Distinct allelic expression patterns of imprinted IGF2 in adenocarcinoma and squamous cell carcinoma of the lung
Author(s) -
Satoru Ozaki,
Ei Kawahara,
Shiori Maenaka,
Nguyễn Hoàng Việt,
Takeru Oyama,
Miwa Imai,
Makoto Oda,
Seiji Yano
Publication year - 2014
Publication title -
oncology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.766
H-Index - 54
eISSN - 1792-1082
pISSN - 1792-1074
DOI - 10.3892/ol.2014.2572
Subject(s) - biology , laser capture microdissection , microdissection , adenocarcinoma , imprinting (psychology) , restriction fragment length polymorphism , lung cancer , cell cycle , cancer research , oncogene , microbiology and biotechnology , polymerase chain reaction , genomic imprinting , gene , cancer , gene expression , genetics , oncology , medicine , dna methylation
The insulin-like growth factor 2 gene ( IGF2 ) is an imprinting gene, which mediates cell growth and apoptosis. The loss of imprinting (LOI) of IGF2 has been associated with the development of cancer. In the present study, loss LOI of IGF2 in lung cancer was analyzed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) in combination with DNA sequencing of samples collected by laser capture microdissection. The status of each sample was assigned as imprinting when PCR-RFLP revealed only one band or sequence with a single peak; otherwise, the case was classified as LOI. LOI was identified in eight out of 13 adenocarcinoma cases (62%), but was not detected in any of the nine squamous cell carcinoma cases (0%). These results suggest that IGF2 LOI is involved in the molecular pathogenesis of lung adenocarcinoma, but not squamous cell carcinoma, and that LOI may be detected through increased IGF2 expression levels.
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