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The FGFR4-G388R Polymorphism Promotes Mitochondrial STAT3 Serine Phosphorylation to Facilitate Pituitary Growth Hormone Cell Tumorigenesis
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The FGFR4-G388R Polymorphism Promotes Mitochondrial STAT3 Serine Phosphorylation to Facilitate Pituitary Growth Hormone Cell Tumorigenesis
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Journal Article
The FGFR4-G388R Polymorphism Promotes Mitochondrial STAT3 Serine Phosphorylation to Facilitate Pituitary Growth Hormone Cell Tumorigenesis
2011
Overview
Pituitary tumors are common intracranial neoplasms, yet few germline abnormalities have been implicated in their pathogenesis. Here we show that a single nucleotide germline polymorphism (SNP) substituting an arginine (R) for glycine (G) in the FGFR4 transmembrane domain can alter pituitary cell growth and hormone production. Compared with FGFR4-G388 mammosomatotroph cells that support prolactin (PRL) production, FGFR4-R388 cells express predominantly growth hormone (GH). Growth promoting effects of FGFR4-R388 as evidenced by enhanced colony formation was ascribed to Src activation and mitochondrial serine phosphorylation of STAT3 (pS-STAT3). In contrast, diminished pY-STAT3 mediated by FGFR4-R388 relieved GH inhibition leading to hormone excess. Using a knock-in mouse model, we demonstrate the ability of FGFR4-R385 to promote GH pituitary tumorigenesis. In patients with acromegaly, pituitary tumor size correlated with hormone excess in the presence of the FGFR4-R388 but not the FGFR4-G388 allele. Our findings establish a new role for the FGFR4-G388R polymorphism in pituitary oncogenesis, providing a rationale for targeting Src and STAT3 in the personalized treatment of associated disorders.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject
/ Biology
/ Cell Transformation, Neoplastic - genetics
/ Fibroblast growth factor receptors
/ Gene Expression Regulation, Neoplastic
/ Humans
/ Kinases
/ Mice
/ Pituitary Neoplasms - genetics
/ Pituitary Neoplasms - metabolism
/ Pituitary Neoplasms - pathology
/ Polymorphism, Single Nucleotide
/ Proteins
/ Rats
/ Receptor, Fibroblast Growth Factor, Type 4 - genetics
/ Receptor, Fibroblast Growth Factor, Type 4 - metabolism
/ STAT3 Transcription Factor - genetics
/ STAT3 Transcription Factor - metabolism
/ Tumors
