Fatty acids as potential adjunctive colorectal chemotherapeutic agents

被引:62
作者
Fauser, Jane K. [1 ,2 ]
Prisciandaro, Luca D. [1 ]
Cummins, Adrian G. [2 ]
Howarth, Gordon S. [1 ,3 ]
机构
[1] Univ Adelaide, Sch Anim & Vet Sci, Adelaide, SA, Australia
[2] Queen Elizabeth Hosp, Dept Gastroenterol & Hepatol, Woodville, SA 5011, Australia
[3] Children Youth & Womens Hlth Serv, Dept Gastroenterol, Adelaide, SA, Australia
关键词
fatty acids; colorectal cancer; chain length fatty acids; apoptosis; chemotherapy; COLON-CANCER CELLS; CONJUGATED LINOLEIC-ACID; BUTYRATE-INDUCED DIFFERENTIATION; FOCAL ADHESION KINASE; SODIUM-BUTYRATE; CACO-2; CELLS; MITOCHONDRIAL PATHWAY; MEDIATED APOPTOSIS; GENE-EXPRESSION; SMALL-INTESTINE;
D O I
10.4161/cbt.11.8.15281
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Fatty acids (FA) are bioactive molecules which have potential as adjunctive chemotherapeutic agents. FA are classified as short-, medium; or long-chain on the basis of the number of carbon atoms in the aliphatic chain and have been reported to induce apoptosis in vitro in a range of cancer cell types, including breast, tongue, cervix and colorectal. However, to date the chain length exerting optimal anti-neoplastic properties remains undefined. Short chain fatty acids, such as butyrate (C4:0), have induced high rates of in vitro apoptosis, presumably related to epigenetic modification, cell cycle arrest and activation of pro-apoptotic genes. Medium chain fatty acids have demonstrated in vivo and in vitro cytotoxic and anti-microbial properties; however, scant evidence currently exists on their anti-neoplastic potential. Longer unsaturated fatty acids (C16-24:.3-9), including conjugated linoleic acid and eicosapentaenoic acid, also exhibit in vitro anti-proliferative actions, including induction of oxidative stress and modification of intracellular signaling pathways. Although incorporation of FA into CRC chemotherapy regimens is in its infancy, evidence is accumulating to allow identification of the FA chain length capable of exerting the most effective antineoplastic activity.
引用
收藏
页码:724 / 731
页数:8
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