Abstract |
WWOX ( WW domain containing oxidoreductase), a putative tumor suppressor gene that maps to the common fragile site FRA16D on chromosome 16q23.3-24.1, is altered in breast, esophageal, and ovarian cancer. Because the FRA3B/FHIT locus at 3p14.2 is a preferential target for genetic changes caused by tobacco smoke, we intended to evaluate the status of the FRA16D/WWOX gene in non-small cell lung cancer; we have analyzed 27 paired normal and tumor lung tissues and 8 lung cancer cell lines for WWOX alterations by reverse transcriptase-PCR, loss of heterozygosity, and mutation analysis. Transcripts missing WWOX exons were detected in 7 primary tumors (7 of 27; 25.9%) and 5 of 8 cell lines. In addition, loss of heterozygosity at the WWOX locus was observed in 10 primary tumors (10 of 27; 37.0%). We conclude that WWOX alterations occur in a significant fraction of lung cancers and may contribute to the pathogenesis of non-small cell lung cancer.
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Authors | Sai Yendamuri, Tamotsu Kuroki, Francesco Trapasso, Adam C Henry, Kristoffel R Dumon, Kay Huebner, Noel N Williams, Larry R Kaiser, Carlo M Croce |
Journal | Cancer research
(Cancer Res)
Vol. 63
Issue 4
Pg. 878-81
(Feb 15 2003)
ISSN: 0008-5472 [Print] United States |
PMID | 12591741
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Carrier Proteins
- Neoplasm Proteins
- RNA, Messenger
- Oxidoreductases
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Topics |
- Carcinoma, Non-Small-Cell Lung
(enzymology, genetics)
- Carrier Proteins
(biosynthesis, genetics)
- Gene Deletion
- Genes, Tumor Suppressor
- Humans
- Loss of Heterozygosity
- Lung Neoplasms
(enzymology, genetics, pathology)
- Neoplasm Proteins
(biosynthesis, genetics)
- Oxidoreductases
(biosynthesis, genetics)
- Point Mutation
- Protein Structure, Tertiary
- RNA, Messenger
(biosynthesis, genetics)
- Tumor Cells, Cultured
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