Suppr超能文献

咪喹莫特使肿瘤血管正常化:为TLR7激动剂提出新的抗癌治疗适应症

Normalization of tumor vasculature by imiquimod: proposal for a new anticancer therapeutic indication for a TLR7 agonist.

作者信息

Magdalena Jarosz-Biej, Justyna Czapla, Joanna Ciepła, Ryszard Smolarczyk, Alina Drzyzga, Dorota Sprus-Lipka, Ewelina Pilny, Sybilla Matuszczak, Tomasz Cichoń

机构信息

Center for Translational Research and Molecular Biology of Cancer, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Poland.

出版信息

Cancer Immunol Immunother. 2025 Feb 1;74(3):90. doi: 10.1007/s00262-025-03943-2.

Abstract

Imiquimod (IMQ), a drug from aminoquinoline group, is the toll-like receptor 7 (TLR7) agonist. It acts as an immunostimulant and radio-sensitizing agent. IMQ stimulates both innate and adaptive immune response. Despite studies conducted, there are no unambiguous data showing how IMQ affects the condition of tumor blood vessels. Tumor vasculature plays the main role in tumor progression. Formation of abnormal blood vessels increases area of hypoxia which recruits suppressor cells, blocks tumor infiltration by CD8 T lymphocytes, inhibits efficacy of chemoterapeutic drug and leads to cancer relapse. Normalization is a type of therapy targeted at abnormal tumor blood vessels. Here, we demonstrated that 50 µg of IMQ inhibits the growth of melanoma tumors more efficiently, compared to other tested doses and the control group. Dose escalation did not improve the therapeutic antitumor potential of TLR7 agonist. A dose of 50 µg of IMQ most effectively reduced tumor blood vessel density. Imiquimod normalized tumor vasculature both structurally (by reducing vessel tortuosity and increasing pericyte coverage) and functionally (by improving tumor perfusion) in a dose-dependent manner. Hypoxia regions in tumors of treated mice were significantly reduced after IMQ administration. A dose of 50 µg of IMQ had also the greatest impact on the changes in tumor-infiltrating T lymphocytes levels. TLR7 agonist inhibited angiogenesis in treated mice. Functional vascular normalization by IMQ increases the effectiveness of low dose of doxorubicin. Higher dose of IMQ showed worse effects than lower doses including decreased tumor perfusion, increased tumor hypoxia and immunosuppression. This knowledge may help to optimize the combination of the selected IMQ dose with e.g. chemotherapy or radiotherapy to elicit synergistic effect in cancer treatment. To conclude, we outline IMQ repurposing as a vascular normalizing agent. Our research results may contribute to expanding the therapeutic indications for the use of IMQ in anticancer therapy in the future.

摘要

咪喹莫特(IMQ)是一种氨基喹啉类药物,为Toll样受体7(TLR7)激动剂。它可作为免疫刺激剂和放射增敏剂。IMQ能刺激先天性和适应性免疫反应。尽管已开展了多项研究,但尚无明确数据表明IMQ如何影响肿瘤血管状况。肿瘤血管系统在肿瘤进展中起主要作用。异常血管的形成会增加缺氧区域,从而募集抑制细胞,阻碍CD8 T淋巴细胞对肿瘤的浸润,抑制化疗药物的疗效并导致癌症复发。血管正常化是一种针对异常肿瘤血管的治疗方法。在此,我们证明,与其他测试剂量及对照组相比,50μg的IMQ能更有效地抑制黑色素瘤肿瘤生长。剂量递增并未提高TLR7激动剂的治疗抗肿瘤潜力。50μg的IMQ剂量最有效地降低了肿瘤血管密度。咪喹莫特以剂量依赖的方式在结构上(通过降低血管迂曲度和增加周细胞覆盖率)和功能上(通过改善肿瘤灌注)使肿瘤血管正常化。给予IMQ后,经治疗小鼠肿瘤中的缺氧区域显著减少。50μg的IMQ剂量对肿瘤浸润性T淋巴细胞水平的变化也有最大影响。TLR7激动剂抑制了经治疗小鼠的血管生成。IMQ介导的功能性血管正常化提高了低剂量阿霉素的疗效。高剂量IMQ的效果比低剂量更差,包括肿瘤灌注减少、肿瘤缺氧增加和免疫抑制。这一知识可能有助于优化所选IMQ剂量与化疗或放疗等的联合使用,以在癌症治疗中产生协同效应。总之,我们概述了将IMQ重新用作血管正常化剂。我们的研究结果可能有助于在未来扩大IMQ在抗癌治疗中的治疗适应症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/849c/11787066/88c4004f3640/262_2025_3943_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验