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胰腺癌细胞核中促黄体激素释放激素(LH-RH)受体的浓度。(D-色氨酸6)促黄体激素释放激素对荷瘤叙利亚金黄地鼠的影响。

The concentration of LH-RH receptors in the nuclei of pancreatic cancer cells. Effect of (D-Trp6)LH-RH on tumor-bearing Syrian golden hamsters.

作者信息

Szende B, Csikós A, Szepeshazi K, Neill J D, Mulchahey J J, Halmos G, Lapis K, Schally A V

机构信息

Institute of Pathology and Experimental Cancer Research, Semmelweis University of Medicine, Budapest, Hungary.

出版信息

Receptor. 1994 Winter;4(4):201-7.

PMID:7894336
Abstract

LH-RH analogs cause some inhibition of growth of pancreatic cancers. Syrian golden hamsters bearing chemically induced pancreatic cancers were treated with [D-Trp6]LH-RH for 3 d before sacrifice. LH-RH receptors were localized by electron-microscopic immunohistochemistry in the tumor cells of both treated and untreated hamsters. [D-Trp6]LH-RH treatment resulted in a marked increase in the concentration of LH-RH receptors in the nuclei. The dissociation constants (Kd) and the maximal binding capacity of the LH-RH receptors (Bmax), measured by radioreceptor assay, were higher in the nuclei of the pancreatic tumor cells of hamsters treated with [D-Trp6]LH-RH than in the untreated controls. Pancreatic cells of tumor-free hamsters did not show immunostaining for LH-RH receptors. A possible correlation between the increase in the concentration of the LH-RH receptors in the nuclei and the tumor growth-inhibiting activity of [D-Trp6]LH-RH is suggested.

摘要

促黄体生成素释放激素(LH-RH)类似物对胰腺癌的生长有一定抑制作用。对携带化学诱导胰腺癌的叙利亚金黄地鼠在处死前用[D-色氨酸6]LH-RH处理3天。通过电子显微镜免疫组织化学法在经处理和未经处理的地鼠肿瘤细胞中定位LH-RH受体。[D-色氨酸6]LH-RH处理导致细胞核中LH-RH受体浓度显著增加。通过放射受体分析法测得,经[D-色氨酸6]LH-RH处理的地鼠胰腺肿瘤细胞核中LH-RH受体的解离常数(Kd)和最大结合容量(Bmax)高于未处理的对照组。无肿瘤地鼠的胰腺细胞未显示出LH-RH受体的免疫染色。提示细胞核中LH-RH受体浓度的增加与[D-色氨酸6]LH-RH的肿瘤生长抑制活性之间可能存在相关性。

