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首页|期刊导航|中国免疫学杂志|miR-4738-3p靶向TDO2调控能量代谢抑制甲状腺癌细胞免疫逃逸的作用

miR-4738-3p靶向TDO2调控能量代谢抑制甲状腺癌细胞免疫逃逸的作用

刘臻臻 宋远鹏 张雪琳 何英 郑小东

中国免疫学杂志2025,Vol.41Issue(11):2637-2644,8.
中国免疫学杂志2025,Vol.41Issue(11):2637-2644,8.DOI:10.3969/j.issn.1000-484X.2025.11.014

miR-4738-3p靶向TDO2调控能量代谢抑制甲状腺癌细胞免疫逃逸的作用

Role of miR-4738-3p targeting TDO2 in regulating energy metabolism and inhibiting immune escape of thyroid cancer cells

刘臻臻 1宋远鹏 1张雪琳 1何英 1郑小东1

作者信息

  • 1. 首都医科大学附属北京安贞医院南充医院暨南充市中心医院/川北医学院第二临床医学院乳腺甲状腺血管外科,南充 637000
  • 折叠

摘要

Abstract

Objective:To investigate role of miR-4738-3p in targeting tryptophan 2,3-dioxygenase 2(TDO2)to regulate energy metabolism and inhibit immune escape in thyroid cancer cells.Methods:A total of 68 cases of thyroid cancer tissues and their corresponding adjacent non-cancerous tissues were collected,expressions of miR-4738-3p and TDO2 in tissues and cell lines were de-tected by qRT-PCR,relationship between miR-4738-3p expression and clinicopathological characteristics was analyzed.Effects of miR-4738-3p and TDO2 on proliferation,migration,invasion,energy metabolism and immune escape of TPC-1 and BCPAP cells were examined through CCK-8,clone formation,wound healing,Transwell experiments,biochemical analyses,ELISA and NK cell co-culture experiments,targeting relationship between miR-4738-3p and TDO2 was validated by dual luciferase reporter gene assay.In vivo xenograft experiments and immunohistochemical detections were conducted to observe effects of miR-4738-3p on tumorigenesis and expression of immune escape-related proteins in TPC-1 and BCPAP cells.Results:miR-4738-3p was lowly expressed(P<0.05),while TDO2 was highly expressed in thyroid cancer(P<0.05).Tumor size,lymph node metastasis and TNM staging were correlated with expression of miR-4738-3p(P<0.05).Compared with miR-NC group,miR-4738-3p mimics group exhibited decreased prolifera-tion,clone formation,migration,invasion ability,glucose uptake,lactate production,ATP/ADP ratio,TDO2 mRNA and protein expressions,tumor volume,mass,Ki-67,TDO2 and PD-L1 expressions(P<0.05),NAD+/NADH ratio,IFN-γ,TNF-α levels and NK cell killing rate were increased(P<0.05).miR-4738-3p inhibitor group showed increased proliferation,clone formation,migration,invasion ability,glucose uptake,lactate production,ATP/ADP ratio,TDO2 mRNA and protein expressions(P<0.05),NAD+/NADH ratio,IFN-γ,TNF-α levels and NK cell killing rate were decreased(P<0.05).Binding sites were identified between miR-4738-3p and TDO2,and their expression were negatively correlated(r=-0.485 3,P<0.001).Compared with sh-NC group,proliferation,clone formation,migration,invasion ability,glucose uptake,lactate production and ATP/ADP ratio were decreased in sh-TDO2 group(P<0.05),NAD+/NADH ratio,IFN-γ,TNF-α levels and NK cell killing rate were increased(P<0.05).Compared with Scrambled group,proliferation,clone formation,migration,invasion ability,glucose uptake,lactate production and ATP/ADP ratio were increased in TDO2 group(P<0.05),NAD+/NADH ratio,IFN-γ,TNF-α levels and NK cell killing rate were decreased(P<0.05).Conclusion:miR-4738-3p targets TDO2 to regulate energy metabolism,inhibiting thyroid cancer cell proliferation,metastasis and immune escape.

关键词

miR-4738-3p/色氨酸2,3-加双氧酶2/甲状腺癌/能量代谢/免疫逃逸

Key words

miR-4738-3p/Tryptophan 2,3-dioxygenase 2/Thyroid cancer/Energy metabolism/Immune escape

分类

临床医学

引用本文复制引用

刘臻臻,宋远鹏,张雪琳,何英,郑小东..miR-4738-3p靶向TDO2调控能量代谢抑制甲状腺癌细胞免疫逃逸的作用[J].中国免疫学杂志,2025,41(11):2637-2644,8.

中国免疫学杂志

OA北大核心

1000-484X

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