Targeted Ablation of the WW Domain-Containing Oxidoreductase Tumor Suppressor Leads to Impaired Steroidogenesis

被引:73
作者
Aqeilan, Rami I. [1 ,2 ]
Hagan, John P.
de Bruin, Alain
Rawahneh, Maysoon
Salah, Zaidoun [2 ]
Gaudio, Eugenio
Siddiqui, Hasan
Volinia, Stefano
Alder, Hansjuerg
Lian, Jane B. [3 ,4 ]
Stein, Gary S. [3 ,4 ]
Croce, Carlo M.
机构
[1] Ohio State Univ, Human Canc Genet Program, Dept Mol Virol Immunol & Med, Ctr Comprehens Canc, Columbus, OH 43210 USA
[2] Hebrew Univ Jerusalem, Hadassah Med Sch, Inst Med Res Israel Canada, Lautenberg Ctr Gen & Tumor Immunol, IL-91120 Jerusalem, Israel
[3] Univ Massachusetts, Sch Med, Dept Cell Biol, Worcester, MA 01655 USA
[4] Univ Massachusetts, Sch Med, Ctr Canc, Worcester, MA 01655 USA
关键词
PROSTATE-CANCER; IN-VIVO; GENE; PROTEIN; EXPRESSION; IDENTIFICATION; ASSOCIATION; PROGRESSION; HORMONE; BREAST;
D O I
10.1210/en.2008-1087
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The WW domain-containing oxidoreductase ( WWOX) gene encodes a 46-kDa tumor suppressor. The Wwox protein contains two N-terminal WW domains that interact with several transcriptional activators containing proline-tyrosine motifs and a central short-chain dehydrogenase/reductase domain that has been suggested to play a role in steroid metabolism. Recently, we have shown that targeted deletion of the Wwox gene in mice leads to postnatal lethality and defects in bone growth. Here, we report that Wwox-deficient mice display impaired steroidogenesis. Mutant homozygous mice are born with gonadal abnormalities, including failure of Leydig cell development in testis and reduced theca cell proliferation in ovary. Furthermore, Wwox(-/-) mice displayed impaired gene expression of key steroidogenesis enzymes. Affymetrix microarray gene analysis revealed differentially expressed related genes in steroidogenesis in knockout mice testis and ovary as compared with control mice. These results demonstrate the essential requirement for the Wwox tumor suppressor in proper steroidogenesis. (Endocrinology 150: 1530-1535, 2009)
引用
收藏
页码:1530 / 1535
页数:6
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