Molecular characterization of the human δ opioid receptor in lung cancer

Published

Journal Article

A variety of neuropeptide receptors have been detected in human lung cancer. They are thought to play a role in autocrin/paracrine regulation of cell growth, and may be clinically useful a diagnostic, prognostic or therapeutic targets. The current study characterizes the molecular structure of the δ opioid receptor and its gene expression level in lung cancer cell lines relative to normal human lung using a sensitive RT-PCR approach. The goals of this investigation were a) to define the correlation between receptor binding and gene expression in lung cancer cell lines, and b) to determine the cDNA sequence integrity of this receptor in comparison the the receptor recently found in human brain. Five small cell lung cancer (SCLC) cell lines revealed size-matched RT-PCR products which strongly hybridized to the human brain δ opioid receptor probe. One of three non-small cell lung cancer (NSCLC) cell lines (NCI-H23), known to be negative by binding analysis, demonstrated low level expression. No gene expression was found in normal human lung. RT-PCR products from two level expressing NSCLC cell line (NCI-23) were subjected to bidirectional DNA sequence analysis and the receptor ends were resolved using a 3'-end RACE and 5'-end gene-specific approach. The isolated cDNA sequences proved to be identical to the published human brain δ opioid receptor sequence. These data show that lung cancers with neuroendocrine features express human brain δ opioid receptors in contrast to normal lung, and that the δ opioid receptor mRNA in lung cancer is not mutated. This unique feature of lung cancer may be exploitable for diagnostic, prognostic, and therapeutic strategies.

Duke Authors

Cited Authors

  • Schreiber, G; Campa, MJ; Prabhakar, S; O'Briant, K; Bepler, G; Patz, EF

Published Date

  • May 1, 1998

Published In

Volume / Issue

  • 18 / 3 A

Start / End Page

  • 1787 - 1792

International Standard Serial Number (ISSN)

  • 0250-7005

Citation Source

  • Scopus