Literature DB >> 10646121

Mutations of the GNAS1 gene, stromal cell dysfunction, and osteomalacic changes in non-McCune-Albright fibrous dysplasia of bone.

P Bianco1, M Riminucci, A Majolagbe, S A Kuznetsov, M T Collins, M H Mankani, A Corsi, H G Bone, S Wientroub, A M Spiegel, L W Fisher, P G Robey.   

Abstract

Activating missense mutations of the GNAS1 gene, encoding the alpha subunit of the stimulatory G protein (Gs), have been identified in patients with the McCune-Albright syndrome (MAS; characterized by polyostotic fibrous dysplasia, café au lait skin pigmentation, and endocrine disorders). Because fibrous dysplasia (FD) of bone also commonly occurs outside of the context of typical MAS, we asked whether the same mutations could be identified routinely in non-MAS FD lesions. We analyzed a series of 8 randomly obtained, consecutive cases of non-MAS FD and identified R201 mutations in the GNAS1 gene in all of them by sequencing cDNA generated by amplification of genomic DNA using a standard primer set and by using a novel, highly sensitive method that uses a protein nucleic acid (PNA) primer to block amplification of the normal allele. Histologic findings were not distinguishable from those observed in MAS-related FD and included subtle changes in cell shape and collagen texture putatively ascribed to excess endogenous cyclic adenosine monophosphate (cAMP). Osteomalacic changes (unmineralized osteoid) were prominent in lesional FD bone. In an in vivo transplantation assay, stromal cells isolated from FD failed to recapitulate a normal ossicle; instead, they generated a miniature replica of fibrous dysplasia. These data provide evidence that occurrence of GNAS1 mutations, previously noted in individual cases of FD, is a common and perhaps constant finding in non-MAS FD. These findings support the view that FD, MAS, and nonskeletal isolated endocrine lesions associated with GNAS1 mutations represent a spectrum of phenotypic expressions (likely reflecting different patterns of somatic mosaicism) of the same basic disorder. We conclude that mechanisms underlying the development of the FD lesions, and hopefully mechanism-targeted therapeutic approaches to be developed, must also be the same in MAS and non-MAS FD.

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Year:  2000        PMID: 10646121     DOI: 10.1359/jbmr.2000.15.1.120

Source DB:  PubMed          Journal:  J Bone Miner Res        ISSN: 0884-0431            Impact factor:   6.741


  57 in total

1.  Fibrocartilaginous dysplasia (fibrous dysplasia with extensive cartilaginous differentiation).

Authors:  Roberto Vargas-Gonzalez; Sergio Sanchez-Sosa
Journal:  Pathol Oncol Res       Date:  2006-06-24       Impact factor: 3.201

2.  The role of type 1 and type 2 5'-deiodinase in the pathophysiology of the 3,5,3'-triiodothyronine toxicosis of McCune-Albright syndrome.

Authors:  Francesco S Celi; Giuseppe Coppotelli; Aaron Chidakel; Marilyn Kelly; Beth A Brillante; Thomas Shawker; Natasha Cherman; Penelope P Feuillan; Michael T Collins
Journal:  J Clin Endocrinol Metab       Date:  2008-03-18       Impact factor: 5.958

Review 3.  Carney complex and McCune Albright syndrome: an overview of clinical manifestations and human molecular genetics.

Authors:  Paraskevi Salpea; Constantine A Stratakis
Journal:  Mol Cell Endocrinol       Date:  2013-09-05       Impact factor: 4.102

4.  Analysis of GNAS mutations in cemento-ossifying fibromas and cemento-osseous dysplasias of the jaws.

Authors:  Milan M Patel; Jonathan F Wilkey; Rafik Abdelsayed; Nisha J D'Silva; Carl Malchoff; Sanjay M Mallya
Journal:  Oral Surg Oral Med Oral Pathol Oral Radiol Endod       Date:  2010-03-25

5.  Endoscopic Endonasal Optic Nerve Decompression for Fibrous Dysplasia.

Authors:  Timothy R DeKlotz; S Tonya Stefko; Juan C Fernandez-Miranda; Paul A Gardner; Carl H Snyderman; Eric W Wang
Journal:  J Neurol Surg B Skull Base       Date:  2016-06-02

6.  Fibrocartilaginous intramedullary bone forming tumor of the distal femur mimicking osteosarcoma.

Authors:  Sang-Heon Song; Hanna Lee; Hae-Ryong Song; Myo-Jong Kim; Jong-Hoon Park
Journal:  J Korean Med Sci       Date:  2013-03-27       Impact factor: 2.153

Review 7.  Fibrous dysplasia and fibroblast growth factor-23 regulation.

Authors:  Alison M Boyce; Nisan Bhattacharyya; Michael T Collins
Journal:  Curr Osteoporos Rep       Date:  2013-06       Impact factor: 5.096

8.  GNAS Mutations in Fibrous Dysplasia: A Comparative Study of Standard Sequencing and Locked Nucleic Acid PCR Sequencing on Decalcified and Nondecalcified Formalin-fixed Paraffin-embedded Tissues.

Authors:  George Jour; Alifya Oultache; Justyna Sadowska; Talia Mitchell; John Healey; Khedoudja Nafa; Meera Hameed
Journal:  Appl Immunohistochem Mol Morphol       Date:  2016-10

9.  Sinonasal disease in polyostotic fibrous dysplasia and McCune-Albright Syndrome.

Authors:  Timothy R DeKlotz; Hung Jeffrey Kim; Marilyn Kelly; Michael T Collins
Journal:  Laryngoscope       Date:  2013-02-26       Impact factor: 3.325

Review 10.  Molecular pathology of sarcomas: concepts and clinical implications.

Authors:  Judith V M G Bovée; Pancras C W Hogendoorn
Journal:  Virchows Arch       Date:  2009-09-29       Impact factor: 4.064

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