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前列腺癌中的肿瘤固有免疫微环境:可溶性因子和细胞效应器概述

The tumor innate immune microenvironment in prostate cancer: an overview of soluble factors and cellular effectors.

作者信息

Palano Maria Teresa, Gallazzi Matteo, Cucchiara Martina, Dehò Federico, Capogrosso Paolo, Bruno Antonino, Mortara Lorenzo

机构信息

Laboratory of Innate Immunity, Unit of Molecular Pathology, Biochemistry and Immunology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) MultiMedica, 20138 Milan, Italy.

Laboratory of Immunology and General Pathology, Department of Biotechnology and Life Sciences, University of Insubria, 21100 Varese, Italy.

出版信息

Explor Target Antitumor Ther. 2022;3(5):694-718. doi: 10.37349/etat.2022.00108. Epub 2022 Oct 31.

Abstract

Prostate cancer (PCa) accounts as the most common non-cutaneous disease affecting males, and as the first cancer, for incidence, in male. With the introduction of the concept of immunoscore, PCa has been classified as a cold tumor, thus driving the attention in the development of strategies aimed at blocking the infiltration/activation of immunosuppressive cells, while favoring the infiltration/activation of anti-tumor immune cells. Even if immunotherapy has revolutionized the approaches to cancer therapy, there is still a window failure, due to the immune cell plasticity within PCa, that can acquire pro-tumor features, subsequent to the tumor microenvironment (TME) capability to polarize them. This review discussed selected relevant soluble factors [transforming growth factor-beta (TGFβ), interleukin-6 (IL-6), IL-10, IL-23] and cellular components of the innate immunity, as drivers of tumor progression, immunosuppression, and angiogenesis within the PCa-TME.

摘要

前列腺癌(PCa)是影响男性最常见的非皮肤疾病,也是男性发病率排名第一的癌症。随着免疫评分概念的引入,PCa被归类为冷肿瘤,这促使人们关注旨在阻断免疫抑制细胞浸润/激活,同时促进抗肿瘤免疫细胞浸润/激活的策略的开发。尽管免疫疗法彻底改变了癌症治疗方法,但由于PCa内免疫细胞的可塑性,仍存在一部分治疗失败的情况,在肿瘤微环境(TME)使它们极化后,这些免疫细胞可获得促肿瘤特征。本综述讨论了前列腺癌肿瘤微环境中选定的相关可溶性因子[转化生长因子-β(TGFβ)、白细胞介素-6(IL-6)、IL-10、IL-23]和先天免疫的细胞成分,它们是肿瘤进展、免疫抑制和血管生成的驱动因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98f1/9630328/e087e56b6cd1/etat-03-1002108-g001.jpg

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