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体外暴露于糖皮质激素的肝癌细胞中DNA合成的抑制

Suppression of DNA synthesis in hepatoma cells exposed to glucocorticoid hormone in vitro.

作者信息

Loeb J N, Borek C, Yeung L L

出版信息

Proc Natl Acad Sci U S A. 1973 Dec;70(12):3852-6. doi: 10.1073/pnas.70.12.3852.

Abstract

Glucocorticoid hormone is shown to markedly suppress DNA synthesis in a line of rat hepatoma cells in vitro. In the presence of 300 nM hydrocortisone or 30 nM dexamethasone the incorporation of radioactive thymidine falls to 50% of control levels by 36 hr, and at higher concentrations of hormone inhibition can be noted as early as 12 hr and is nearly complete by 24 hr. This inhibition of radioactive thymidine incorporation reflects a true suppression of DNA synthesis, is accompanied by a corresponding inhibition of cell proliferation, and is readily reversible upon subsequent removal of hormone. In contrast to previously described effects of the glucocorticoid hormones on various cells of lymphoid origin, the inhibition of DNA synthesis in these hepatoma cells is not accompanied by appreciable cell lysis or by degradation of preformed DNA, and even when [(3)H]thymidine incorporation into DNA is inhibited by 90% or more, incorporation of [(14)C]uridine into RNA proceeds with little change. These findings all parallel previous observations on the effects of glucocorticoid hormone on the livers of intact animals and suggest that studies on the mechanism of the inhibition of DNA synthesis in the present more isolated system may lead to a better understanding of the means by which these compounds inhibit liver growth in vivo. Despite the ready suppressibility of DNA synthesis in these hepatoma cells and in two other cell lines of liver origin, none of these cell lines was found to be inducible for tyrosine aminotransferase. The apparent dissociation between two "steroid-sensitive" phenomena is of interest and warrants further investigation.

摘要

糖皮质激素在体外可显著抑制大鼠肝癌细胞系中的DNA合成。在存在300 nM氢化可的松或30 nM地塞米松的情况下,放射性胸苷的掺入在36小时内降至对照水平的50%,在更高浓度的激素作用下,早在12小时就可观察到抑制作用,到24小时几乎完全抑制。放射性胸苷掺入的这种抑制反映了DNA合成的真正抑制,伴随着细胞增殖的相应抑制,并且在随后去除激素后很容易逆转。与先前描述的糖皮质激素对各种淋巴起源细胞的作用相反,这些肝癌细胞中DNA合成的抑制并不伴有明显的细胞裂解或预先形成的DNA降解,即使当[³H]胸苷掺入DNA被抑制90%或更多时,[¹⁴C]尿苷掺入RNA的过程几乎没有变化。这些发现都与先前关于糖皮质激素对完整动物肝脏作用的观察结果相似,并表明在目前这个更孤立的系统中对DNA合成抑制机制的研究可能有助于更好地理解这些化合物在体内抑制肝脏生长的方式。尽管这些肝癌细胞和另外两个肝脏起源的细胞系中的DNA合成很容易受到抑制,但没有发现这些细胞系中的任何一个可诱导产生酪氨酸转氨酶。这两种“类固醇敏感”现象之间明显的分离很有意思,值得进一步研究。

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