Menendez Javier A, Lupu Ruth
Foundation of the Recerca Bio-Medical Institute of Girona Dr Josep Trueta, University Hospital of Girona, Dr Josep Trueta, Girona, Catalonia, Spain.
Curr Opin Clin Nutr Metab Care. 2006 Jul;9(4):346-57. doi: 10.1097/01.mco.0000232893.21050.15.
This review documents our rapidly changing perspectives on the function of fatty acid synthase-catalyzed endogenous fatty acid biogenesis in cancer biology.
Up-regulation of fatty acid synthase gene expression and fatty acid synthase biosynthetic activity are molecular events accompanying the pathogenesis and natural history of cancer disease. First, the increased fatty acid synthase gene expression in precursor, preinvasive and invasive cancer lesions appears to represent an indirect, early epiphenomenon, occurring in response to a microenvironment containing regions of poor oxygenation and high acidity due to, for example, lack of an adequate angiogenesis and/or nutritional supply. Second, aberrant transduction cascades driven by cancer-associated oncogenic changes subvert the downregulatory effects of circulating fatty acids. Third, fatty acid synthase-dependent endogenous fatty acid metabolism actively contributes to cancer evolution by specifically regulating the expression, activity and/or cellular localization of proteins closely related to malignant transformation and/or cancer progression.
Fatty acid synthase-catalyzed endogenous fatty acid metabolism appears to be an obligatory acquisition selecting a biologically aggressive sub-group of cancer cells capable of growth and survival upon stresses such as hypoxia, low pH and/or nutritional deprivation. Considering that an ever-growing body of evidence demonstrates that fatty acid synthase-driven signalling actively regulates key cancer-controlling networks, we may hereafter redefine fatty acid synthase as a metabolic oncogene in human cancer cells.
本综述阐述了我们对脂肪酸合酶催化的内源性脂肪酸生物合成在癌症生物学中功能的快速变化的观点。
脂肪酸合酶基因表达上调和脂肪酸合酶生物合成活性是伴随癌症疾病发病机制和自然史的分子事件。首先,在前体、癌前和浸润性癌病变中脂肪酸合酶基因表达增加似乎代表一种间接的早期现象,是对例如由于缺乏充足的血管生成和/或营养供应而导致的含低氧和高酸度区域的微环境的反应。其次,由癌症相关致癌变化驱动的异常转导级联破坏了循环脂肪酸的下调作用。第三,脂肪酸合酶依赖性内源性脂肪酸代谢通过特异性调节与恶性转化和/或癌症进展密切相关的蛋白质的表达、活性和/或细胞定位,积极促进癌症进展。
脂肪酸合酶催化的内源性脂肪酸代谢似乎是一种必然获得,选择了一组具有生物学侵袭性的癌细胞亚群,这些癌细胞能够在诸如缺氧、低pH值和/或营养剥夺等应激条件下生长和存活。鉴于越来越多的证据表明脂肪酸合酶驱动的信号传导积极调节关键的癌症控制网络,我们此后可能会将脂肪酸合酶重新定义为人类癌细胞中的代谢癌基因。