Identification of genes differentially expressed in normal lung and non-small cell lung carcinoma tissue

Cancer Res. 1994 Oct 1;54(19):5236-40.

Abstract

Using a magnet-assisted subtraction technique, 17 complementary DNA (cDNA) clones were isolated that were expressed in the normal lung but were decreased or lost in the corresponding tumor tissue of a nonsmall cell lung carcinoma patient. The lack of expression of six magnet-assisted subtraction technique cDNA clones in three additional non-small cell lung carcinoma cases indicates their possible relevance for non-small cell lung carcinoma. Two cDNA clones revealed homology to genes specifically expressed in lung, i.e., pulmonary surfactant-associated protein B and the receptor for advanced glycosylation end products of proteins. Three cDNA clones showed identity to cDNA sequences encoding calmodulin-like protein, glutamine synthetase, and cytoskeletal beta-actin. One cDNA clone is identical to a recently described human expressed sequence tag whose gene is still unknown.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Calcium-Binding Proteins / genetics
  • Carcinoma, Non-Small-Cell Lung / genetics*
  • DNA, Complementary / isolation & purification*
  • Extracellular Matrix Proteins
  • Gene Expression Regulation, Neoplastic*
  • Glycoproteins / genetics
  • Humans
  • Lung / metabolism*
  • Lung Neoplasms / genetics*
  • Molecular Sequence Data
  • Proteolipids / genetics
  • Pulmonary Surfactants / genetics
  • Receptor for Advanced Glycation End Products
  • Receptors, Immunologic / genetics
  • Subtraction Technique

Substances

  • Calcium-Binding Proteins
  • DNA, Complementary
  • Extracellular Matrix Proteins
  • Glycoproteins
  • Proteolipids
  • Pulmonary Surfactants
  • Receptor for Advanced Glycation End Products
  • Receptors, Immunologic
  • SPARCL1 protein, human

Associated data

  • GENBANK/S73397