| Literature DB >> 12169206 |
K Demopoulos1, D A Arvanitis, D A Vassilakis, N M Siafakas, D A Spandidos.
Abstract
Idiopathic pulmonary fibrosis (IPF) is a specific form of chronic interstitial pneumonia limited to the lung and characterized by a fibroproliferative response with only minor signs of inflammation, which almost always causes rapid fibrotic destruction of the lung. In this study, we investigated genomic instability in IPF, using microsatellite DNA analysis, aiming to detect any specific genetic alterations for this disease. We used 40 highly polymorphic microsatellite DNA markers, in multiplex PCR assays, to examine 52 sputum specimens from IPF patients versus correspondent venous blood. Loss of heterozygosity (LOH) was found in 20 (38.5%) patients in at least one locus. These alterations were found on markers previously associated with lung cancer located on 1p34.3, 3p21.32-p21.1, 5q32-q33.1, 9p21 and 17p13.1 where MYCL1, FHIT, SPARC, p16(Ink4) and TP53 genes have been mapped respectively. These data provide new insights into IPF pathogenesis and a new perspective for its correlation with lung cancer.Entities:
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Year: 2002 PMID： 12169206 PMCID： PMC6740283 DOI： 10.1111/j.1582-4934.2002.tb00188.x
Source DB: PubMed Journal: J Cell Mol Med ISSN： 1582-1838 Impact factor: 5.310