Efficient downregulation of ErbB-2 induces TACC1 upregulation in breast cancer cell lines

Oncol Rep. 2013 Apr;29(4):1517-23. doi: 10.3892/or.2013.2253. Epub 2013 Jan 24.

Abstract

The ErbB-2 gene, whose overexpression is observed in many types of tumors including breast cancer, plays an important role in carcinoma formation. Dysregulation of the human transforming acidic coiled-coil 1 (TACC1) and ErbB-2 genes is thought to be important in the development and progression of breast cancer. However, a putative interaction between ErbB-2 and TACC1 remains undetermined in breast cancer. After infecting BT474 cells with lentiviral-mediated ErbB2-specific shRNA, we detected the expression of ErbB-2 and TACC1 by real-time PCR and western blotting. ErbB-2 mRNA expression was decreased in the Lenti-ShERBB2 infected cells, and western blotting indicated a concordant reduction in ErbB-2 protein. TACC1 expression at the mRNA and protein levels was significantly upregulated by ErbB-2 silencing in BT474 cells. CCK-8 assay indicated that the inhibition of ErbB-2 expression increased the sensitivity of BT474 cells to docetaxel treatment. These findings provide proof and the foundation for the molecular and biological relationships of ErbB-2 and TACC1 in breast cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / pathology
  • Cell Line, Tumor
  • Docetaxel
  • Down-Regulation / drug effects
  • Female
  • Fetal Proteins / genetics*
  • Fetal Proteins / metabolism
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Microtubule-Associated Proteins / genetics*
  • Microtubule-Associated Proteins / metabolism
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism
  • Receptor, ErbB-2 / genetics*
  • Receptor, ErbB-2 / metabolism
  • Taxoids / pharmacology
  • Up-Regulation / drug effects

Substances

  • Antineoplastic Agents
  • Fetal Proteins
  • Microtubule-Associated Proteins
  • Nuclear Proteins
  • TACC1 protein, human
  • Taxoids
  • Docetaxel
  • Receptor, ErbB-2