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靶向黑色素瘤肿瘤微环境中的抗癌免疫:释放佐剂、药物和植物化学物的潜力

英文原题:Targeting anticancer immunity in melanoma tumour microenvironment: unleashing the potential of adjuvants, drugs, and phytochemicals.

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Targeting anticancer immunity in melanoma tumour microenvironment: unleashing the potential of adjuvants, drugs, and phytochemicals.

PubMed 2024/08/07(内容时间) J Drug Target Q1 · IF 4.7(JCR 2025)

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中文摘要

黑色素瘤因其侵袭性和有限的治疗方式而在肿瘤学中构成挑战。黑色素瘤的肿瘤微环境(TME)具有独特性质,如免疫抑制和高密度环境、异常的血管系统以及大量基质细胞和免疫抑制细胞。近年来,大量实验集中于增强免疫系统以有效清除恶性细胞。由植物化学物质、toll样受体(TLR)激动剂和细胞因子组成的佐剂在触发抗肿瘤免疫和增强抗癌治疗疗效方面显示出令人鼓舞的结果。这些佐剂可以刺激树突状细胞(DCs)的成熟和细胞毒性CD8+ T淋巴细胞(CTLs)的浸润。

此外,纳米载体可以帮助将免疫调节剂和抗原直接递送至肿瘤基质,从而提高其对抗恶性细胞的效力。利用植物化学物质、激动剂和其他佐剂重塑黑色素瘤TME可以与当前的治疗方式相结合以改善治疗结果。这篇综述文章探讨了佐剂、药物及其纳米制剂在增强巨噬细胞、CTLs和自然杀伤(NK)细胞抗癌效力方面的潜力。

此外,还将讨论这些药物抑制黑色素瘤TME免疫抑制成分(如巨噬细胞、基质细胞和髓系细胞的免疫抑制亚群)功能的能力。

展开英文摘要原文

Melanoma poses a challenge in oncology because of its aggressive nature and limited treatment modalities. The tumour microenvironment (TME) in melanoma contains unique properties such as an immunosuppressive and high-density environment, unusual vasculature, and a high number of stromal and immunosuppressive cells. In recent years, numerous experiments have focused on boosting the immune system to effectively remove malignant cells.

Adjuvants, consisting of phytochemicals, toll-like receptor (TLR) agonists, and cytokines, have shown encouraging results in triggering antitumor immunity and augmenting the therapeutic effectiveness of anticancer therapy. These adjuvants can stimulate the maturation of dendritic cells (DCs) and infiltration of cytotoxic CD8+ T lymphocytes (CTLs).

Furthermore, nanocarriers can help to deliver immunomodulators and antigens directly to the tumour stroma, thereby improving their efficacy against malignant cells. The remodelling of melanoma TME utilising phytochemicals, agonists, and other adjuvants can be combined with current modalities for improving therapy outcomes. This review article explores the potential of adjuvants, drugs, and their nanoformulations in enhancing the anticancer potency of macrophages, CTLs, and natural killer (NK) cells.

Additionally, the capacity of these agents to repress the function of immunosuppressive components of melanoma TME, such as immunosuppressive subsets of macrophages, stromal and myeloid cells will be discussed.

论文信息

作者
Wang J、Wang Y、Jiang X
第一作者单位
Emergency Department, Zhejiang Provincial General Hospital of the Chinese People's Armed Police Force, Zhejiang, China.China
通讯作者单位
Respiratory and Oncology Department, Zhejiang Provincial General Hospital of the Chinese People's Armed Police Force, Zhejiang, China.China
文献类型
综述
期刊
Journal of drug targeting2024 Nov
原文标识
PubMed 39041142 · DOI 10.1080/1061186X.2024.2384071