← 返回前沿论文

神经递质降钙素基因相关肽在甲状腺髓样癌中塑造免疫抑制微环境

英文原题:The neurotransmitter calcitonin gene-related peptide shapes an immunosuppressive microenvironment in medullary thyroid cancer.

PubMed 2024/07/19(内容时间) Nat Commun Q1 · IF 18.1(JCR 2025)

研究概要

我们的研究提供了对MTC免疫抑制微环境的见解,并提出CGRP受体作为潜在的治疗靶点。

中文摘要

神经递质是神经免疫回路中的关键调节因子,并与肿瘤进展相关。甲状腺髓样癌(MTC)是一种侵袭性神经内分泌肿瘤,表达神经递质降钙素基因相关肽(CGRP),对化疗和放疗不敏感,免疫疗法的有效性尚不清楚。因此,对肿瘤微环境的全面分析将有助于有效治疗,并为CGRP在神经系统外的功能提供证据。在此,我们比较了MTC和甲状腺乳头状癌(PTC)的单细胞图谱,发现MTC中CGRP的表达与树突状细胞(DC)异常发育相关,其特征为cAMP相关通路的激活和高水平的Kruppel样因子2(KLF2),并与肿瘤浸润T细胞活性受损相关。CGRP受体拮抗剂可以在体外抵消CGRP对DC发育的不利影响。我们的研究提供了对MTC免疫抑制微环境的见解,并提出CGRP受体作为潜在的治疗靶点。

展开英文摘要原文

Neurotransmitters are key modulators in neuro-immune circuits and have been linked to tumor progression. Medullary thyroid cancer (MTC), an aggressive neuroendocrine tumor, expresses neurotransmitter calcitonin gene-related peptide (CGRP), is insensitive to chemo- and radiotherapies, and the effectiveness of immunotherapies remains unknown. Thus, a comprehensive analysis of the tumor microenvironment would facilitate effective therapies and provide evidence on CGRP's function outside the nervous system. Here, we compare the single-cell landscape of MTC and papillary thyroid cancer (PTC) and find that expression of CGRP in MTC is associated with dendritic cell (DC) abnormal development characterized by activation of cAMP related pathways and high levels of Kruppel Like Factor 2 (KLF2), correlated with an impaired activity of tumor infiltrating T cells. A CGRP receptor antagonist could offset CGRP detrimental impact on DC development in vitro. Our study provides insights of the MTC immunosuppressive microenvironment, and proposes CGRP receptor as a potential therapeutic target.

论文信息

作者
Hou Y、Lin B、Xu T、Jiang J、Luo S、Chen W、Chen X、Wang Y
第一作者单位
Department of Endocrinology, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.China
通讯作者单位
Department of Endocrinology, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China. xiaohp@mail.sysu.edu.cn.China
文献类型
非美国政府资助研究
期刊
Nature communications2024 Jul 19
原文标识
PubMed 39030177 · DOI 10.1038/s41467-024-49824-7