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培养的人骨肉瘤和软骨肉瘤细胞对视黄酸的敏感性。

Sensitivity of cultured human osteosarcoma and chondrosarcoma cells to retinoic acid.

作者信息

Thein R, Lotan R

出版信息

Cancer Res. 1982 Nov;42(11):4771-5.

PMID:6957261
Abstract

The ability of retinoic acid (RA) to inhibit the growth of three cell lines (Te85, Hs781, and Hs791) derived from human osteosarcomas and two cell lines (Hs705 and Hs819) derived from human chondrosarcomas was studied in culture. The exposure to 10(-5) M RA resulted, within 4 days, in changes in both cell morphology and cell growth. RA-treated cells appeared flat and spread on the substratum more than untreated cells, their exponential growth rates decreased, and their saturation densities were markedly reduced. All these effects could be reversed by removal of RA from the growth medium. The various cell lines exhibited differential susceptibility to the growth-inhibitory effect of RA. The most sensitive was the Hs705 chondrosarcoma. The proliferation of these cells was inhibited 50% by 10(-9) M RA and was completely blocked by 10(-5) m RA. In contrast, the concentrations of RA required for 50% inhibition of Hs791, Te85, Hs819, and Hs781 were 10(-7), 2 X 10(-7), 2.5 X 10(-7), and 2 X 10(-6) M, respectively. Only the Te85 and the Hs781 osteosarcoma cells and cells derived from a chondrosarcoma biopsy were able to form colonies in a semisolid medium, and this growth was dramatically inhibited by RA. These results demonstrate that RA can suppress in these mesenchymal tumor cells the expression of morphological and growth properties frequently associated with transformed cells.

摘要

在培养过程中研究了视黄酸(RA)抑制源自人骨肉瘤的三种细胞系(Te85、Hs781和Hs791)以及源自人软骨肉瘤的两种细胞系(Hs705和Hs819)生长的能力。暴露于10^(-5) M的RA后,在4天内细胞形态和细胞生长均发生变化。经RA处理的细胞比未处理的细胞显得更扁平且在基质上铺展得更开,其指数生长速率降低,饱和密度显著降低。从生长培养基中去除RA后,所有这些效应均可逆转。各种细胞系对RA的生长抑制作用表现出不同的敏感性。最敏感的是Hs705软骨肉瘤细胞。这些细胞的增殖在10^(-9) M RA作用下被抑制50%,在10^(-5) M RA作用下完全被阻断。相比之下,对Hs791、Te85、Hs819和Hs781细胞50%抑制所需的RA浓度分别为10^(-7)、2×10^(-7)、2.5×10^(-7)和2×10^(-6) M。只有Te85和Hs781骨肉瘤细胞以及源自软骨肉瘤活检的细胞能够在半固体培养基中形成集落,而这种生长受到RA的显著抑制。这些结果表明,RA可以抑制这些间充质肿瘤细胞中通常与转化细胞相关的形态和生长特性的表达。

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