Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2010-4-26
pubmed:abstractText
We report a novel PPARG germline mutation in a patient affected by colorectal cancer that replaces serine 289 with cysteine in the mature protein (S289C). The mutant has impaired transactivation potential and acts as dominant negative to the wild type receptor. In addition, it no longer restrains cell proliferation both in vitro and in vivo. Interestingly, the S289C mutant poorly activates target genes and interferes with the inflammatory pathway in tumor tissues and proximal normal mucosa. Consistently, only mutation carriers exhibit colonic lesions that can evolve to dysplastic polyps. The proband presented also dyslipidemia, hypertension and overweight, not associated to type 2 diabetes; of note, family members tested positive for the mutation and display only a dyslipidemic profile at variable penetrance with other biochemical parameters in the normal range. Finally, superimposing the mutation to the crystal structure of the ligand binding domain, the new Cys289 becomes so closely positioned to Cys285 to form an S-S bridge. This would reduce the depth of the ligand binding pocket and impede agonist positioning, explaining the biological effects and subcellular distribution of the mutant protein. This is the first PPARG germline mutation associated with dyslipidemia and colonic polyp formation that can progress to full-blown adenocarcinoma.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0006-3002
pubmed:author
pubmed:copyrightInfo
Copyright 2010 Elsevier B.V. All rights reserved.
pubmed:issnType
Print
pubmed:volume
1802
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
572-81
pubmed:meshHeading
pubmed-meshheading:20123124-Adenocarcinoma, pubmed-meshheading:20123124-Adolescent, pubmed-meshheading:20123124-Adult, pubmed-meshheading:20123124-Aged, pubmed-meshheading:20123124-Aged, 80 and over, pubmed-meshheading:20123124-Amino Acid Substitution, pubmed-meshheading:20123124-Animals, pubmed-meshheading:20123124-Base Sequence, pubmed-meshheading:20123124-Binding Sites, pubmed-meshheading:20123124-COS Cells, pubmed-meshheading:20123124-Cercopithecus aethiops, pubmed-meshheading:20123124-Colonic Neoplasms, pubmed-meshheading:20123124-DNA Primers, pubmed-meshheading:20123124-Dyslipidemias, pubmed-meshheading:20123124-Female, pubmed-meshheading:20123124-Germ-Line Mutation, pubmed-meshheading:20123124-Humans, pubmed-meshheading:20123124-Intestinal Polyps, pubmed-meshheading:20123124-Loss of Heterozygosity, pubmed-meshheading:20123124-Male, pubmed-meshheading:20123124-Mice, pubmed-meshheading:20123124-Middle Aged, pubmed-meshheading:20123124-Models, Molecular, pubmed-meshheading:20123124-NIH 3T3 Cells, pubmed-meshheading:20123124-PPAR gamma, pubmed-meshheading:20123124-Pedigree, pubmed-meshheading:20123124-Recombinant Proteins, pubmed-meshheading:20123124-Transfection, pubmed-meshheading:20123124-Young Adult
pubmed:year
2010
pubmed:articleTitle
A novel germline mutation in peroxisome proliferator-activated receptor gamma gene associated with large intestine polyp formation and dyslipidemia.
pubmed:affiliation
Department of Biological and Environmental Sciences, University of Sannio, Via Port'Arsa, 11, 82100 Benevento, Italy.
pubmed:publicationType
Journal Article, In Vitro, Case Reports, Research Support, Non-U.S. Gov't