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SV40诱导的转化和致瘤性在小鼠细胞杂交体中的非协同表达。

Noncoordinate expression of SV40-induced transformation and tumorigenicity in mouse cell hybrids.

作者信息

Howell N, Sager R

出版信息

Somatic Cell Genet. 1979 Jan;5(1):129-43. doi: 10.1007/BF01538791.

Abstract

Somatic mouse cells hybrids formed by fusion of nontumorigenic 3T3 closely related SV40-transformed SVT2 cells were analyzed in a study designed to probe the genetic basis of the multiple phenotypic changes induced by SV40 transformation. These hybrids showed noncoordinate expression of the transformation phenotype. Although they cloned at high efficiency in medium with low serum and expressed the SV40 T-antigen of the SVT2 parent, hybrid cells grew poorly without anchorage and exhibited a cell and colony morphology intermediate between that of the parents. Tumorigenicity was assayed quantitatively by subcutaneous coinjection into athymic nude mice of serial dilutions of 10(2) to 10(5) hybrid cells with 10(7) lethally irradiated 3T3 cells. The results showed that 100--1000 times more hybrid cells had to be injected for tumor formation than were required with SVT2. These and other observations show that most 3T3/SVT2 hybrid cells are not tumorigenic but that each population contains a rare subset of tumorigenic cells.

摘要

在一项旨在探究由SV40转化诱导的多种表型变化的遗传基础的研究中,对通过非致瘤性3T3细胞与密切相关的SV40转化的SVT2细胞融合形成的体细胞小鼠细胞杂种进行了分析。这些杂种表现出转化表型的不协调表达。尽管它们在低血清培养基中能高效克隆并表达SVT2亲本的SV40 T抗原,但杂种细胞在无锚定条件下生长不佳,并且表现出介于亲本之间的细胞和集落形态。通过将10²至10⁵个杂种细胞的系列稀释液与10⁷个经致死剂量照射的3T3细胞皮下共注射到无胸腺裸鼠中来定量测定致瘤性。结果表明,与SVT2相比,形成肿瘤所需注射的杂种细胞数量要多100至1000倍。这些以及其他观察结果表明,大多数3T3/SVT2杂种细胞不具有致瘤性,但每个群体中都含有一小部分罕见的致瘤细胞亚群。

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