Panyi Gyorgy, Beeton Christine, Felipe Antonio
Department of Biophysics and Cell Biology, University of Debrecen, , Egyetem ter 1, Life Science Building, Room 2.301, Debrecen, Hungary.
Philos Trans R Soc Lond B Biol Sci. 2014 Feb 3;369(1638):20130106. doi: 10.1098/rstb.2013.0106. Print 2014 Mar 19.
The outcome of a malignant disease depends on the efficacy of the immune system to destroy cancer cells. Key steps in this process, for example the generation of a proper Ca(2+) signal induced by recognition of a specific antigen, are regulated by various ion channel including voltage-gated Kv1.3 and Ca(2+)-activated KCa3.1 K(+) channels, and the interplay between Orai and STIM to produce the Ca(2+)-release-activated Ca(2+) (CRAC) current required for T-cell proliferation and function. Understanding the immune cell subset-specific expression of ion channels along with their particular function in a given cell type, and the role of cancer tissue-dependent factors in the regulation of operation of these ion channels are emerging questions to be addressed in the fight against cancer disease. Answering these questions might lead to a better understanding of the immunosuppression phenomenon in cancer tissue and the development of drugs aimed at skewing the distribution of immune cell types towards killing of the tumour cells.
恶性疾病的预后取决于免疫系统摧毁癌细胞的效力。这一过程中的关键步骤,例如由特定抗原识别诱导产生适当的Ca(2+)信号,受多种离子通道调控,包括电压门控Kv1.3和Ca(2+)激活的KCa3.1 K(+)通道,以及Orai和STIM之间的相互作用以产生T细胞增殖和功能所需的Ca(2+)释放激活Ca(2+)(CRAC)电流。了解离子通道在免疫细胞亚群中的特异性表达及其在特定细胞类型中的特定功能,以及癌症组织依赖性因子在这些离子通道运作调节中的作用,是抗癌斗争中亟待解决的新问题。回答这些问题可能有助于更好地理解癌症组织中的免疫抑制现象,并开发旨在使免疫细胞类型分布偏向杀死肿瘤细胞的药物。