Medical College of Wisconsin
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Genetic analysis of congenital cystic adenomatoid malformation reveals a novel pulmonary gene: fatty acid binding protein-7 (brain type). Pediatr Res 2008 Jul;64(1):11-6

Date

04/09/2008

Pubmed ID

18391847

DOI

10.1203/PDR.0b013e318174eff8

Scopus ID

2-s2.0-49849085253 (requires institutional sign-in at Scopus site)   41 Citations

Abstract

The pathogenesis of congenital cystic adenomatoid malformation (CCAM) is unknown and its natural history is unpredictable. Fatty acid binding protein-7 (FABP-7) has been previously described in brain and breast development, but never before in the lung. We investigate gene expression in CCAM, and hypothesize that CCAM results from an aberration in the signaling pathway during lung development. Under IRB approval, tissue specimens of fetal CCAM, fetal control, postnatal CCAM, and postnatal control were examined and microarray analysis was performed. Candidate differentially expressed genes were selected with log-odds ratio (B) >0 and false discovery rate <0.05. Validation of differential expression was achieved at the RNA and protein levels. FABP-7 was underexpressed in fetal CCAM compared with fetal lung in both the microarray and by RT-PCR. Findings were duplicated by Western Blot analysis and immunohistochemistry. This is the first description of FABP-7 in the human lung. Decreased expression of FABP-7 in fetal CCAM compared with normal fetal lung at both the RNA and protein levels suggests FABP-7 may have a role in pulmonary development and in the pathogenesis of CCAM.

Author List

Wagner AJ, Stumbaugh A, Tigue Z, Edmondson J, Paquet AC, Farmer DL, Hawgood S

Author

Amy Wagner MD Professor in the Surgery department at Medical College of Wisconsin




MESH terms used to index this publication - Major topics in bold

Blotting, Western
Carrier Proteins
Child
Child, Preschool
Cystic Adenomatoid Malformation of Lung, Congenital
Down-Regulation
Fatty Acid-Binding Protein 7
Female
Gene Expression Profiling
Gene Expression Regulation, Developmental
Genetic Predisposition to Disease
Gestational Age
Humans
Immunohistochemistry
Infant
Infant, Newborn
Lung
Male
Oligonucleotide Array Sequence Analysis
Reproducibility of Results
Reverse Transcriptase Polymerase Chain Reaction
Tumor Suppressor Proteins