Ebert M P, Yu J, Miehlke S, Fei G, Lendeckel U, Ridwelski K, Stolte M, Bayerdörffer E, Malfertheiner P
Department of Gastroenterolgy, Otto-von-Guericke University Magdeburg, Germany.
Br J Cancer. 2000 Jun;82(11):1795-800. doi: 10.1054/bjoc.1999.1107.
Transforming growth factors beta (TGF-beta) constitute a family of polypeptide growth factors that control cell growth, cell differentiation and migration, as well as the formation of the extracellular matrix. Recent analyses revealed the overexpression of TGF-beta1 in human gastric cancers and demonstrated increased cell proliferation in the stomach of patients with gastric cancer and their first-degree relatives. Using human gastric tissues obtained from patients with gastric cancer (n = 19), biopsies from healthy first-degree relatives of gastric cancer patients (n = 18) and healthy individuals (n = 19), we analysed the expression of TGF-beta1 using the reverse transcriptase polymerase chain reaction (RT-PCR) and immunohistochemistry. Fifteen of 19 patients with gastric cancer expressed TGF-beta1 in the tumour. In 11 of these 15 cases TGF-beta1 mRNA was also detectable in the non-tumourous stomach. Interestingly, all but two individuals with a first-degree relative diagnosed with gastric cancer exhibited TGF-beta1 expression in either the antrum or corpus biopsy or both. In contrast, only one of 19 individuals without a family history of gastric cancer expressed TGF-beta1 in the stomach (P< 0.0001). TGF-beta1 expression is detectable in a large proportion of gastric cancers and in the stomach of healthy first-degree relatives of gastric cancer patients. Since individuals without gastric cancers in their family express TGF-beta1 only in one of 19 cases, the induction of TGF-beta1 expression in first-degree relatives of patients with gastric cancer points to the presence of specific molecular alterations in a subgroup of individuals with an increased risk of developing gastric cancer that may precede the development of gastric cancers.
转化生长因子β(TGF-β)构成一类多肽生长因子家族,可控制细胞生长、细胞分化与迁移以及细胞外基质的形成。最近的分析显示,TGF-β1在人类胃癌中过度表达,并证实胃癌患者及其一级亲属胃内的细胞增殖增加。我们使用从胃癌患者(n = 19)、胃癌患者健康一级亲属的活检组织(n = 18)以及健康个体(n = 19)获取的人胃组织,通过逆转录聚合酶链反应(RT-PCR)和免疫组织化学分析了TGF-β1的表达。19例胃癌患者中有15例肿瘤组织表达TGF-β1。在这15例中的11例中,非肿瘤性胃组织中也可检测到TGF-β1 mRNA。有趣的是,除两名被诊断患有胃癌的一级亲属外,其他所有个体的胃窦或胃体活检组织或两者中均表现出TGF-β1表达。相比之下,19例无胃癌家族史的个体中只有1例胃内表达TGF-β1(P<0.0001)。在大部分胃癌以及胃癌患者健康一级亲属的胃组织中均可检测到TGF-β1表达。由于无胃癌家族史的个体中仅19例中有1例表达TGF-β1,因此胃癌患者一级亲属中TGF-β1表达的诱导表明,在胃癌发生风险增加的个体亚组中存在特定分子改变,这些改变可能先于胃癌的发生。