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Published in: Clinical Orthopaedics and Related Research® 9/2008

01-09-2008 | Symposium: Molecular Genetics in Sarcoma

PATCHED-ONE or SMOOTHENED Gene Mutations Are Infrequent in Chondrosarcoma

Authors: Taiqiang Yan, MD, Mark Angelini, MD, FRCSC, Benjamin A. Alman, MD, FRCSC, Irene L. Andrulis, PhD, Jay S. Wunder, MD, MSc, FRCS(C)

Published in: Clinical Orthopaedics and Related Research® | Issue 9/2008

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Excerpt

Constitutive hedgehog signaling has been implicated in the tumorigenesis of cartilaginous neoplasia; however, a common mutational mechanism remains unknown. Some tumors exhibiting hedgehog pathway activation such as basal cell cancer frequently harbor PATCHED-ONE (PTCH-1) or SMOOTHENED (SMO) gene mutations. We therefore asked whether mutations of the hedgehog receptor genes PTCH-1 or SMO occur in cartilage tumors. Single-strand conformation polymorphism (SSCP) analysis with subsequent manual sequencing was performed to detect alterations of PTCH-1 and SMO in 46 cartilage tumors. SSCP detected five shifts in the PTCH-1 gene and two shifts in SMO. Direct DNA sequencing revealed the five shifts in PTCH-1 were caused by silent nucleotide alterations. The two SMO shifts were the result of the same missense mutation (783G>A) and occurred in one dedifferentiated chondrosarcoma and a synovial chondromatosis. The patient with chondromatosis also carried this same mutation in the germline. However, this mutation was also identified in leukocyte DNA from three of 127 (2.4%) control subjects without cartilage tumors, suggesting it may represent a rare SMO variant. Constitutive activation of the hedgehog signaling pathway in chondrosarcoma is rarely caused by PTCH-1 or SMO mutations. …
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Metadata
Title
PATCHED-ONE or SMOOTHENED Gene Mutations Are Infrequent in Chondrosarcoma
Authors
Taiqiang Yan, MD
Mark Angelini, MD, FRCSC
Benjamin A. Alman, MD, FRCSC
Irene L. Andrulis, PhD
Jay S. Wunder, MD, MSc, FRCS(C)
Publication date
01-09-2008
Publisher
Springer-Verlag
Published in
Clinical Orthopaedics and Related Research® / Issue 9/2008
Print ISSN: 0009-921X
Electronic ISSN: 1528-1132
DOI
https://doi.org/10.1007/s11999-008-0332-2

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