Literature DB >> 10529789

New perspectives on the molecular basis of hereditary bone tumours.

C McCormick1, G Duncan, F Tufaro.   

Abstract

Bone development is a highly regulated process sensitive to a wide variety of hormones, inflammatory mediators and growth factors. One of the most common hereditary skeletal dysplasias, hereditary multiple exostoses (HME), is an autosomal dominant disorder characterized by skeletal malformations that manifest as bony, benign tumours near the end of long bones. HME is usually caused by defects in either one of two genes, EXT1 and EXT2, which encode enzymes that catalyse the biosynthesis of heparan sulphate, an important component of the extracellular matrix. Thus, HME-linked bone tumours, like many other skeletal dysplasias, probably result from disruptions in cell surface architecture. However, despite the recent success in unravelling functions for several members of the EXT gene family, significant challenges remain before this knowledge can be used to develop new approaches for the diagnosis and treatment of disease.

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Year:  1999        PMID: 10529789     DOI: 10.1016/s1357-4310(99)01593-2

Source DB:  PubMed          Journal:  Mol Med Today        ISSN: 1357-4310


  7 in total

Review 1.  Order and disorder: the role of extracellular matrix in epithelial cancer.

Authors:  Derek Radisky; John Muschler; Mina J Bissell
Journal:  Cancer Invest       Date:  2002       Impact factor: 2.176

2.  Osteochondroma causing diaphragmatic rupture and bowel obstruction in a 14-year-old boy.

Authors:  Fizan Abdullah; Robert Kanard; Dominic Femino; Henri Ford; James Stein
Journal:  Pediatr Surg Int       Date:  2006-01-03       Impact factor: 1.827

3.  High quality RNA isolation from tumours with low cellularity and high extracellular matrix component for cDNA microarrays: application to chondrosarcoma.

Authors:  H J Baelde; A M Cleton-Jansen; H van Beerendonk; M Namba; J V Bovée; P C Hogendoorn
Journal:  J Clin Pathol       Date:  2001-10       Impact factor: 3.411

4.  A Genotype-Phenotype Study of Multiple Hereditary Exostoses in Forty-Three Patients.

Authors:  Sungmin Kim; Chang-Hyun Lee; Seok-Yong Choi; Myeong-Kyu Kim; Sung Taek Jung
Journal:  J Clin Med       Date:  2022-06-27       Impact factor: 4.964

5.  Hereditary multiple exostoses: A case report and literature review.

Authors:  Thi Hien Ha; Thi Minh Thi Ha; Mao Nguyen Van; Trong Binh Le; Nghi Thanh Nhan Le; Thao Nguyen Thanh; Dac Hong An Ngo
Journal:  SAGE Open Med Case Rep       Date:  2022-06-07

6.  Multiple osteochondromas: clinicopathological and genetic spectrum and suggestions for clinical management.

Authors:  Liesbeth Hameetman; Judith Vmg Bovée; Antonie Hm Taminiau; Herman M Kroon; Pancras Cw Hogendoorn
Journal:  Hered Cancer Clin Pract       Date:  2004-11-15       Impact factor: 2.857

7.  Osteochondroma: ignore or investigate?

Authors:  Antônio Marcelo Gonçalves de Souza; Rosalvo Zósimo Bispo Júnior
Journal:  Rev Bras Ortop       Date:  2014-10-27
  7 in total

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