Breast cancer. Cyr61 is overexpressed, estrogen-inducible, and associated with more advanced disease

J Biol Chem. 2001 Apr 27;276(17):14187-94. doi: 10.1074/jbc.M009755200. Epub 2001 Jan 31.

Abstract

To identify genes involved in breast cancer, polymerase chain reaction-selected cDNA subtraction was utilized to construct a breast cancer-subtracted library. Differential screening of the library isolated the growth factor-inducible immediate-early gene Cyr61, a secreted, cysteine-rich, heparin binding protein that promotes endothelial cell adhesion, migration, and neovascularization. Northern analysis revealed that Cyr61 was expressed highly in the invasive breast cancer cell lines MDA-MB-231, T47D, and MDA-MB-157; very low levels were found in the less tumorigenic MCF-7 and BT-20 breast cancer cells and barely detectable amounts were expressed in the normal breast cells, MCF-12A. Univariate analysis showed a significant or borderline significant association between Cyr61 expression and stage, tumor size, lymph node positivity, age, and estrogen receptor levels. Interestingly, expression of Cyr61 mRNA increased 8- to 12-fold in MCF-12A and 3- to 5-fold in MCF-7 cells after 24- and 48-h exposure to estrogen, respectively. Induction of Cyr61 mRNA was blocked by tamoxifen and ICI182,780, inhibitors of the estrogen receptor. Stable expression of Cyr61 cDNA under the regulation of a constitutive promoter in MCF-7 cells enhanced anchorage-independent cell growth in soft agar and significantly increased tumorigenicity and vascularization of these tumors in nude mice. Moreover, overexpression of Cyr61 in MCF-12A normal breast cells induced their tumor formation and vascularization in nude mice. In summary, these results suggest that Cyr61 may play a role in the progression of breast cancer and may be involved in estrogen-mediated tumor development.

Publication types

  • 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

  • Adult
  • Age Factors
  • Aged
  • Aged, 80 and over
  • Animals
  • Antineoplastic Agents, Hormonal / pharmacology
  • Blotting, Northern
  • Breast Neoplasms / blood supply
  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / metabolism*
  • Carcinoma, Ductal, Breast / metabolism
  • Carcinoma, Ductal, Breast / pathology
  • Cell Movement
  • Cells, Cultured
  • Cysteine-Rich Protein 61
  • DNA, Complementary / metabolism
  • Disease Progression
  • Estradiol / analogs & derivatives*
  • Estradiol / pharmacology
  • Estrogen Antagonists / pharmacology
  • Estrogens / metabolism*
  • Female
  • Fulvestrant
  • Gene Library
  • Growth Substances / biosynthesis*
  • Humans
  • Immediate-Early Proteins / biosynthesis*
  • Intercellular Signaling Peptides and Proteins*
  • Mice
  • Mice, Nude
  • Middle Aged
  • Multivariate Analysis
  • Neoplasm Transplantation
  • Promoter Regions, Genetic
  • Protein Binding
  • Receptors, Estrogen / biosynthesis
  • Recombinant Proteins / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tamoxifen / pharmacology
  • Time Factors
  • Transfection
  • Tumor Cells, Cultured

Substances

  • Antineoplastic Agents, Hormonal
  • CCN1 protein, human
  • CCN1 protein, mouse
  • Cysteine-Rich Protein 61
  • DNA, Complementary
  • Estrogen Antagonists
  • Estrogens
  • Growth Substances
  • Immediate-Early Proteins
  • Intercellular Signaling Peptides and Proteins
  • Receptors, Estrogen
  • Recombinant Proteins
  • Tamoxifen
  • Fulvestrant
  • Estradiol