Effects of ligand activation of peroxisome proliferator-activated receptor γ in human prostate cancer

被引:386
作者
Mueller, E
Smith, M
Sarraf, P
Kroll, T
Aiyer, A
Kaufman, DS
Oh, W
Demetri, G
Figg, WD
Zhou, XP
Eng, C
Spiegelman, BM
Kantoff, PW
机构
[1] Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Div Hematol Oncol, Boston, MA 02114 USA
[4] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Pathol, Boston, MA 02115 USA
[5] Harvard Univ, Brigham & Womens Hosp, Dana Farber Canc Inst, Dept Adult Oncol, Boston, MA 02115 USA
[6] NCI, Med Branch, NIH, Bethesda, MD 20892 USA
[7] Ohio State Univ, Ctr Comprehens Canc, Human Canc Genet Program, Columbus, OH 43210 USA
关键词
D O I
10.1073/pnas.180329197
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Peroxisome proliferator-activated receptor gamma (PPAR gamma) is a nuclear hormone receptor that plays a key role in the differentiation of adipocytes. Activation of this receptor in liposarcomas and breast and colon cancer cells also induces cell growth inhibition and differentiation. In the present study, we show that PPAR gamma is expressed in human prostate adenocarcinomas and cell lines derived from these tumors. Activation of this receptor with specific ligands exerts an inhibitory effect on the growth of prostate cancer cell lines. Further, we show that prostate cancer and cell lines do not have intragenic mutations in the PPAR gamma gene, although 40% of the informative tumors have hemizygous deletions of this gene. Based on our preclinical data, we conducted a phase II clinical study in patients with advanced prostate cancer using troglitazone, a PPAR gamma ligand used for the treatment of type 2 diabetes. Forty-one men with histologically confirmed prostate cancer and no symptomatic metastatic disease were treated orally with troglitazone. An unexpectedly high incidence of prolonged stabilization of prostate-specific antigen was seen in patients treated with troglitazone. In addition, one patient had a dramatic decrease in serum prostate-specific antigen to nearly undetectable levels. These data suggest that PPAR gamma may serve as a biological modifier in human prostate cancer and its therapeutic potential in this disease should be further investigated.
引用
收藏
页码:10990 / 10995
页数:6
相关论文
共 26 条
[1]   Activation of PPARγ leads to inhibition of anchorage-independent growth of human colorectal cancer cells [J].
Brockman, JA ;
Gupta, RA ;
DuBois, RN .
GASTROENTEROLOGY, 1998, 115 (05) :1049-1055
[2]   PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR (PPAR)-GAMMA - ADIPOSE-PREDOMINANT EXPRESSION AND INDUCTION EARLY IN ADIPOCYTE DIFFERENTIATION [J].
CHAWLA, A ;
SCHWARZ, EJ ;
DIMACULANGAN, DD ;
LAZAR, MA .
ENDOCRINOLOGY, 1994, 135 (02) :798-800
[3]   Induction of solid tumor differentiation by the peroxisome proliferator-activated receptor-γ ligand troglitazone in patients with liposarcoma [J].
Demetri, GD ;
Fletcher, CDM ;
Mueller, E ;
Sarraf, P ;
Naujoks, R ;
Campbell, N ;
Spiegelman, BM ;
Singer, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (07) :3951-3956
[4]   Troglitazone improves defects in insulin action, insulin secretion, ovarian steroidogenesis, and fibrinolysis in women with polycystic ovary syndrome [J].
Ehrmann, DA ;
Schneider, DJ ;
Sobel, BE ;
Cavaghan, MK ;
Imperial, J ;
Rosenfield, RL ;
Polonsky, KS .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (07) :2108-2116
[5]   Ligands for peroxisome proliferator-activated receptorγ and retinoic acid receptor inhibit growth and induce apoptosis of human breast cancer cells in vitro and in BNX mice [J].
Elstner, E ;
Müller, C ;
Koshizuka, K ;
Williamson, EA ;
Park, D ;
Asou, H ;
Shintaku, P ;
Said, JW ;
Heber, D ;
Koeffler, HP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (15) :8806-8811
[6]   15-DEOXY-DELTA(12,14)-PROSTAGLANDIN J(2) IS A LIGAND FOR THE ADIPOCYTE DETERMINATION FACTOR PPAR-GAMMA [J].
FORMAN, BM ;
TONTONOZ, P ;
CHEN, J ;
BRUN, RP ;
SPIEGELMAN, BM ;
EVANS, RM .
CELL, 1995, 83 (05) :803-812
[7]  
Gioeli D, 1999, CANCER RES, V59, P279
[8]   Inhibition of adipogenesis through MAP kinase-mediated phosphorylation of PPAR gamma [J].
Hu, ED ;
Kim, JB ;
Sarraf, P ;
Spiegelman, BM .
SCIENCE, 1996, 274 (5295) :2100-2103
[9]   Fatty acids and eicosanoids regulate gene expression through direct interactions with peroxisome proliferator-activated receptors alpha and gamma [J].
Kliewer, SA ;
Sundseth, SS ;
Jones, SA ;
Brown, PJ ;
Wisely, GB ;
Koble, CS ;
Devchand, P ;
Wahli, W ;
Willson, TM ;
Lenhard, JM ;
Lehmann, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (09) :4318-4323
[10]   A PROSTAGLANDIN J(2) METABOLITE BINDS PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-GAMMA AND PROMOTES ADIPOCYTE DIFFERENTIATION [J].
KLIEWER, SA ;
LENHARD, JM ;
WILLSON, TM ;
PATEL, I ;
MORRIS, DC ;
LEHMANN, JM .
CELL, 1995, 83 (05) :813-819