Institute of Biochemistry, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
Int J Hyperthermia. 2013 Aug;29(5):491-9. doi: 10.3109/02656736.2013.808765. Epub 2013 Jul 10.
Hyperthermia is a promising treatment modality for cancer in combination both with radio- and chemotherapy. In spite of its great therapeutic potential, the underlying molecular mechanisms still remain to be clarified. Due to lipid imbalances and 'membrane defects' most of the tumour cells possess elevated membrane fluidity. However, further increasing membrane fluidity to sensitise to chemo- or radiotherapy could have some other effects. In fact, hyperfluidisation of cell membrane induced by membrane fluidiser initiates a stress response as the heat shock protein response, which may modulate positively or negatively apoptotic cell death. Overviewing some recent findings based on a technology allowing direct imaging of lipid rafts in live cells and lipidomics, novel aspects of the intimate relationship between the 'membrane stress' of tumour cells and the cellular heat shock response will be highlighted. Our findings lend support to both the importance of membrane remodelling and the release of lipid signals initiating stress protein response, which can operate in tandem to control the extent of the ultimate cellular thermosensitivity. Overall, we suggest that the fluidity variable of membranes should be used as an independent factor for predicting the efficacy of combinational cancer therapies.
热疗是一种有前途的癌症治疗方法,可与放化疗联合使用。尽管具有巨大的治疗潜力,但潜在的分子机制仍有待阐明。由于脂质失衡和“膜缺陷”,大多数肿瘤细胞具有升高的膜流动性。然而,进一步增加膜流动性以使肿瘤对化疗或放疗敏感可能会产生一些其他影响。事实上,由膜流动性调节剂诱导的细胞膜超流动性会引发应激反应,如热休克蛋白反应,这可能会对细胞凋亡产生正向或负向调节作用。基于一种允许直接在活细胞中成像脂筏和脂质组学的技术,综述了肿瘤细胞“膜应激”与细胞热休克反应之间密切关系的一些新方面。我们的发现支持了膜重塑和释放引发应激蛋白反应的脂质信号的重要性,这两者可以协同作用,控制最终细胞热敏感性的程度。总的来说,我们认为膜的流动性变量可以作为预测联合癌症治疗疗效的独立因素。