Bellio Chiara, Emperador Marta, Castellano Pol, Gris-Oliver Albert, Canals Francesc, Sánchez-Pla Alex, Zamora Esther, Arribas Joaquín, Saura Cristina, Serra Violeta, Tabernero Josep, Littlefield Bruce A, Villanueva Josep
Vall d'Hebron Institute of Oncology (VHIO), 08035 Barcelona, Spain.
Genetics Microbiology and Statistics Department, Universitat de Barcelona, 08035 Barcelona, Spain.
Cancers (Basel). 2022 May 23;14(10):2562. doi: 10.3390/cancers14102562.
Drug tolerant persister (DTP) cells enter into a reversible slow-cycling state after drug treatment. We performed proteomic characterization of the breast cancer (BC) DTP cell secretome after eribulin treatment. We showed that the growth differentiation factor 15 (GDF15) is a protein significantly over-secreted upon eribulin treatment. The biomarker potential of GDF15 was confirmed in 3D-cell culture models using BC cells lines and PDXs, as well as in a TNBC in vivo model. We also found that GDF15 is required for survival of DTP cells. Direct participation of GDF15 and its receptor GFRAL in eribulin-induction of DTPs was established by the enhanced cell killing of DTPs by eribulin seen under GDF15 and GFRAL loss of function assays. Finally, we showed that combination therapy of eribulin plus an anti-GDF15 antibody kills BC-DTP cells. Our results suggest that targeting GDF15 may help eradicate DTP cells and block the onset of acquired resistance.
药物耐受持久性(DTP)细胞在药物治疗后进入可逆的慢循环状态。我们对艾日布林治疗后的乳腺癌(BC)DTP细胞分泌组进行了蛋白质组学表征。我们发现生长分化因子15(GDF15)是艾日布林治疗后显著过度分泌的一种蛋白质。在使用BC细胞系和人源肿瘤异种移植模型(PDXs)的三维细胞培养模型以及三阴性乳腺癌(TNBC)体内模型中证实了GDF15的生物标志物潜力。我们还发现GDF15是DTP细胞存活所必需的。通过在GDF15和GFRAL功能丧失试验中观察到的艾日布林对DTP细胞的增强杀伤作用,确定了GDF15及其受体GFRAL直接参与艾日布林诱导DTPs。最后,我们表明艾日布林联合抗GDF15抗体的联合疗法可杀死BC-DTP细胞。我们的结果表明,靶向GDF15可能有助于根除DTP细胞并阻止获得性耐药的发生。