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Toll 样受体导向的人类癌症治疗干预:分子和免疫学观点。

Toll-like receptor-guided therapeutic intervention of human cancers: molecular and immunological perspectives.

机构信息

Integrative Biochemistry & Immunology Laboratory, Department of Animal Science, Kazi Nazrul University, Asansol, West Bengal, India.

Department of Microbiology, Shahr-e-Qods Branch, Islamic Azad University, Tehran, Iran.

出版信息

Front Immunol. 2023 Sep 26;14:1244345. doi: 10.3389/fimmu.2023.1244345. eCollection 2023.

Abstract

Toll-like receptors (TLRs) serve as the body's first line of defense, recognizing both pathogen-expressed molecules and host-derived molecules released from damaged or dying cells. The wide distribution of different cell types, ranging from epithelial to immune cells, highlights the crucial roles of TLRs in linking innate and adaptive immunity. Upon stimulation, TLRs binding mediates the expression of several adapter proteins and downstream kinases, that lead to the induction of several other signaling molecules such as key pro-inflammatory mediators. Indeed, extraordinary progress in immunobiological research has suggested that TLRs could represent promising targets for the therapeutic intervention of inflammation-associated diseases, autoimmune diseases, microbial infections as well as human cancers. So far, for the prevention and possible treatment of inflammatory diseases, various TLR antagonists/inhibitors have shown to be efficacious at several stages from pre-clinical evaluation to clinical trials. Therefore, the fascinating role of TLRs in modulating the human immune responses at innate as well as adaptive levels directed the scientists to opt for these immune sensor proteins as suitable targets for developing chemotherapeutics and immunotherapeutics against cancer. Hitherto, several TLR-targeting small molecules (e.g., Pam3CSK4, Poly (I:C), Poly (A:U)), chemical compounds, phytocompounds (e.g., Curcumin), peptides, and antibodies have been found to confer protection against several types of cancers. However, administration of inappropriate doses of such TLR-modulating therapeutics or a wrong infusion administration is reported to induce detrimental outcomes. This review summarizes the current findings on the molecular and structural biology of TLRs and gives an overview of the potency and promises of TLR-directed therapeutic strategies against cancers by discussing the findings from established and pipeline discoveries.

摘要

Toll 样受体 (TLRs) 作为机体的第一道防线,可识别病原体表达的分子和受损或死亡细胞释放的宿主来源分子。不同细胞类型(从上皮细胞到免疫细胞)的广泛分布,突出了 TLR 在连接固有免疫和适应性免疫中的关键作用。在受到刺激后,TLR 结合介导几种衔接蛋白和下游激酶的表达,从而诱导几种其他信号分子的表达,如关键的促炎介质。事实上,免疫生物学研究的非凡进展表明,TLRs 可能成为炎症相关疾病、自身免疫性疾病、微生物感染以及人类癌症治疗干预的有前途的靶点。到目前为止,为了预防和可能治疗炎症性疾病,各种 TLR 拮抗剂/抑制剂已在临床前评估到临床试验的多个阶段显示出疗效。因此,TLRs 在调节人类固有和适应性免疫反应方面的迷人作用促使科学家选择这些免疫传感器蛋白作为开发针对癌症的化学疗法和免疫疗法的合适靶点。迄今为止,已经发现几种 TLR 靶向小分子(例如 Pam3CSK4、Poly (I:C)、Poly (A:U))、化学化合物、植物化合物(例如姜黄素)、肽和抗体可预防多种类型的癌症。然而,据报道,不适当剂量的此类 TLR 调节治疗药物或错误的输注给药会导致有害结果。本综述总结了 TLR 的分子和结构生物学的最新发现,并通过讨论已建立和管道发现的结果,概述了 TLR 靶向治疗策略在癌症中的效力和潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef6/10562563/653915c0cd98/fimmu-14-1244345-g001.jpg

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