Yanagihara K, Kamada N, Tsumuraya M, Amano F
Department of Pathology, Hiroshima University, Japan.
Int J Cancer. 1993 May 8;54(2):200-7. doi: 10.1002/ijc.2910540207.
We have established a human gastric scirrhous carcinoma cell line (designated as HSC-43) in a serum-free chemically defined medium (CDM) without any polypeptide growth factor, from a primary tumor of a 56-year-old male patient. HSC-43 cells grew in vitro in adherence with a population doubling time of 55 hr, and had the cytological properties of mucinous epithelial tumor cells. Cytogenetic analysis of the cells revealed pseudotetraploidy, with structural abnormalities of deletion at chromosome Iq25 and with 3 marker chromosomes. Some cells had retained features of signet-ring cells and caused fibroblastic proliferation when transplanted into athymic nude mice. The possible involvement of transforming growth factor-alpha (TGF-alpha), and its receptor, the epidermal-growth-factor receptor (EGFR), on the growth of HSC-43 cells was studied. Synthesis and secretion of TGF-alpha by HSC-43 cells were confirmed by biological assay and enzyme-linked immunosorbent assay. Radioreceptor analysis showed the presence of receptors for EGF in HSC-43 cells. Proliferation of HSC-43 cells was inhibited by antibodies against TGF-alpha and/or the EGFR. However, neither TGF-alpha nor epidermal growth factor (EGF) was effective in stimulating the cell growth of HSC-43 cells, irrespective of the cell density when supplemented exogenously. Our data suggest that TGF-alpha and EGFR play a role in the autocrine growth of HSC-43 cells. This may be another example of growth regulation of gastric carcinoma.
我们从一名56岁男性患者的原发性肿瘤中,在无任何多肽生长因子的无血清化学限定培养基(CDM)中建立了一种人胃硬癌细胞系(命名为HSC-43)。HSC-43细胞在体外贴壁生长,群体倍增时间为55小时,具有黏液上皮肿瘤细胞的细胞学特性。对这些细胞的细胞遗传学分析显示为假四倍体,在染色体1q25处有缺失的结构异常以及3条标记染色体。一些细胞保留了印戒细胞的特征,当移植到无胸腺裸鼠体内时会引起成纤维细胞增殖。研究了转化生长因子-α(TGF-α)及其受体表皮生长因子受体(EGFR)对HSC-43细胞生长的可能影响。通过生物学测定和酶联免疫吸附测定证实了HSC-43细胞合成和分泌TGF-α。放射受体分析表明HSC-43细胞中存在表皮生长因子(EGF)受体。抗TGF-α和/或EGFR的抗体可抑制HSC-43细胞的增殖。然而,无论外源补充时的细胞密度如何,TGF-α和表皮生长因子(EGF)均不能有效刺激HSC-43细胞的生长。我们的数据表明,TGF-α和EGFR在HSC-43细胞的自分泌生长中起作用。这可能是胃癌生长调节的另一个例子。