Loss-of-function mutations in PPARγ associated with human colon cancer

被引:449
作者
Sarraf, P
Mueller, E
Smith, WM
Wright, HM
Kum, JB
Aaltonen, LA
de la Chapelle, A
Spiegelman, BM
Eng, C [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Cell Biol, Dana Farber Canc Inst,Dept Canc Biol, Boston, MA 02115 USA
[2] Ohio State Univ, Ctr Comprehens Canc, Human Canc Genet Program, Columbus, OH 43210 USA
[3] Univ Helsinki, Haartman Inst, Dept Med Genet, FIN-00014 Helsinki, Finland
关键词
D O I
10.1016/S1097-2765(01)80012-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The gamma isoform of the peroxisome proliferator-activated receptor, PPAR gamma, regulates adipocyte differentiation and has recently been shown to be expressed in neoplasia of the colon and other tissues. We have found four somatic PPAR gamma mutations among 55 sporadic coln cancers: one nonsense, one frameshift, and two missense mutations. Each greatly impaired the function of the protein. c.472delA results in deletion of the entire ligand binding domain. Q286P and K319X retain a total or partial ligand binding domain but lose the ability to activate transcription through a failure to bind to ligands. R288H showed a normal response to synthetic ligands but greatly decreased transcription and binding when exposed to natural ligands. These data indicate that colon cancer in humans is associated with loss-of-function mutations in PPAR gamma.
引用
收藏
页码:799 / 804
页数:6
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