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Growth differentiation factor 15 is required for triple-negative breast cancer cell growth and chemoresistance

紫杉醇 GDF15型 PI3K/AKT/mTOR通路 癌症研究 蛋白激酶B 细胞生长 三阴性乳腺癌 生物 活力测定 细胞 癌症 信号转导 乳腺癌 细胞生物学 内分泌学 生物化学 遗传学
作者
Yan‐Ling He,Xinyuan Zhang,Yunli Zhang,Wenwen Luo,Zhenyun Zhu,Kai Song,Jian Shi
出处
期刊:Anti-Cancer Drugs [Lippincott Williams & Wilkins]
被引量:1
标识
DOI:10.1097/cad.0000000000001434
摘要

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.
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