相似文献

1
The concentration of LH-RH receptors in the nuclei of pancreatic cancer cells. Effect of (D-Trp6)LH-RH on tumor-bearing Syrian golden hamsters.胰腺癌细胞核中促黄体激素释放激素(LH-RH)受体的浓度。(D-色氨酸6)促黄体激素释放激素对荷瘤叙利亚金黄地鼠的影响。
Receptor. 1994 Winter;4(4):201-7.
2
Presence of membrane binding sites for [D-TRP6]-luteinizing hormone-releasing hormone in experimental pancreatic cancer.实验性胰腺癌中[D-色氨酸6]-促黄体生成素释放激素膜结合位点的存在
Cancer Lett. 1989 May;45(2):87-91. doi: 10.1016/0304-3835(89)90141-9.
3
Regression of nitrosamine-induced pancreatic cancers in hamsters treated with luteinizing hormone-releasing hormone antagonists or agonists.用促黄体生成素释放激素拮抗剂或激动剂治疗的仓鼠中,亚硝胺诱导的胰腺癌的消退。
Cancer Res. 1990 Jun 15;50(12):3716-21.
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Membrane receptors for peptides in experimental and human pancreatic cancers.实验性和人类胰腺癌中肽的膜受体
Pancreas. 1989;4(5):521-8. doi: 10.1097/00006676-198910000-00001.
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Detection and partial characterization of receptors for [D-Trp6]-luteinizing hormone-releasing hormone and epidermal growth factor in human endometrial carcinoma.人子宫内膜癌中[D-色氨酸6]-促黄体生成素释放激素及表皮生长因子受体的检测与部分特性分析
Cancer Res. 1990 Mar 15;50(6):1841-6.
6
Treatment of N-nitrosobis(2-oxopropyl)amine-induced pancreatic cancer in Syrian golden hamsters with D-Trp-6-LH-RH and somatostatin analogue RC-160 microcapsules.用D-色氨酸-6-促黄体生成素释放激素和生长抑素类似物RC-160微胶囊治疗叙利亚金黄地鼠N-亚硝基双(2-氧代丙基)胺诱导的胰腺癌
Cancer Res. 1989 Apr 1;49(7):1810-5.
7
Inhibitory effect of bombesin/gastrin-releasing peptide antagonist RC-3095 and high dose of somatostatin analogue RC-160 on nitrosamine-induced pancreatic cancers in hamsters.蛙皮素/胃泌素释放肽拮抗剂RC - 3095和高剂量生长抑素类似物RC - 160对亚硝胺诱导的仓鼠胰腺癌的抑制作用。
Cancer Res. 1991 Nov 1;51(21):5980-6.
8
Treatment of nitrosamine-induced pancreatic tumors in hamsters with analogs of somatostatin and luteinizing hormone-releasing hormone.用生长抑素类似物和促黄体生成素释放激素类似物治疗仓鼠亚硝胺诱导的胰腺肿瘤。
Proc Natl Acad Sci U S A. 1987 Feb;84(4):1112-6. doi: 10.1073/pnas.84.4.1112.
9
Combination treatment of nitrosamine-induced pancreatic cancers in hamsters with analogs of LH-RH and a bombesin/GRP antagonist.用促黄体生成素释放激素类似物和一种蛙皮素/胃泌素释放肽拮抗剂联合治疗仓鼠亚硝胺诱导的胰腺癌。
Int J Pancreatol. 1994 Oct-Dec;16(2-3):141-9. doi: 10.1007/BF02944324.
10
Receptors for D-Trp6-luteinizing hormone-releasing hormone, somatostatin, and insulin-like growth factor I in MXT mouse mammary carcinoma.MXT小鼠乳腺癌中D-色氨酸6-促黄体生成素释放激素、生长抑素和胰岛素样生长因子I的受体
Proc Soc Exp Biol Med. 1989 Dec;192(3):209-18. doi: 10.3181/00379727-192-42987.

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The human gonadotropin releasing hormone type I receptor is a functional intracellular GPCR expressed on the nuclear membrane.人类促性腺激素释放激素 I 型受体是一种功能性的细胞内 G 蛋白偶联受体,表达于核膜上。
PLoS One. 2010 Jul 8;5(7):e11489. doi: 10.1371/journal.pone.0011489.
2
Identification of a gonadotropin-releasing hormone receptor orthologue in Caenorhabditis elegans.秀丽隐杆线虫中促性腺激素释放激素受体同源物的鉴定。
BMC Evol Biol. 2006 Nov 29;6:103. doi: 10.1186/1471-2148-6-103.
3
Changes in subcellular distribution of pituitary receptors for luteinizing hormone-releasing hormone (LH-RH) after treatment with the LH-RH antagonist cetrorelix.
用促黄体生成激素释放激素(LH-RH)拮抗剂西曲瑞克治疗后垂体促黄体生成激素释放激素(LH-RH)受体亚细胞分布的变化。
Proc Natl Acad Sci U S A. 2002 Jan 22;99(2):961-5. doi: 10.1073/pnas.012598399.
4
A specifically radiolabeled somatostatin analog with strong antitumor activity induces apoptosis and accumulates in the cytosol and the nucleus of HT29 human colon carcinoma cells.一种具有强抗肿瘤活性的特异性放射性标记生长抑素类似物可诱导HT29人结肠癌细胞凋亡,并在其细胞质和细胞核中蓄积。
Endocrine. 1999 Feb;10(1):25-34. doi: 10.1385/ENDO:10:1:25.