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乳腺肿瘤微环境中炎症细胞因子的串扰

英文原题:Crosstalk of Inflammatory Cytokines within the Breast Tumor Microenvironment.

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Crosstalk of Inflammatory Cytokines within the Breast Tumor Microenvironment.

PubMed 2023/02/16(内容时间) Int J Mol Sci Q1 · IF 5.6(JCR 2025)

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中文摘要

多种免疫细胞和免疫活性细胞,包括树突状细胞、巨噬细胞、脂肪细胞、NK 细胞、T细胞和B细胞,与肿瘤学这一复杂学科显著相关。细胞毒性先天性和适应性免疫细胞可以阻断肿瘤增殖,而其他细胞则可以阻止免疫系统排斥恶性细胞,并为肿瘤进展提供有利环境。这些细胞通过细胞因子——一种化学信使——以内分泌、旁分泌或自分泌方式与微环境进行通讯。这些细胞因子在健康和疾病中发挥重要作用,特别是在宿主对感染和炎症的免疫反应中。它们包括趋化因子、白细胞介素(ILs)、脂肪因子、干扰素、集落刺激因子(CSFs)和肿瘤坏死因子(TNF),这些因子由多种细胞产生,包括免疫细胞如巨噬细胞、B细胞、T细胞和肥大细胞,以及内皮细胞、成纤维细胞、多种基质细胞和一些癌细胞。细胞因子在癌症和癌症相关炎症中发挥关键作用,对肿瘤拮抗或肿瘤促进功能具有直接和间接影响。它们作为免疫刺激介质已被广泛研究,可促进免疫细胞的生成、迁移和募集,从而有助于有效的抗肿瘤免疫反应或促肿瘤微环境。

因此,在许多癌症如乳腺癌中,包括瘦素、IL-1B、IL-6、IL-8、IL-23、IL-17和IL-10在内的细胞因子刺激癌症增殖和/或侵袭,而其他包括IL-2、IL-12和IFN-γ在内的细胞因子则抑制癌症增殖和/或侵袭并增强机体的抗肿瘤防御。事实上,细胞因子在肿瘤发生中的多功能作用将促进我们对肿瘤微环境中细胞因子串扰途径的理解,例如 JAK/STAT、PI3K、AKT、Rac、MAPK、NF-κB、JunB、cFos 和 mTOR,这些途径参与血管生成、癌症增殖和转移。

因此,靶向和阻断促肿瘤细胞因子或激活和扩增抑肿瘤细胞因子被认为是针对癌症的治疗方法。在此,我们重点关注炎症细胞因子系统在促肿瘤和抗肿瘤免疫反应中的作用,讨论参与癌症免疫反应的细胞因子途径以及一些抗癌治疗应用。

展开英文摘要原文

Several immune and immunocompetent cells, including dendritic cells, macrophages, adipocytes, natural killer cells, T cells, and B cells, are significantly correlated with the complex discipline of oncology. Cytotoxic innate and adaptive immune cells can block tumor proliferation, and others can prevent the immune system from rejecting malignant cells and provide a favorable environment for tumor progression. These cells communicate with the microenvironment through cytokines, a chemical messenger, in an endocrine, paracrine, or autocrine manner. These cytokines play an important role in health and disease, particularly in host immune responses to infection and inflammation.

They include chemokines, interleukins (ILs), adipokines, interferons, colony-stimulating factors (CSFs), and tumor necrosis factor (TNF), which are produced by a wide range of cells, including immune cells, such as macrophages, B-cells, T-cells, and mast cells, as well as endothelial cells, fibroblasts, a variety of stromal cells, and some cancer cells.

Cytokines play a crucial role in cancer and cancer-related inflammation, with direct and indirect effects on tumor antagonistic or tumor promoting functions. They have been extensively researched as immunostimulatory mediators to promote the generation, migration and recruitment of immune cells that contribute to an effective antitumor immune response or pro-tumor microenvironment.

Thus, in many cancers such as breast cancer, cytokines including leptin, IL-1B, IL-6, IL-8, IL-23, IL-17, and IL-10 stimulate while others including IL-2, IL-12, and IFN-γ, inhibit cancer proliferation and/or invasion and enhance the body's anti-tumor defense.

Indeed, the multifactorial functions of cytokines in tumorigenesis will advance our understanding of cytokine crosstalk pathways in the tumor microenvironment, such as JAK/STAT, PI3K, AKT, Rac, MAPK, NF-κB, JunB, cFos, and mTOR, which are involved in angiogenesis, cancer proliferation and metastasis. Accordingly, targeting and blocking tumor-promoting cytokines or activating and amplifying tumor-inhibiting cytokines are considered cancer-directed therapies.

Here, we focus on the role of the inflammatory cytokine system in pro- and anti-tumor immune responses, discuss cytokine pathways involved in immune responses to cancer and some anti-cancer therapeutic applications.

论文信息

作者
Habanjar O、Bingula R、Decombat C、Diab-Assaf M、Caldefie-Chezet F、Delort L
单位
Université Clermont-Auvergne, INRAE, UNH, Unité de Nutrition Humaine, CRNH-Auvergne, 63000 Clermont-Ferrand, France.France
文献类型
综述
期刊
International journal of molecular sciences2023 Feb 16
原文标识
PubMed 36835413 · DOI 10.3390/ijms24044002