Anticancer Activity of a New Gonadotropin Releasing Hormone Analogue

被引:7
作者
Saleh-Abady, Mohammad Mirzaei [1 ]
Naderi-Manesh, Hossein [1 ]
Alizadeh, Abdolali [2 ]
Shamsipour, Fereshteh [3 ]
Balalaie, Saeed [4 ]
Arabanian, Armin [4 ]
机构
[1] Tarbiat Modares Univ, Dept Biophys, Fac Basic Sci, Tehran, Iran
[2] Tarbiat Modares Univ, Dept Chem, Fac Basic Sci, Tehran, Iran
[3] Avicenna Res Inst, Monoclonal Antibody Res Ctr, Tehran, Iran
[4] KN Toosi Univ Technol, Peptide Chem Res Grp, Tehran, Iran
关键词
LHRH analogue; triptorelin; peptidomimetics; anticancer activity; ovarian cancer; breast cancer; APOPTOTIC CELL-DEATH; OVARIAN-CANCER CELLS; HUMAN ENDOMETRIAL; GNRH ANTAGONISTS; IN-VITRO; RECEPTOR; PROLIFERATION; EXPRESSION; (GNRH)-I; CULTURES;
D O I
10.1002/bip.21335
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Gonadotropin releasing hormone (GnRH) has a pivotal role in the biology of reproduction processes. In extrapituitary compartments GnRH and its receptor act as a part of the autocrin regulatory system of cell proliferation, resulting in its anticancer activity. Here the anticancer activity of a new analogue of GnRH has been investigated. Results indicate that proliferation of human breast and ovarian cancer cell lines is dose-dependently inhibited. The inhibitory efficiency of this new analogue is proved to be higher than the original triptorelin. In addition to its antimitogenic activity, evidence was found for the involvement of the apoptotic mechanism in the action of the new analogue. Furthermore the presence of chemical groups in the peptide sequence is thought to increase the protease stability of the new analogue in comparison with triptorelin. Consequently our new analogue can be considered as a good pharmaceutical candidate. (C) 2009 Wiley Periodicals, Inc. Biopolymers (Pept Sci) 94: 292-297, 2010.
引用
收藏
页码:292 / 297
页数:6
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