Targeted Ablation of Prostate Carcinoma Cells Through LH Receptor Using Hecate-CGβ Conjugate: Functional Characteristic and Molecular Mechanism of Cell Death Pathway
- 1 June 2005
- journal article
- Published by Frontiers Media SA in Experimental Biology and Medicine
- Vol. 230 (6) , 421-428
- https://doi.org/10.1177/15353702-0323006-10
Abstract
A Hecate-CGbeta conjugate (lytic peptide and beta-chorionic gonadotropin) selectively destroyed cells possessing LH receptors. This study described functional characteristics of the conjugate and the molecular mechanism of the cell death pathway in prostate cancer cells. Based on in vitro studies, we conclude that the conjugate kills cells possessing luteinizing hormone receptors (LHR) faster than Hecate alone. Competitive studies have shown that blocking of LHR by preincubation with chorionic gonadotropin (100 ng/ml) reduced toxicity of the conjugate in low concentrations. Further studies have also shown that the conjugate in treated cells both did not induce internucleosomal DNA fragmentation and did not induce morphological changes in cells characterized as having apoptotic features. These results proved that cells died by necrosis rather than apoptosis after the conjugate treatment.Keywords
This publication has 22 references indexed in Scilit:
- Targeted Destruction of Normal and Cancer Cells Through Lutropin/Choriogonadotropin Receptors Using Hecate-βCG ConjugateExperimental and Clinical Endocrinology & Diabetes, 2003
- A Novel Lytic Peptide Composed of dl-Amino Acids Selectively Kills Cancer Cells in Culture and in MiceJournal of Biological Chemistry, 2003
- Antimicrobial peptides of multicellular organismsNature, 2002
- Gene therapy for prostate cancerSeminars in Cancer Biology, 1997
- Expression of Luteinizing Hormone/Human Chorionic Gonadotropin Receptor Gene in Benign Prostatic Hyperplasia and in Prostate Carcinoma in HumansBiology of Reproduction, 1997
- The mouse inhibin α-subunit promoter directs SV40 T-antigen to Leydig cells in transgenic miceMolecular and Cellular Endocrinology, 1996
- A receptor binding site identified in the region 81–95 of the β-subunit of human luteinizing hormone (LH) and chorionic gonadotropin (hCG)Molecular and Cellular Endocrinology, 1993
- Carcinoma of the ProstateNew England Journal of Medicine, 1991
- Analysis of Events Associated With Cell Cycle Arrest at G2 Phase and Cell Death Induced by CisplatinJNCI Journal of the National Cancer Institute, 1990
- Establishment of gonadotropin-responsive murine leydig tumor cell line.The Journal of cell biology, 1982