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Updated: May 14, 2026

Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
Efficient downregulation of ErbB-2 induces TACC1 upregulation in breast cancer cell lines
Jinyu Xiang1, Wensheng Qiu, Xingang Wang
1Department of Oncology, The Affiliated Hospital of the Medical College, Qingdao University, Qingdao 266003, PR China.
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.
Insights
Overexpressing ErbB-2 in breast cancer is linked to TACC1. Silencing ErbB-2 increases TACC1 and enhances docetaxel sensitivity in breast cancer cells.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- ErbB-2 overexpression is common in breast cancer, contributing to carcinoma formation.
- Dysregulation of transforming acidic coiled-coil 1 (TACC1) and ErbB-2 is implicated in breast cancer development and progression.
- The interaction between ErbB-2 and TACC1 in breast cancer remains unclear.
Purpose of the Study:
- To investigate the molecular relationship between ErbB-2 and TACC1 in breast cancer.
- To determine the effect of ErbB-2 silencing on TACC1 expression.
- To assess the impact of ErbB-2 inhibition on breast cancer cell sensitivity to docetaxel.
Main Methods:
- Utilized lentiviral-mediated ErbB2-specific shRNA to infect BT474 cells.
- Quantified ErbB-2 and TACC1 expression using real-time PCR and western blotting.
- Assessed cell proliferation and drug sensitivity via CCK-8 assay.
Main Results:
- ErbB-2 silencing significantly reduced ErbB-2 mRNA and protein levels in BT474 cells.
- TACC1 expression, at both mRNA and protein levels, was significantly upregulated following ErbB-2 silencing.
- Inhibition of ErbB-2 expression enhanced the sensitivity of BT474 cells to docetaxel treatment.
Conclusions:
- Demonstrated a significant upregulation of TACC1 expression upon ErbB-2 silencing in breast cancer cells.
- Provided evidence for a molecular and biological relationship between ErbB-2 and TACC1 in breast cancer.
- Established that inhibiting ErbB-2 expression can increase breast cancer cell sensitivity to docetaxel, suggesting therapeutic potential.
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