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实体瘤中癌症干细胞的免疫学。一篇综述。

Immunology of cancer stem cells in solid tumours. A review.

机构信息

Unit of Immuno-Biotherapy of Melanoma and Solid Tumors, Division of Molecular Oncology, San Raffaele Scientific Institute, Milan, Italy.

Unit of Immuno-Biotherapy of Melanoma and Solid Tumors, Division of Molecular Oncology, San Raffaele Scientific Institute, Milan, Italy.

出版信息

Eur J Cancer. 2014 Feb;50(3):649-55. doi: 10.1016/j.ejca.2013.11.014. Epub 2013 Dec 12.

Abstract

Cancer stem cells (CSCs) represent a minor subpopulation of tumour cells that share some features with the normal stem cells of the tissue from which tumour derives and have the properties of self-renewal, multiple differentiation and tumour initiation (tumour-initiating cells, TICs). Thus CSCs/TICs need to survive cancer therapies in order to provide new, more differentiated, metastatic-prone tumour cells. This occurs through different signals delivered within the tumour microenvironment. The immune system of cancer patients may recognise CSCs/TICs and kill them though it is unclear whether this may occur in vivo during spontaneous tumour growth. This review summarises findings on the immunological profile of CSCs/TICs as compared with neoplastic non-stem cells and discusses the possible antigens recognised by the patients' immune system, the in vitro and the potential in vivo immunogenicity of such antigens and the ability of human CSCs/TICs to down-regulate the immune response by the release of a variety of suppressive factors. We conclude that available data on immunological characterisation of CSCs/TICs may be useful in the perspective of designing new translational immunotherapy protocols targeting CSCs/TICs.

摘要

癌症干细胞(CSCs)代表肿瘤细胞中的一个小亚群,它们具有与肿瘤来源组织的正常干细胞相似的特征,并具有自我更新、多向分化和肿瘤起始(肿瘤起始细胞,TICs)的特性。因此,CSCs/TICs 需要在癌症治疗中存活下来,以提供新的、更分化的、易转移的肿瘤细胞。这是通过肿瘤微环境中的不同信号传递来实现的。癌症患者的免疫系统可能会识别 CSCs/TICs 并杀死它们,但目前尚不清楚在自发肿瘤生长过程中是否会在体内发生这种情况。这篇综述总结了 CSCs/TICs 与肿瘤非干细胞的免疫表型特征的研究结果,并讨论了患者免疫系统识别的可能抗原、这些抗原的体外和潜在体内免疫原性以及人类 CSCs/TICs 通过释放多种抑制因子来下调免疫反应的能力。我们得出结论,关于 CSCs/TICs 的免疫特征的现有数据可能有助于设计针对 CSCs/TICs 的新转化免疫治疗方案。

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