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TNFα 和 IFNγ 的抗癌治疗:全面综述。

Anti-cancer therapy with TNFα and IFNγ: A comprehensive review.

机构信息

Laboratory of Molecular Pharmacology, Department of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou, Sichuan, China.

Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong.

出版信息

Cell Prolif. 2018 Aug;51(4):e12441. doi: 10.1111/cpr.12441. Epub 2018 Feb 26.

DOI:10.1111/cpr.12441
PMID:29484738
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6528874/
Abstract

Tumour necrosis factor alpha (TNFα) and interferon gamma (IFNγ) were originally found to be produced by inflammatory cells and play important roles in the immune system and surveillance of tumour growth. By activating distinct signalling pathways of nuclear factor-κB (NF-κB), mitogen-activated protein kinase (MAPK), and JAK/STAT, TNFα and IFNγ were reported to effectively trigger cell death and perform powerful anti-cancer effects. In this review, we will discuss the new advancements of TNFα and IFNγ in anti-cancer therapy.

摘要

肿瘤坏死因子-α(TNFα)和干扰素-γ(IFNγ)最初被发现由炎症细胞产生,在免疫系统和肿瘤生长监测中发挥重要作用。TNFα 和 IFNγ 通过激活核因子-κB(NF-κB)、丝裂原活化蛋白激酶(MAPK)和 JAK/STAT 的不同信号通路,被报道能有效地触发细胞死亡并发挥强大的抗癌作用。在这篇综述中,我们将讨论 TNFα 和 IFNγ 在癌症治疗中的新进展。

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本文引用的文献

1
Vascular-targeted TNFα and IFNγ inhibits orthotopic colorectal tumor growth.血管靶向性肿瘤坏死因子α和干扰素γ可抑制原位结直肠癌的生长。
J Transl Med. 2016 Jun 24;14(1):187. doi: 10.1186/s12967-016-0944-3.
2
Self-targeting of TNF-releasing cancer cells in preclinical models of primary and metastatic tumors.原发性和转移性肿瘤临床前模型中释放肿瘤坏死因子的癌细胞的自我靶向。
Proc Natl Acad Sci U S A. 2016 Feb 23;113(8):2223-8. doi: 10.1073/pnas.1525697113. Epub 2016 Feb 8.
3
Vascular-targeted TNFα improves tumor blood vessel function and enhances antitumor immunity and chemotherapy in colorectal cancer.血管靶向 TNFα 可改善肿瘤血管功能,增强结直肠癌的抗肿瘤免疫和化疗效果。
J Control Release. 2015 Jul 28;210:134-46. doi: 10.1016/j.jconrel.2015.05.282. Epub 2015 May 21.
4
Inhibition of tumor angiogenesis by interferon-γ by suppression of tumor-associated macrophage differentiation.干扰素-γ通过抑制肿瘤相关巨噬细胞分化抑制肿瘤血管生成。
Oncol Res. 2014;21(5):227-35. doi: 10.3727/096504014X13890370410285.
5
The dose-dependent tumor targeting of antibody-IFNγ fusion proteins reveals an unexpected receptor-trapping mechanism in vivo.抗体-IFNγ 融合蛋白的剂量依赖性肿瘤靶向揭示了体内一种意想不到的受体捕获机制。
Cancer Immunol Res. 2014 Jun;2(6):559-67. doi: 10.1158/2326-6066.CIR-13-0182. Epub 2014 Mar 24.
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Targeted Cancer Therapy with Tumor Necrosis Factor-Alpha.肿瘤坏死因子-α的靶向癌症治疗
Biochem Insights. 2008 Jul 22;2008:15-21.
7
Interferon-γ-induced necrosis: an antitumor biotherapeutic perspective.干扰素-γ 诱导坏死:一种抗肿瘤生物治疗的观点。
J Interferon Cytokine Res. 2013 Apr;33(4):171-80. doi: 10.1089/jir.2012.0087.
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T-helper-1-cell cytokines drive cancer into senescence.辅助性 T 细胞 1 型细胞因子促使肿瘤进入衰老状态。
Nature. 2013 Feb 21;494(7437):361-5. doi: 10.1038/nature11824. Epub 2013 Feb 3.
9
Selective targeting of interferon γ to stromal fibroblasts and pericytes as a novel therapeutic approach to inhibit angiogenesis and tumor growth.选择性靶向干扰素 γ 于基质成纤维细胞和周细胞,作为一种新的抑制血管生成和肿瘤生长的治疗方法。
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