Differential screening and suppression subtractive hybridization identified genes differentially expressed in an estrogen receptor-positive breast carcinoma cell line

Nucleic Acids Res. 1998 Feb 15;26(4):1116-23. doi: 10.1093/nar/26.4.1116.

Abstract

Differences in gene expression are likely to explain the phenotypic differences between hormone-responsive and hormone-unresponsive breast cancer. We have identified differentially expressed cDNAs in the estrogen receptor (ER)-positive MCF7 breast carcinoma cell line compared with the ER-negative MDA-MB-231 breast carcinoma cell line. Differential screening isolated four differentially expressed genes: cytokeratin 8, cytokeratin 18, Hsp27 and GPCR -Br. To identify differentially expressed genes of lower abundance, suppression subtractive hybridization was utilized and 29 differentially expressed clones were isolated. Sequence analysis revealed that 11 clones were from previously described genes: HEK8, neuropeptide Y receptor Y1, p21 WAF-1, p55 PIK, cytokeratin 18 (cloned twice), fructose-1,6-biphosphatase, cytokeratin 8, TGFbeta1 binding protein, elongation factor 1alpha2 and pS2. The remaining 18 clones did not match sequences in the GenBank/EMBL database, indicating that they may be novel genes. Expression of pS2, neuropeptide Y receptor Y1 and three novel clones was induced by estradiol, indicating estrogen-responsiveness. The expression pattern of one novel gene, DEME -6, correlated with expression of ER and ERF -1/ AP -2gamma in a panel of breast carcinoma cell lines. A 2.6 kb cDNA of DEME -6 was sequenced and contains an open reading frame of 574 amino acids that demonstrates 62.4% similarity with a gene from Caenorhabditis elegans chromosome III. Expression of DEME -6 was also detected in primary breast carcinomas but not in normal breast tissue, as determined by RT-PCR. These findings support the hypothesis that a set of genes coordinately regulated with ER , but not necessarily estradiol-responsive, are characteristic of the hormone-responsive breast cancer phenotype.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / metabolism*
  • DNA Primers / genetics
  • DNA, Complementary / genetics
  • DNA, Neoplasm / genetics
  • Female
  • Gene Expression
  • Humans
  • Molecular Sequence Data
  • Neoplasm Proteins / genetics*
  • Neoplasms, Hormone-Dependent / genetics*
  • Neoplasms, Hormone-Dependent / metabolism*
  • Nucleic Acid Hybridization
  • Oncogenes*
  • Phenotype
  • Receptors, Estrogen / genetics
  • Receptors, Estrogen / metabolism*
  • Tumor Cells, Cultured

Substances

  • DNA Primers
  • DNA, Complementary
  • DNA, Neoplasm
  • Neoplasm Proteins
  • Receptors, Estrogen
  • TTC39A protein, human

Associated data

  • GENBANK/AA506763
  • GENBANK/AA506764
  • GENBANK/AA506765
  • GENBANK/AA506766
  • GENBANK/AA506767
  • GENBANK/AA506768
  • GENBANK/AA506769
  • GENBANK/AA506770
  • GENBANK/AA506771
  • GENBANK/AA506772
  • GENBANK/AA506773
  • GENBANK/AA506774
  • GENBANK/AA506775
  • GENBANK/AA506776
  • GENBANK/AA506777
  • GENBANK/AA506778
  • GENBANK/AA506779
  • GENBANK/AA506780
  • GENBANK/AA506781
  • GENBANK/AA506782
  • GENBANK/AA506783
  • GENBANK/AA506784
  • GENBANK/AA506785
  • GENBANK/AA506786
  • GENBANK/AA506787
  • GENBANK/AA506788
  • GENBANK/AA506789
  • GENBANK/AA506790
  • GENBANK/AA506791
  • GENBANK/AA506792