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CR5/CCL5 轴与不良预后相关,抑制该轴可减少口腔鳞状细胞癌的转移。

CR5/CCL5 axis is linked to a poor outcome, and inhibition reduces metastasis in oral squamous cell carcinoma.

机构信息

Facultad de Odontología, Universidad de los Andes, Santiago, Chile.

Centro de Investigación e Innovación Biomédica, Universidad de los Andes, Santiago, Chile.

出版信息

J Cancer Res Clin Oncol. 2023 Dec;149(19):17335-17346. doi: 10.1007/s00432-023-05443-1. Epub 2023 Oct 13.

Abstract

PURPOSE

The CCR5/CCL5 axis is essential for interactions between malignant cells and microenvironment components, promoting tumor progression in oral squamous cell carcinoma (OSCC). This study aims to evaluate the association of CCL5 and CCR5 with the behavior of oral cancer and assess the therapeutic potential of a CCR5 antagonist.

METHODS

A retrospective study to analyze CCR5 and CCL5 expression on paraffin-embedded tissues was performed. In cell lines, rhCCL5 was added to induce CCR5-related pathways, and Maraviroc and shRNA against CCR5 were used to neutralize the receptor. Finally, an in vivo murine orthotopic xenograft model of tongue cancer was used to evaluate Maraviroc as an oncologic therapy. After 15 days, the mice were killed, and the primary tumors and cervical lymph nodes were analyzed.

RESULTS

The expression of CCR5 was associated with clinical stage and metastasis, and CCL5 was related to overall survival. Adding rhCCL5 induced cell proliferation, while shRNA and Maraviroc reduced it in a dose-dependent manner. Maraviroc treatment also increased apoptosis and modified cytoskeletal organization. In vivo, Maraviroc reduced neck metastasis.

CONCLUSIONS

The effects of CCR5 antagonists in OSCC have been poorly studied, and this study reports in vitro and in vivo evidence for the effects of Maraviroc in OSCC. Our results suggest that the CCR5/CCL5 axis plays a role in oral cancer behavior, and that its inhibition is a promising new therapy alternative.

摘要

目的

CCR5/CCL5 轴对于恶性细胞与微环境成分之间的相互作用至关重要,促进了口腔鳞状细胞癌(OSCC)的肿瘤进展。本研究旨在评估 CCL5 和 CCR5 与口腔癌行为的关联,并评估 CCR5 拮抗剂的治疗潜力。

方法

进行了一项回顾性研究,以分析石蜡包埋组织中 CCR5 和 CCL5 的表达。在细胞系中,添加 rhCCL5 以诱导 CCR5 相关途径,并用 Maraviroc 和针对 CCR5 的 shRNA 中和受体。最后,使用舌癌的体内原位异种移植模型来评估 Maraviroc 作为肿瘤治疗。15 天后,处死小鼠,分析原发肿瘤和颈部淋巴结。

结果

CCR5 的表达与临床分期和转移有关,CCL5 与总生存期有关。添加 rhCCL5 诱导细胞增殖,而 shRNA 和 Maraviroc 以剂量依赖性方式降低其增殖。Maraviroc 治疗还增加了细胞凋亡并改变了细胞骨架组织。在体内,Maraviroc 减少了颈部转移。

结论

CCR5 拮抗剂在 OSCC 中的作用尚未得到充分研究,本研究报告了 Maraviroc 在 OSCC 中的体外和体内证据。我们的结果表明,CCR5/CCL5 轴在口腔癌行为中起作用,抑制该轴是一种有前途的新治疗选择。

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