GnRH-II receptor-like antigenicity in human placenta and in cancers of the human reproductive organs

被引:27
作者
Eicke, N
Günthert, AR
Viereck, V
Siebold, D
Béhé, M
Becker, T
Emons, G
Gründker, C
机构
[1] Univ Gottingen, Dept Gynecol & Obstet, D-37075 Gottingen, Germany
[2] Univ Marburg, Dept Nucl Med, Marburg, Germany
[3] German Primate Ctr, Dept Vet Med & Primate Husbandry, Gottingen, Germany
关键词
D O I
10.1530/eje.1.02005
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
We have recently demonstrated that the antiproliferative activity of GnRH-II on human endometrial and ovarian cancer cell lines is not mediated through the GnRH-I receptor. A functional receptor for human GnRH-II has not yet been identified. In this study, we have generated a polyclonal antiserum to the putative human GnRH-II receptor using a peptide (YSPTMLTEVPPC) corresponding to the third extracellular domain coupled to keyhole limpet haemocyanin via the Cys residue. A database search showed no identical peptide sequences in any other human gene. To avoid cross-reactions against two similar amino acid sequences the antiserum was pre-absorbed using these peptides. Immune histological sections of human placenta and human endometrial, ovarian and prostate cancers using rabbit anti-human GnRH-II receptor antiserum showed GnRH-II receptor-like staining. Western blot analysis of cell membrane preparations of human endometrial and ovarian cancer cell lines yielded a band at approximately 43 kDa whereas Western blot analysis of cell membrane preparations of ovaries obtained from the marmoset monkey (Callithrix jacchus) yielded a band at approximately 54 kDa. To identify the GnRH-II receptor-like antigen we used the photo-affinity labelling technique. Photochemical reaction of I-125-labelled (4-azidobenzoyl)-N-hydroxysuccinimide-[D-LyS(6)]-GnRH-II (10(-9) M) with cell membrane preparations of human endometrial and ovarian cancer cells yielded a band at approximately 43kDa. In competition experiments, the GnRH-I agonist Triptorelin (10(-7) M) showed a weak decrease of I-125-labelled (4-azidobenzoyl)-N-hydroxysuccinimide-[D-LyS6]-GnRH-II binding to its binding site. The GnRH-I antagonist Cetrorelix (10(-7) M) showed a clearly stronger decrease, whereas GnRH-II agonist [D-Lys(6)]-GnRH-II (10(-7) M) was the most potent competitor. Western blot analysis of the same gel using rabbit anti-human GnRH-II receptor antiserum identified this band as GnRH-II receptor-like antigen.
引用
收藏
页码:605 / 612
页数:8
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