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由v-src癌基因诱导的肿瘤细胞在间充质分化标志物的表达上具有异质性。

Tumor cells induced by the v-src oncogene are heterogeneous for expression of markers of mesenchyme differentiation.

作者信息

England J M, Panella M J, Kopen G C, Wisner T W, Halpern M S

机构信息

Department of Pathology, Medical College of Pennsylvania, Philadelphia 19129.

出版信息

Virchows Arch. 1994;424(1):83-8. doi: 10.1007/BF00197397.

Abstract

The observation that v-src-induced tumors contain tumor cells of differing morphology, notably fibroblastoid or polygonal, raised the question as to whether the tumor cells are also heterogeneous with respect to expression of markers of cellular differentiation. Of the markers tested here, consistent reactivity for tumor tissue was noted only for antibody probes reactive to muscle actin (HHF35, alpha sm-1) or to procollagen type I (SP1. D8); for any given tumor, whether induced by v-src DNA or by Rous sarcoma virus, each of these markers was found only in a subpopulation of tumor cells. The observation of marker heterogeneity in the one v-src DNA-induced tumor examined here that typed as monoclonal suggests that v-src-induced transformation is consonant with a degree of plasticity in the phenotypes of the clonal progeny of a single transformant.

摘要

v-src诱导的肿瘤包含形态各异的肿瘤细胞,特别是成纤维细胞样或多边形细胞,这一观察结果引发了一个问题,即肿瘤细胞在细胞分化标志物的表达方面是否也存在异质性。在这里测试的标志物中,仅对与肌肉肌动蛋白(HHF35,α sm-1)或I型前胶原(SP1.D8)反应的抗体探针观察到肿瘤组织的一致反应性;对于任何给定的肿瘤,无论是由v-src DNA还是劳氏肉瘤病毒诱导的,这些标志物中的每一种仅在肿瘤细胞的一个亚群中发现。在这里检测的一例分型为单克隆的v-src DNA诱导肿瘤中观察到标志物异质性,这表明v-src诱导的转化与单个转化体的克隆后代表型的一定程度可塑性是一致的。

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