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人黑色素瘤细胞在无蛋白培养基中的连续培养:建立与部分特性研究

Continuous culture of human melanoma cells in protein-free medium: establishment and partial characterization.

作者信息

Urade M, Hamada S, Sugi M, Watatani K, Miyazaki T

出版信息

J Natl Cancer Inst. 1984 Nov;73(5):1039-48.

PMID:6593482
Abstract

Human melanoma cells (MEC) continuously grown in protein-free RPMI-1640 medium were established. These cultured cells, designated "sf-MEC," grow well in suspension and have been successfully subcultured more than 100 passages for 30 months with complete loss of serum requirement for their growth. Although sf-MEC as well as MEC had a moderate number of mature melanosomes in the cytoplasm, the tumorigenicity in nude mice was lower in sf-MEC than in MEC. In the tumor tissue formed by sf-MEC but not by MEC, a few immature melanosomes and an increased C-type-like virus production were detected. Furthermore, conditioned medium of sf-MEC stimulated DNA synthesis in both normal and transformed cells, including MEC and sf-MEC. Addition of the conditioned medium of sf-MEC in its cell growth assay caused a twofold to eighteenfold increase in cell number as compared to that for the control.

摘要

建立了在无蛋白RPMI-1640培养基中持续生长的人黑色素瘤细胞(MEC)。这些培养的细胞被命名为“sf-MEC”,能在悬浮状态下良好生长,并且在30个月内已成功传代100多次,其生长完全不再需要血清。尽管sf-MEC和MEC在细胞质中都有中等数量的成熟黑素小体,但sf-MEC在裸鼠中的致瘤性低于MEC。在由sf-MEC而非MEC形成的肿瘤组织中,检测到一些未成熟的黑素小体和增加的C型样病毒产生。此外,sf-MEC的条件培养基刺激正常细胞和转化细胞(包括MEC和sf-MEC)中的DNA合成。在其细胞生长试验中添加sf-MEC的条件培养基,与对照组相比,细胞数量增加了两倍至十八倍。

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