Leukotoxin diols from ground corncob bedding disrupt estrous cyclicity in rats and stimulate MCF-7 breast cancer cell proliferation

被引:40
作者
Markaverich, BM
Crowley, JR
Alejandro, MA
Shoulars, K
Casajuna, N
Mani, S
Reyna, A
Sharp, J
机构
[1] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Ctr Comparat Med, Houston, TX 77030 USA
[3] Washington Univ, Sch Med, Dept Mass Spectrometry Facil, St Louis, MO USA
关键词
breast cancer; corncob bedding; endocrine disruptor; estrous cycles; leukotoxin diols;
D O I
10.1289/ehp.8231
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Previous studies in our laboratory demonstrated that high-performance liquid chromatography (HPLC) analysis of ground corncob bedding extracts characterized two components (peak I and peak II) that disrupted endocrine function in male and female rats and stimulated breast and prostate cancer cell proliferation in vitro and in vivo. The active substances in peak 1 were identified as an isomeric mixture of 9,12-oxy- 10, 13-dihydroxyoctadecanoic acid and 10, 13-oxy-9,12-dihydroxyoctadecanoic acid, collectively designated tetrahydrofurandiols (THF-diols). Studies presented here describe the purification and identification of the HPLC peak II component as 9,10-dihydroxy-12-octadecenoic acid (leukotoxin diol; LTX-diol), a well-known leukotoxin. A synthetic mixture of LTX-diol and 12,13-dihydroxy-9-octadecenoic acid (iso-leukotoxin diol; i-LTX-diol) isomers was separated by HPLC, and each isomer stimulated (p < 0.001) MCF-7 cell proliferation in an equivalent fashion. The LTX-diol isomers failed to compete for [H-3]estradiol binding to the estrogen receptor or nuclear type II sites, even though oral administration of very low doses of these compounds (>> 0.8 mg/kg body weight/day) disrupted estrous cyclicity in female rats. The LTX-diols did not disrupt male sexual behavior, suggesting that sex differences exist in response to these endocrine-disruptive agents.
引用
收藏
页码:1698 / 1704
页数:7
相关论文
共 42 条
[1]   DIETARY PHYTOESTROGENS AND CANCER - INVITRO AND INVIVO STUDIES [J].
ADLERCREUTZ, H ;
MOUSAVI, Y ;
CLARK, J ;
HOCKERSTEDT, K ;
HAMALAINEN, E ;
WAHALA, K ;
MAKELA, T ;
HASE, T .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1992, 41 (3-8) :331-337
[2]   ISOLATION OF A NEW ESTROGEN FROM LADINO CLOVER [J].
BICKOFF, EM ;
BOOTH, AN ;
LYMAN, RL ;
LIVINGSTON, AL ;
THOMPSON, CR ;
KOHLER, GO .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1958, 6 (07) :536-539
[3]  
BLEE E, 1992, J BIOL CHEM, V267, P11881
[4]   Molecular pharmacology of aromatase and its regulation by endogenous and exogenous agents [J].
Brueggemeier, RW ;
Richards, JA ;
Joomprabutra, S ;
Bhat, AS ;
Whetstone, JL .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2001, 79 (1-5) :75-84
[5]  
CLARK JH, 1979, FEMALE SEX STEROIDS, P99
[6]   Identification of CYP2C9 as a human liver microsomal linoleic acid epoxygenase [J].
Draper, AJ ;
Hammock, BD .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2000, 376 (01) :199-205
[7]   The growth inhibitory effect of conjugated linoleic acid on MCF-7 cells is related to estrogen response system [J].
Durgam, VR ;
Fernandes, G .
CANCER LETTERS, 1997, 116 (02) :121-130
[8]  
GLASGOW W, 1990, AM SOC PHARM EXP THE, V38, P505
[9]   STRUCTURE-ACTIVITY RELATIONSHIP FOR POTENTIATION OF EGF-DEPENDENT MITOGENESIS BY OXYGENATED METABOLITES OF LINOLEIC-ACID [J].
GLASGOW, WC ;
ELING, TE .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1994, 311 (02) :286-292
[10]   CATABOLISM OF EPOXY FATTY ESTERS BY THE PURIFIED EPOXIDE HYDROLASE FROM MOUSE AND HUMAN-LIVER [J].
HALARNKAR, PP ;
WIXTROM, RN ;
SILVA, MH ;
HAMMOCK, BD .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1989, 272 (01) :226-236