Noman Muhammad Zaeem, Messai Yosra, Muret Jane, Hasmim Meriem, Chouaib Salem
INSERM U753, Gustave Roussy Cancer campus, 114 rue Edouard Vaillant, 94805, Villejuif, France.
Cancer Microenviron. 2014 Dec;7(3):153-60. doi: 10.1007/s12307-014-0157-3. Epub 2014 Oct 22.
Accumulating evidence indicate that the behavior of tumorigenic cells is highly influenced by their microenvironment. In this regard, microenvironmental hypoxia plays a determinant role in the emergence of CTC (circulating tumor cells) and CSC (cancer stem cells). CTCs are believed to be indicators of residual disease and thus pose an increased risk of metastasis. In spite of being rare and exposed to immune attack, these cells are capable to escape the immune system of the host. Although CTC play a pivotal role in the metastatic cascade and their prognostic impact has been repeatedly demonstrated, little is known about their escape mechanisms to immune system of the host. Therefore a better knowledge of the immunogenicity of these cells and their cross talk with immune killer cells as well as with tumor microenvironment may represent an exciting new immunotherapy opportunity. In this chapter, we will discuss how hypoxia is involved in the regulation of tumor progression and induction of EMT and cancer stem cell like features. We will also illustrate the relationship between hypoxia and CTC and review how CTC interact with the cells of immune system (both innate and adaptive) in terms of their survival and EMT phenotype. We will attempt to outline how hypoxic stress may confer resistance to CTC by giving them EMT and CSC like phenotype. Finally we will discuss whether the inhibition of hypoxic signaling pathways in different compartments of the solid tumor microenvironment will have an impact on CTC number, resistant phenotype and CTC lysis by immune effectors.
越来越多的证据表明,致瘤细胞的行为受到其微环境的高度影响。在这方面,微环境缺氧在循环肿瘤细胞(CTC)和癌症干细胞(CSC)的出现中起决定性作用。CTC被认为是残留疾病的指标,因此会增加转移风险。尽管这些细胞稀少且易受免疫攻击,但它们能够逃避免疫系统的攻击。尽管CTC在转移级联中起关键作用,并且其预后影响已得到反复证实,但对于它们逃避免疫系统的机制却知之甚少。因此,更好地了解这些细胞的免疫原性以及它们与免疫杀伤细胞以及肿瘤微环境的相互作用,可能代表了一个令人兴奋的新免疫治疗机会。在本章中,我们将讨论缺氧如何参与肿瘤进展的调节以及上皮-间质转化(EMT)和癌症干细胞样特征的诱导。我们还将说明缺氧与CTC之间的关系,并回顾CTC在生存和EMT表型方面如何与免疫系统(先天和适应性)细胞相互作用。我们将试图概述缺氧应激如何通过赋予它们EMT和CSC样表型而使CTC产生抗性。最后,我们将讨论在实体瘤微环境的不同区域抑制缺氧信号通路是否会对CTC数量、抗性表型以及免疫效应器对CTC的裂解产生影响。