Exp Mol Med.  2001 Mar;33(1):29-31.

F508 amino acid deletion mutation of CFTR gene in Korean lung cancer patients

Affiliations
  • 1Department of Biochemistry and Institute of Basic Medical Science, Wonju College of Medicine, Yonsei University, Korea.

Abstract

Mutations of the transmembrane conductance regulator (CFTR) gene in cystic fibrosis lead to dysfunction of the lung, pancreas, and sweat glands, etc. To investigate the possibility of the relationship between lung cancer and the mutations of CFTR gene, we determined amino acid sequences using reverse transcription-polymerase chain reaction (RT-PCR) and DNA sequencing. In this study, the deletion mutation of 508th amino acid in one of nine lung caner patients was found confirming that CFTR gene mutation exists in a Korean lung cancer patient.

Keyword

CFTR; mutation; lung cancer

MeSH Terms

Adult
Aged
Cystic Fibrosis Transmembrane Conductance Regulator/*genetics
Female
Human
Korea
Lung Neoplasms/*genetics
Male
Middle Age
*Sequence Deletion
Support, Non-U.S. Gov't
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