Loss of the PTCH1 gene locus in cardiac fibroma

David Scanlan, Stanley J. Radio, Marilu Nelson, Ming Zhou, Renae Streblow, Vinay Prasad, Christine Reyes, Deborah Perry, Scott Fletcher, Julia A. Bridge

Research output: Contribution to journalArticle

13 Scopus citations

Abstract

Background: Cardiac fibroma (CF) is a rare benign tumor that is poorly characterized genetically. CF is more commonly encountered in patients with Gorlin syndrome (3%) than the general population. Mutations of the tumor suppressor gene PTCH1 are the underlying cause of Gorlin syndrome. Methods: Conventional cytogenetic analysis was performed on a peripheral blood and a CF sample from a 2-week-old male. In addition, fluorescence in situ hybridization (FISH) studies were performed to assess the copy number of the PTCH1 gene locus (9q22.3) on metaphase and interphase cells from these same specimens using yeast artificial protein (YAC) probe 891G1 and on representative paraffin-embedded tissue sections of two additional CFs (one arising in a 2-month-old female and the other in a 13-week-old male). None of the patients had Gorlin syndrome. Results: Karyotypically, the following abnormal chromosomal complement was detected in the 2-week-old male's CF: 46,XY,del(9)(q22q34)[15]. FISH studies revealed homozygous loss of the PTCH1 locus in the cytogenetically analyzed CF and in the CF arising in the 13-week-old male. Heterozygous loss of this locus was identified in the remaining CF from the 2-month-old female. A mutational mechanism other than deletion may be responsible for PTCH1 inactivation on the other locus in this latter patient. Conventional cytogenetic and FISH studies of the peripheral blood sample from the 2-week-old male were normal. Conclusion: These data support a tumor suppressor gene role for PTCH1 in nonsyndromic or sporadic CFs.

Original languageEnglish (US)
Pages (from-to)93-97
Number of pages5
JournalCardiovascular Pathology
Volume17
Issue number2
DOIs
StatePublished - Mar 2008

Keywords

  • Cardiac fibroma
  • Gorlin syndrome
  • PTCH1 gene

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Cardiology and Cardiovascular Medicine

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    Scanlan, D., Radio, S. J., Nelson, M., Zhou, M., Streblow, R., Prasad, V., Reyes, C., Perry, D., Fletcher, S., & Bridge, J. A. (2008). Loss of the PTCH1 gene locus in cardiac fibroma. Cardiovascular Pathology, 17(2), 93-97. https://doi.org/10.1016/j.carpath.2007.08.001