工程化益生菌用于肿瘤靶向联合化学免疫治疗
Engineered probiotics for tumor-targeted combination chemoimmunotherapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Multifaceted Interplay between Hormones, Growth Factors and Hypoxia in the Tumor Microenvironment.
Multifaceted Interplay between Hormones, Growth Factors and Hypoxia in the Tumor Microenvironment.
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激素和生长因子(GFs)是参与调控多种细胞过程的信号分子。它们在正常细胞和肿瘤细胞中均发挥重要作用,通过与靶细胞上的特异性受体结合并激活下游信号级联来发挥作用。肿瘤进展的各阶段受到激素和GF信号的影響。缺氧作为癌症进展的一个标志,促进肿瘤的可塑性和异质性。由于细胞快速增殖超出血液供应,大多数实体瘤包含一个缺氧核心。在这些情况下,缺氧诱导因子(HIFs)在肿瘤细胞适应其新环境的过程中发挥核心作用,显著重塑其转录谱。HIF信号受多种因素调节,包括激素和GFs,这些因素激活的信号通路增强肿瘤生长和转移潜能,并损害对治疗的反应。在这篇综述中,我们总结了激素和GFs在癌症发生和进展中的作用,特别关注缺氧以及与HIF蛋白的相互作用。我们还讨论了缺氧如何影响癌症免疫治疗的疗效,考虑到缺氧环境可能作为免疫排斥表型的决定因素,并且是过继细胞治疗成功的主要障碍。
Hormones and growth factors (GFs) are signaling molecules implicated in the regulation of a variety of cellular processes. They play important roles in both healthy and tumor cells, where they function by binding to specific receptors on target cells and activating downstream signaling cascades. The stages of tumor progression are influenced by hormones and GF signaling. Hypoxia, a hallmark of cancer progression, contributes to tumor plasticity and heterogeneity. Most solid tumors contain a hypoxic core due to rapid cellular proliferation that outgrows the blood supply.
In these circumstances, hypoxia-inducible factors (HIFs) play a central role in the adaptation of tumor cells to their new environment, dramatically reshaping their transcriptional profile. HIF signaling is modulated by a variety of factors including hormones and GFs, which activate signaling pathways that enhance tumor growth and metastatic potential and impair responses to therapy. In this review, we summarize the role of hormones and GFs during cancer onset and progression with a particular focus on hypoxia and the interplay with HIF proteins.
We also discuss how hypoxia influences the efficacy of cancer immunotherapy, considering that a hypoxic environment may act as a determinant of the immune-excluded phenotype and a major hindrance to the success of adoptive cell therapies.
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