞核内显示有针对TFF3的免疫反应性。TFF1和TFF2的逐渐缺失以及TFF3的诱导可能参与了胃癌多步骤发生途径的早期阶段。