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人乳腺癌细胞系中的促性腺激素释放激素(GnRH)结合位点及GnRH拮抗剂的抑制作用

Gonadotropin-releasing hormone (GnRH)-binding sites in human breast cancer cell lines and inhibitory effects of GnRH antagonists.

作者信息

Eidne K A, Flanagan C A, Harris N S, Millar R P

出版信息

J Clin Endocrinol Metab. 1987 Mar;64(3):425-32. doi: 10.1210/jcem-64-3-425.

Abstract

GnRH-binding sites have previously been described in human breast tumors, and a GnRH agonist has been shown to inhibit growth of the MCF-7 human breast cancer cell line. We have investigated the presence of GnRH-binding sites in ZR-75-1, MDA-MB-231, Sk Br 3, MDA-MB-157, and MCF-7 human breast cancer cell lines and the effect of GnRH analogs on the incorporation of [3H]thymidine and 14C-labeled amino acids into DNA and protein. Specific GnRH-binding sites were present in membrane preparations of all five human breast carcinoma cell lines. Studies in three cell lines indicated low affinity (Kd, 1.6-3.0 X 10(-6) M) GnRH binding similar to that reported in human placenta and corpus luteum. In contrast, human pituitary GnRH receptors were of high affinity (Kd, 4.8 X 10(-9) M). Breast carcinoma cell GnRH-binding sites also differed from the pituitary receptor in their inability to discriminate between GnRH and superactive analogs. Binding of a [125I]GnRH analog to ZR-75-1 breast cancer cells and pituitary membranes was affected similarly by various cations. GnRH antagonists rapidly inhibited [3H]thymidine incorporation into DNA (within 3 hr), and this effect was reversible. GnRH antagonists also inhibited cell growth, but only after 6 days. GnRH agonists did not alter either thymidine incorporation or growth. The present observations of low affinity GnRH-binding sites in breast cancer cell lines and inhibitory effects of GnRH antagonists point to the possibility of an autocrine regulatory role of GnRH-like peptides in mammary cells.

摘要

此前已在人类乳腺肿瘤中描述过促性腺激素释放激素(GnRH)结合位点,并且已证明一种GnRH激动剂可抑制MCF-7人乳腺癌细胞系的生长。我们研究了ZR-75-1、MDA-MB-231、Sk Br 3、MDA-MB-157和MCF-7人乳腺癌细胞系中GnRH结合位点的存在情况,以及GnRH类似物对[3H]胸腺嘧啶核苷和14C标记氨基酸掺入DNA和蛋白质的影响。所有五种人乳腺癌细胞系的膜制剂中均存在特异性GnRH结合位点。对三种细胞系的研究表明,其GnRH结合亲和力较低(解离常数Kd为1.6 - 3.0×10(-6) M),类似于在人胎盘和黄体中报道的情况。相比之下,人垂体GnRH受体具有高亲和力(Kd为4.8×10(-9) M)。乳腺癌细胞的GnRH结合位点在区分GnRH和超活性类似物方面也与垂体受体不同。[125I]GnRH类似物与ZR-75-1乳腺癌细胞和垂体膜的结合受到各种阳离子的类似影响。GnRH拮抗剂可迅速抑制[3H]胸腺嘧啶核苷掺入DNA(3小时内),且这种作用是可逆的。GnRH拮抗剂也抑制细胞生长,但仅在6天后。GnRH激动剂既不改变胸腺嘧啶核苷掺入情况,也不影响细胞生长。目前在乳腺癌细胞系中观察到的低亲和力GnRH结合位点以及GnRH拮抗剂的抑制作用表明,GnRH样肽在乳腺细胞中可能具有自分泌调节作用。

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