Genito-Urinary Cancer Research Group, School of Cancer, Enabling Sciences and Technology, Paterson Institute for Cancer Research, The University of Manchester, Manchester Academic Health Science Centre, The Christie NHS Foundation Trust, Manchester M20 4BX, UK.
Br J Cancer. 2010 Jan 19;102(2):403-13. doi: 10.1038/sj.bjc.6605481. Epub 2009 Dec 8.
Prostate cancer (CaP) preferentially metastasises to the bone, and we have previously shown that the poly-unsaturated fatty acid (PUFA) arachidonic acid (AA) is a potent stimulator of CaP invasion. Here we present that AA promotes CaP invasion by inducing bone marrow adipocyte formation.
Boyden invasion-chamber assays assessed the ability of dietary oils, their PUFA components, and specific PUFA-loaded adipocytes to induce PC-3 invasion. Lipid transfer and metabolism was followed using deuterated AA and Fourier Transform Infrared spectroscopy (FTIR).
Poly-unsaturated fatty acid constituents, but not their corresponding dietary oils, induced PC-3 invasion. PUFAs induce bone marrow adipocyte (BM-Ad) differentiation with AA inducing higher levels of BM-Ad differentiation, as compared with other PUFAs (3998+/-514.4 vs 932+/-265.8; P=0.00002), which stimulated greater PC-3 invasion than free AA (22 408.5+/-607.4 vs 16 236+/-313.9; P=0.01111) or adipocytes generated in the presence of other PUFAs. In bone marrow co-culture PC-3 and BM-Ad interactions result in direct uptake and metabolism of AA by PC-3 cells, destruction of the adipocyte and subsequent formation of a bone metastasis.
The data supports the hypothesis that AA not only promotes CaP invasion, it also prepares the 'soil', making it more supportive for implantation and propagation of the migrating metastatic cell.
前列腺癌(CaP)优先转移到骨骼,我们之前已经表明,多不饱和脂肪酸(PUFA)花生四烯酸(AA)是促进 CaP 侵袭的有效刺激物。在这里,我们提出 AA 通过诱导骨髓脂肪细胞形成来促进 CaP 侵袭。
Boyden 侵袭室测定评估了饮食油、其 PUFA 成分以及特定 PUFA 负载的脂肪细胞诱导 PC-3 侵袭的能力。使用氘化 AA 和傅里叶变换红外光谱(FTIR)跟踪脂质转移和代谢。
多不饱和脂肪酸成分,但不是它们相应的饮食油,诱导 PC-3 侵袭。PUFAs 诱导骨髓脂肪细胞(BM-Ad)分化,与其他 PUFAs 相比,AA 诱导更高水平的 BM-Ad 分化(3998+/-514.4 与 932+/-265.8;P=0.00002),与游离 AA 相比,BM-Ad 分化刺激更大的 PC-3 侵袭(22408.5+/-607.4 与 16236+/-313.9;P=0.01111)或在其他 PUFAs 存在下生成的脂肪细胞。在骨髓共培养物中,PC-3 和 BM-Ad 相互作用导致 AA 被 PC-3 细胞直接摄取和代谢,脂肪细胞被破坏,随后形成骨转移。
数据支持这样的假设,即 AA 不仅促进 CaP 侵袭,而且还为植入和传播迁移的转移性细胞准备了“土壤”。