Targeting ABCA12-controlled ceramide homeostasis inhibits breast cancer stem cell function and chemoresistance

• Published in: Science advances Vol. 9; no. 48; p. eadh1891
• Main Authors: Cui, Jihong, Christin, John R, Reisz, Julie A, Cendali, Francesca Isabelle, Sanawar, Rahul, Coutinho De Miranda, Marcelo, D'Alessandro, Angelo, Guo, Wenjun
• Format: Journal Article
• Language: English
• Published: United States 01.12.2023
• Subjects: ATP-Binding Cassette Transporters - genetics; ATP-Binding Cassette Transporters - metabolism; Breast Neoplasms - metabolism; Cell Line, Tumor; Drug Resistance, Neoplasm; Female; Homeostasis; Humans; Lipids; Neoplastic Stem Cells - metabolism
• ISSN: 2375-2548; 2375-2548
• DOI: 10.1126/sciadv.adh1891

Cancer stem cells (CSCs) drive tumor growth, metastasis, and chemoresistance. While emerging evidence suggests that CSCs have a unique dependency on lipid metabolism, the functions and regulation of distinct lipid species in CSCs remain poorly understood. Here, we developed a stem cell factor SOX9-based reporter for isolating CSCs in primary tumors and metastases of spontaneous mammary tumor models. Transcriptomic analyses uncover that SOX9 CSCs up-regulate the ABCA12 lipid transporter. ABCA12 down-regulation impairs cancer stemness and chemoresistance. Lipidomic analyses reveal that ABCA12 maintains cancer stemness and chemoresistance by reducing intracellular ceramide abundance, identifying a CSC-associated function of ABCA subfamily transporter. Ceramide suppresses cancer stemness by inhibiting the YAP-SOX9 signaling pathway in CSCs. Increasing ceramide levels in tumors enhances their sensitivity to chemotherapy and prevents the enrichment of SOX9 CSCs. In addition, SOX9 and ABCA12 cancer cells contribute to chemoresistance in human patient-derived xenografts. These findings identify a CSC-suppressing lipid metabolism pathway that can be exploited to inhibit CSCs and overcome chemoresistance.