School of Molecular and Cell Biology, University of the Witwatersrand, Johannesburg, South Africa.
FEBS J. 2019 Nov;286(21):4192-4208. doi: 10.1111/febs.15018. Epub 2019 Aug 12.
Cholesterol dyshomeostasis in cancer cells leads to intracellular cholesterol accumulation, which imparts drug resistance and allows these cells to evade apoptotic signalling processes and maintain continuous cell division and proliferation. Therefore, cholesterol lowering in cancer cells has been envisaged as a potential anticancer strategy. In this direction, two therapeutic strategies have been proposed: (a) to inhibit the biosynthesis of cholesterol in the cells and (b) to deplete excess cholesterol from cancer cells. In the first phase of this review, we collate the cancer signalling pathways (particularly in breast cancer) that are perturbed by cholesterol dyshomeostasis and highlight recent drug discovery efforts to develop cholesterol-lowering compounds, some of which are currently under clinical trials. In the second phase, based on the analysis of the available scientific evidence, we conceptualize and argue that the depletion of excess cholesterol could sensitize cancer cells to available therapeutics and may also help to alleviate cancer drug resistance.
癌细胞中的胆固醇动态平衡失调导致细胞内胆固醇积累,从而赋予这些细胞耐药性,并使其能够逃避凋亡信号转导过程,保持持续的细胞分裂和增殖。因此,降低癌细胞中的胆固醇已被视为一种潜在的抗癌策略。为此,提出了两种治疗策略:(a)抑制细胞内胆固醇的生物合成,(b)从癌细胞中去除多余的胆固醇。在本综述的第一阶段,我们整理了受胆固醇动态平衡失调干扰的癌症信号通路(特别是在乳腺癌中),并强调了最近为开发降低胆固醇的化合物而进行的药物发现工作,其中一些目前正在临床试验中。在第二阶段,根据现有科学证据的分析,我们构想并认为,去除多余的胆固醇可以使癌细胞对现有治疗药物敏感,也可能有助于缓解癌症耐药性。