The Role of Diet Related Short-Chain Fatty Acids in Colorectal Cancer Metabolism and Survival: Prevention and Therapeutic Implications

丁酸盐 结直肠癌 糖酵解 抗性淀粉 丙酸盐 癌症 癌症研究 细胞生物学 生物 新陈代谢 生物化学 化学 发酵 遗传学 淀粉
作者
Sara Gomes,Cláudia S. Oliveira,João Azevedo‐Silva,Marta R. Casanova,Judite Barreto,Helena Pereira,Susana R. Chaves,L. R. Rodrigues,Margarida Casal,Manuela Côrte‐Real,Fátima Baltazar,Ana Preto
出处
期刊:Current Medicinal Chemistry [Bentham Science]
卷期号:27 (24): 4087-4108 被引量:87
标识
DOI:10.2174/0929867325666180530102050
摘要

: Colorectal Cancer (CRC) is a major cause of cancer-related death worldwide. CRC increased risk has been associated with alterations in the intestinal microbiota, with decreased production of Short Chain Fatty Acids (SCFAs). SCFAs produced in the human colon are the major products of bacterial fermentation of undigested dietary fiber and starch. While colonocytes use the three major SCFAs, namely acetate, propionate and butyrate, as energy sources, transformed CRC cells primarily undergo aerobic glycolysis. Compared to normal colonocytes, CRC cells exhibit increased sensitivity to SCFAs, thus indicating they play an important role in cell homeostasis. Manipulation of SCFA levels in the intestine, through changes in microbiota, has therefore emerged as a potential preventive/therapeutic strategy for CRC. Interest in understanding SCFAs mechanism of action in CRC cells has increased in the last years. Several SCFA transporters like SMCT-1, MCT-1 and aquaporins have been identified as the main transmembrane transporters in intestinal cells. Recently, it was shown that acetate promotes plasma membrane re-localization of MCT-1 and triggers changes in the glucose metabolism. SCFAs induce apoptotic cell death in CRC cells, and further mechanisms have been discovered, including the involvement of lysosomal membrane permeabilization, associated with mitochondria dysfunction and degradation. : In this review, we will discuss the current knowledge on the transport of SCFAs by CRC cells and their effects on CRC metabolism and survival. The impact of increasing SCFA production by manipulation of colon microbiota on the prevention/therapy of CRC will also be addressed.
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