Cantini Giulia, Di Franco Alessandra, Mannelli Massimo, Scimè Anthony, Maggi Mario, Luconi Michaela
Endocrinology Unit, Department of Experimental and Clinical Biomedical Sciences "Mario Serio," University of Florence, Florence, Italy.
Molecular, Cellular and Integrative Physiology, Faculty of Health, York University, Toronto, ON, Canada.
Front Cell Dev Biol. 2020 May 15;8:332. doi: 10.3389/fcell.2020.00332. eCollection 2020.
Adipose tissue in physiological and in metabolically altered conditions (obesity, diabetes, metabolic syndrome) strictly interacts with the developing tumors both systemically and locally. In addition to the cancer-associated fibroblasts, adipose cells have also recently been described among the pivotal actors of the tumor microenvironment responsible for sustaining tumor development and progression. In particular, emerging evidence suggests that not only the mature adipocytes but also the adipose stem cells (ASCs) are able to establish a strict crosstalk with the tumour cells, thus resulting in a reciprocal reprogramming of both the tumor and adipose components. This review will focus on the metabolic changes induced by this interaction as a driver of fate determination occurring in cancer-associated ASCs (CA-ASCs) to support the tumor metabolic requirements. We will showcase the major role played by the metabolic changes occurring in the adipose tumor microenvironment that regulates ASC fate and consequently cancer progression. Our new results will also highlight the CA-ASC response by using a coculture system of primary ASCs grown with cancer cells originating from two different types of adrenal cancers [adrenocortical carcinoma (ACC) and pheochromocytoma]. In conclusion, the different factors involved in this crosstalk process will be analyzed and their effects on the adipocyte differentiation potential and functions of CA-ASCs will be discussed.
在生理状态以及代谢改变的情况下(肥胖、糖尿病、代谢综合征),脂肪组织与正在发展的肿瘤在全身和局部层面都存在着紧密的相互作用。除了癌症相关成纤维细胞外,脂肪细胞最近也被认为是肿瘤微环境中维持肿瘤发展和进展的关键因素之一。特别是,新出现的证据表明,不仅成熟脂肪细胞,而且脂肪干细胞(ASC)都能够与肿瘤细胞建立紧密的相互作用,从而导致肿瘤和脂肪成分的相互重编程。本综述将聚焦于这种相互作用所引发的代谢变化,这些变化作为癌症相关脂肪干细胞(CA-ASC)命运决定的驱动因素,以支持肿瘤的代谢需求。我们将展示脂肪肿瘤微环境中发生的代谢变化在调节ASC命运从而影响癌症进展方面所起的主要作用。我们的新结果还将通过使用原代ASC与源自两种不同类型肾上腺癌[肾上腺皮质癌(ACC)和嗜铬细胞瘤]的癌细胞共培养系统来突出CA-ASC的反应。总之,将分析这种相互作用过程中涉及的不同因素,并讨论它们对CA-ASC的脂肪细胞分化潜能和功能的影响。