文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

芳烃受体作为肿瘤调节因子:治疗机制

The aryl hydrocarbon receptor as a tumor modulator: mechanisms to therapy.

作者信息

Chaudhry Kanita A, Bianchi-Smiraglia Anna

机构信息

Department of Cell Stress Biology, Roswell Park Comprehensive Cancer Center, Buffalo, New York, NY, United States.

出版信息

Front Oncol. 2024 May 14;14:1375905. doi: 10.3389/fonc.2024.1375905. eCollection 2024.


DOI:10.3389/fonc.2024.1375905
PMID:38807762
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11130384/
Abstract

The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor that is widely recognized to play important, but complex, modulatory roles in a variety of tumor types. In this review, we comprehensively summarize the increasingly controversial role of AhR as a tumor regulator and the mechanisms by which it alters tumor progression based on the cancer cell type. Finally, we discuss new and emerging strategies to therapeutically modulate AhR, focusing on novel agents that hold promise in current human clinical trials as well as existing FDA-approved drugs that could potentially be repurposed for cancer therapy.

摘要

芳基烃受体(AhR)是一种配体激活的转录因子,人们普遍认为它在多种肿瘤类型中发挥着重要但复杂的调节作用。在本综述中,我们全面总结了AhR作为肿瘤调节因子这一日益具有争议性的作用,以及它根据癌细胞类型改变肿瘤进展的机制。最后,我们讨论了治疗性调节AhR的新出现的策略,重点关注在当前人类临床试验中具有前景的新型药物以及可能被重新用于癌症治疗的现有FDA批准药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73ea/11130384/9a0b712bcdf2/fonc-14-1375905-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73ea/11130384/90e8df0d9e81/fonc-14-1375905-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73ea/11130384/f68367bd088c/fonc-14-1375905-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73ea/11130384/9a0b712bcdf2/fonc-14-1375905-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73ea/11130384/90e8df0d9e81/fonc-14-1375905-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73ea/11130384/f68367bd088c/fonc-14-1375905-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73ea/11130384/9a0b712bcdf2/fonc-14-1375905-g003.jpg

相似文献

[1]
The aryl hydrocarbon receptor as a tumor modulator: mechanisms to therapy.

Front Oncol. 2024-5-14

[2]
Single Nucleotide Polymorphisms at a Distance from Aryl Hydrocarbon Receptor (AHR) Binding Sites Influence AHR Ligand-Dependent Gene Expression.

Drug Metab Dispos. 2019-7-10

[3]
Interactions of the aryl hydrocarbon receptor with inflammatory mediators: beyond CYP1A regulation.

Curr Drug Metab. 2011-2

[4]
The Aryl Hydrocarbon Receptor and Tumor Immunity.

Front Immunol. 2018-2-13

[5]
The aryl hydrocarbon receptor (AhR) in the regulation of cell-cell contact and tumor growth.

Carcinogenesis. 2010-1-27

[6]
Activation of aryl hydrocarbon receptor signaling by gallic acid suppresses progression of human breast cancer in vitro and in vivo.

Phytomedicine. 2022-2

[7]
Aryl hydrocarbon receptor, cell cycle regulation, toxicity, and tumorigenesis.

J Cell Biochem. 2005-12-15

[8]
The effects of environmental aryl hydrocarbon receptor ligands on signaling and cell metabolism in cancer.

Biochem Pharmacol. 2023-10

[9]
Cell-intrinsic view of the aryl hydrocarbon receptor in tumor immunity.

Trends Immunol. 2022-3

[10]
Aryl hydrocarbon receptor as a drug target in advanced prostate cancer therapy - obstacles and perspectives.

Transcription. 2025-2

引用本文的文献

[1]
Immunometabolism of Innate Immune Cells in Gastrointestinal Cancer.

Cancers (Basel). 2025-4-27

[2]
Unveiling the Immune effects of AHR in tumors: a decade of insights from bibliometric analysis (2010-2023).

Discov Oncol. 2024-11-4

[3]
Vulnerability of Antioxidant Drug Therapies on Targeting the Nrf2-Trp53-Jdp2 Axis in Controlling Tumorigenesis.

Cells. 2024-10-3

[4]
A reference for selecting an appropriate method for generating glioblastoma organoids from the application perspective.

Discov Oncol. 2024-9-18

本文引用的文献

[1]
Targeting aryl hydrocarbon receptor to prevent cancer in barrier organs.

Biochem Pharmacol. 2024-5

[2]
Aryl hydrocarbon receptor suppresses STING-mediated type I IFN expression in triple-negative breast cancer.

Sci Rep. 2024-3-8

[3]
The Aryl Hydrocarbon Receptor: Impact on the Tumor Immune Microenvironment and Modulation as a Potential Therapy.

Cancers (Basel). 2024-1-23

[4]
ARID5A stabilizes Indoleamine 2,3-dioxygenase expression and enhances CAR T cell exhaustion in colorectal cancer.

Transl Oncol. 2024-4

[5]
Aryl hydrocarbon receptor is a tumor promoter in -amplified neuroblastoma cells through suppression of differentiation.

iScience. 2023-10-21

[6]
Targeting the aryl hydrocarbon receptor (AhR) with BAY 2416964: a selective small molecule inhibitor for cancer immunotherapy.

J Immunother Cancer. 2023-11

[7]
The aryl hydrocarbon receptor maintains antitumor activity of liver resident natural killer cells after partial hepatectomy in C57BL/6J mice.

Cancer Med. 2023-10

[8]
The tryptophan-kynurenine pathway in immunomodulation and cancer metastasis.

Cancer Med. 2023-9

[9]
Modulation of T cells by tryptophan metabolites in the kynurenine pathway.

Trends Pharmacol Sci. 2023-7

[10]
Dietary tryptophan metabolite released by intratumoral Lactobacillus reuteri facilitates immune checkpoint inhibitor treatment.

Cell. 2023-4-27

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

推荐工具

医学文档翻译智能文献检索