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[人类胃癌中的癌基因]

[Oncogenes in human gastric carcinoma].

作者信息

Tahara E

机构信息

Dept. of Pathology, Hiroshima University School of Medicine.

出版信息

Gan To Kagaku Ryoho. 1989 Jun;16(6):2149-55.

PMID:2544146
Abstract

Alteration of oncogene and loss of chromosomal heterozygosity are infrequent in human gastric carcinoma compared with those in other gastrointestinal carcinomas. Amplification of c-erbB-2 gene is observed in well differentiated adenocarcinoma, while sam gene is found in poorly differentiated adenocarcinoma or scirrhous carcinoma. sam gene, which was isolated from a gastric cancer cell line KATO-III by a DNA renaturation method, encodes tyrosine-specific protein kinase domain. A good correlation evidently exists between the synchronous expression of TGF alpha and ras p21 and biological malignancy of gastric carcinoma. c-myc and c-fos proteins are found not only in tumor cells but also in stromal cells including macrophages and fibroblast around the tumors. The prognosis of patients with c-myc p 62-positive stromal cells is significantly better than that of patient with p 62-negative stromal cells. Coamplification of the hst-1 gene and int-2 is observed in 50% of primary tumors and all metastatic tumors of esophageal carcinoma. PCR (polymerase chain reaction) technique seems to be useful for the detection of oncogene point mutation in human gastric carcinoma.

摘要

与其他胃肠道癌相比,癌基因改变和染色体杂合性缺失在人类胃癌中并不常见。在高分化腺癌中观察到c-erbB-2基因扩增,而在低分化腺癌或硬癌中发现sam基因。通过DNA复性方法从胃癌细胞系KATO-III中分离出的sam基因编码酪氨酸特异性蛋白激酶结构域。TGFα和ras p21的同步表达与胃癌的生物学恶性程度之间显然存在良好的相关性。c-myc和c-fos蛋白不仅存在于肿瘤细胞中,也存在于包括肿瘤周围巨噬细胞和成纤维细胞在内的基质细胞中。c-myc p62阳性基质细胞患者的预后明显优于p62阴性基质细胞患者。在50%的食管癌原发性肿瘤和所有转移性肿瘤中观察到hst-1基因和int-2的共扩增。聚合酶链反应(PCR)技术似乎有助于检测人类胃癌中的癌基因点突变。

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