Yadav Nalini V S, Barcikowski Arthur, Uehana Yuko, Jacobs Aaron T, Connelly Linda
Department of Pharmaceutical Sciences, Daniel K. Inouye College of Pharmacy, University of Hawaii at Hilo, Hilo, HI, United States.
School of Medicine, California University of Science and Medicine, San Bernardino, CA, United States.
Front Oncol. 2020 Apr 7;10:454. doi: 10.3389/fonc.2020.00454. eCollection 2020.
Obese individuals with breast cancer have a poorer prognosis and higher risk of metastatic disease vs. non-obese patients. Adipose tissue in obese individuals is characterized by an enhanced macrophage infiltration, creating a microenvironment that favors tumor progression. Here, we demonstrate a role for adipocyte-macrophage interactions in the regulation of angiogenesis. Co-culture of THP-1 macrophages with human breast adipocytes led to increased expression of the pro-angiogenic growth factor, vascular endothelial growth factor A (VEGFA). Several adipocyte-derived proteins including leptin, insulin, IL-6, and TNF-α were each capable of increasing VEGFA expression in THP-1 macrophages, identifying these as possible mediators of the changes that were observed with co-culture. Furthermore, analysis of THP-1 culture media by antibody array revealed that THP-1 secrete several other pro-angiogenic signals in response to adipocyte co-culture, including interleukin 8 (IL-8), matrix metalloproteinase 9 (MMP9), pentraxin 3 (PTX3), and serpin E1 (plasminogen activator inhibitor 1, PAI1) after co-culture with human adipocytes. We used an endothelial tube formation assay with human vascular endothelial cells to evaluate the effects of THP-1 culture media on angiogenesis. Here, culture media from THP-1 cells previously exposed to human adipocytes stimulated endothelial tube formation more significantly than THP-1 cells cultured alone. In summary, we find that adipocyte co-culture stimulates the expression of pro-angiogenic mediators in macrophages and has pro-angiogenic effects , thus representing a possible mechanism for the enhanced risk of breast cancer progression in obese individuals.
与非肥胖患者相比,肥胖的乳腺癌患者预后较差,发生转移性疾病的风险更高。肥胖个体的脂肪组织具有巨噬细胞浸润增强的特征,从而形成了有利于肿瘤进展的微环境。在此,我们证明了脂肪细胞与巨噬细胞的相互作用在血管生成调节中的作用。THP-1巨噬细胞与人乳腺脂肪细胞共培养导致促血管生成生长因子血管内皮生长因子A(VEGFA)的表达增加。几种脂肪细胞衍生蛋白,包括瘦素、胰岛素、IL-6和TNF-α,每一种都能够增加THP-1巨噬细胞中VEGFA的表达,表明它们可能是共培养中观察到的变化的介质。此外,通过抗体阵列对THP-1培养基进行分析发现,与人类脂肪细胞共培养后,THP-1会分泌其他几种促血管生成信号,包括白细胞介素8(IL-8)、基质金属蛋白酶9(MMP9)、五聚素3(PTX3)和丝氨酸蛋白酶抑制剂E1(纤溶酶原激活物抑制剂1,PAI1)。我们使用人血管内皮细胞进行内皮管形成试验,以评估THP-1培养基对血管生成的影响。在此,先前暴露于人类脂肪细胞的THP-1细胞的培养基比单独培养的THP-1细胞更显著地刺激内皮管形成。总之,我们发现脂肪细胞共培养可刺激巨噬细胞中促血管生成介质的表达并具有促血管生成作用,因此这可能是肥胖个体乳腺癌进展风险增加的一种机制。