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[Involvement of epidermal growth factor receptor signaling pathway in tamoxifen resistance of MCF-7 cells]
Lin-Lin Zhen1, Xun Zhu, Wei Zheng
1Department of General Surgery, The First Affiliated Hospital, Nanjing Medical University, Nanjing, Jiangsu, 210029, P. R. China.
Background & Objective:
Tamoxifen (TAM) is an important endocrine therapeutic drug used in combined treatment for breast cancer. However the drug resistant effect of TAM has become a major concern in clinical use. Epidermal growth factor receptor (EGFR) is expressed in many tumors and the expression of EGFR in breast cancer tissues is associated with poor prognosis. This study was to investigate EGFR signaling pathway in the drug resistant effect of TAM in breast cancer cells.
Methods:
An estrogen receptor (ER) positive breast cancer cell line, MCF-7 was incubated with TAM (10(-7) mol/L) for up to 6 months to produce drug resistant cells. mRNA and protein expression of EGFR signaling pathway related genes and ER gene was analyzed by fluorescent quantitation reverse transcription-polymerase chain reaction (fqRT-PCR) and Western blot. AG1478, an EGFR inhibitor, was also used to study the drug resistant effect of TAM.
Results:
The proliferation of MCF-7 cells was inhibited in the early stage after TAM treatment. However the inhibitory effect vanished after continuous 6-month treatment and the cell proliferation rate returned back to normal. The tolerance of MCF-7 cells to TAM was confirmed by cell growth inhibitory test. In TAM resistant MCF-7 cells, the expression of EGFR mRNA was increased by 4.5 times and the protein expression of EGFR, phosphorylation-extracellular signal-regulated kinase (p-ERK1/2) was also increased dramatically (P<0.05). While ER protein expression remained unchanged. Moreover the drug resistant cells were identified more sensitive to AG1478.
Conclusion:
In endocrine therapy, TAM resistant breast cancer cells are likely to be generated by the activation of EGFR signaling pathway after long-term TAM treatment, and EGFR inhibitors might increase the therapeutic effects in breast cancer treatment.
Insights
Tamoxifen resistance in breast cancer cells develops through the activation of the epidermal growth factor receptor (EGFR) signaling pathway. Targeting EGFR with inhibitors may improve tamoxifen treatment efficacy.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Tamoxifen (TAM) is a key endocrine therapy for breast cancer.
- Drug resistance to TAM is a significant clinical challenge.
- Epidermal growth factor receptor (EGFR) expression correlates with poor prognosis in breast cancer.
Purpose of the Study:
- To investigate the role of the EGFR signaling pathway in tamoxifen (TAM) drug resistance in breast cancer cells.
- To understand the mechanisms underlying TAM resistance.
- To explore potential therapeutic strategies targeting EGFR.
Main Methods:
- Developed TAM-resistant MCF-7 breast cancer cells through prolonged exposure.
- Analyzed gene and protein expression of EGFR signaling pathway components using fqRT-PCR and Western blot.
- Utilized an EGFR inhibitor (AG1478) to assess its effect on TAM-resistant cells.
Main Results:
- Prolonged TAM treatment led to acquired resistance in MCF-7 cells.
- TAM-resistant cells showed significantly increased EGFR mRNA and protein expression.
- Elevated levels of phosphorylated ERK1/2 (p-ERK1/2) were observed in resistant cells.
- Estrogen receptor (ER) protein levels remained unchanged.
- TAM-resistant cells exhibited increased sensitivity to the EGFR inhibitor AG1478.
Conclusions:
- Activation of the EGFR signaling pathway is implicated in the development of TAM resistance in breast cancer.
- EGFR inhibitors show potential to enhance therapeutic outcomes in TAM-resistant breast cancer.
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