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Updated: Aug 12, 2025

Isolation and Functional Assessment of Human Breast Cancer Stem Cells from Cell and Tissue Samples
Published on: October 2, 2020
Growth differentiation factor 15 is required for triple-negative breast cancer cell growth and chemoresistance
Yanling He1, Xinyuan Zhang, Yunli Zhang
1Department of Pathology, School of Basic Medical Science, Southern Medical University, Guangzhou, China.
Abstract:
Growth differentiation factor 15 (GDF15) is a pleiotropic cytokine, which is involved in the cellular stress response following acute damage. However, the functional role of GDF15 in triple-negative breast cancer (TNBC) has not been fully elucidated. ELISA, Western blot, and PCR assays as well as bioinformatics analyses were conducted to observe the expression of GDF15. Cell Counting Kit-8, 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and crystal violet staining assays were conducted to evaluate paclitaxel resistance and cell viability. Cell apoptosis was analyzed by Western blotting. Murine xenograft model assay was employed to evaluate tumor growth in vivo . Our data indicate that GDF15 is markedly elevated in paclitaxel-resistant TNBC cells, which is significantly associated with unfavorable prognosis. Silencing of GDF15 robustly inhibits the proliferation of tumor cells and increases their sensitivity to paclitaxel in vitro and in vivo , whereas the treatment of purified GDF15 protein confers breast cancer cells with chemoresistance ability. Moreover, GDF15 activates protein kinase B (AKT) /mammalian target of rapamycin (mTOR) signaling, inhibition of AKT or mTOR reverses the prosurvival effect of GDF15 and enhances the antitumor efficacy of paclitaxel in TNBC cells. Altogether, our study uncovers the role of GDF15 in tumor growth and paclitaxel resistance, implicating a potential therapeutic target for TNBC.
Insights
Growth Differentiation Factor 15 (GDF15) promotes paclitaxel resistance in triple-negative breast cancer (TNBC). Inhibiting GDF15 or its downstream AKT/mTOR pathway enhances chemotherapy sensitivity and reduces tumor growth.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Growth Differentiation Factor 15 (GDF15) is a cytokine involved in cellular stress responses.
- The specific role of GDF15 in triple-negative breast cancer (TNBC) and its impact on chemotherapy resistance remain unclear.
Purpose of the Study:
- To investigate the functional role of GDF15 in TNBC proliferation and paclitaxel resistance.
- To explore the underlying molecular mechanisms, including the AKT/mTOR signaling pathway.
Main Methods:
- Expression analysis using ELISA, Western blot, and PCR.
- Assessment of cell viability, proliferation, and apoptosis via CCK-8, MTT, and crystal violet assays.
- In vivo evaluation using a murine xenograft model and mechanistic studies involving AKT/mTOR inhibition.
Main Results:
- GDF15 expression is significantly elevated in paclitaxel-resistant TNBC cells and correlates with poor prognosis.
- GDF15 silencing decreased tumor cell proliferation and enhanced paclitaxel sensitivity in vitro and in vivo.
- GDF15 treatment conferred chemoresistance, mediated by the activation of the AKT/mTOR signaling pathway.
Conclusions:
- GDF15 plays a critical role in promoting tumor growth and paclitaxel resistance in TNBC.
- Targeting GDF15 or the AKT/mTOR pathway represents a potential therapeutic strategy for overcoming chemoresistance in TNBC.
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