Adipocyte lipolysis links obesity to breast cancer growth: adipocyte-derived fatty acids drive breast cancer cell proliferation and migration. Issue 1 (December 2017)

• Record Type: Journal Article
• Authors: Balaban, Seher; Shearer, Robert; Lee, Lisa; van Geldermalsen, Michelle; Schreuder, Mark; Shtein, Harrison; Cairns, Rose; Thomas, Kristen; Fazakerley, Daniel; Grewal, Thomas; Holst, Jeff; Saunders, Darren; Hoy, Andrew
• Is Part Of: Cancer & metabolism. Volume 5:Issue 1(2017)
• Page Start: 1
• Page End: 14
• Publication Date: 2017-12
• Subjects: Obesity -- Breast cancer -- Lipid metabolism -- Adipocytes -- Metabolic crosstalk; Cancer -- Endocrine aspects -- Periodicals; Metabolism -- Periodicals; Neoplasms -- metabolism -- Periodicals; Electronic journals; 616.994
• DOI: 10.1186/s40170-016-0163-7
• Languages: English
• ISSNs: 2049-3002

Abstract

Abstract Background Obesity is associated with increased recurrence and reduced survival of breast cancer. Adipocytes constitute a significant component of breast tissue, yet their role in provisioning metabolic substrates to support breast cancer progression is poorly understood. Results Here, we show that co-culture of breast cancer cells with adipocytes revealed cancer cell-stimulated depletion of adipocyte triacylglycerol. Adipocyte-derived free fatty acids were transferred to breast cancer cells, driving fatty acid metabolism via increased CPT1A and electron transport chain complex protein levels, resulting in increased proliferation and migration. Notably, fatty acid transfer to breast cancer cells was enhanced from "obese" adipocytes, concomitant with increased stimulation of cancer cell proliferation and migration. This adipocyte-stimulated breast cancer cell proliferation was dependent on lipolytic processes since HSL/ATGL knockdown attenuated cancer cell responses. Conclusions These findings highlight a novel and potentially important role for adipocyte lipolysis in the provision of metabolic substrates to breast cancer cells, thereby supporting cancer progression.