Polycyclic aromatic hydrocarbons promote tumorigenesis of gallbladder cancer via aryl hydrocarbon Receptor-HEGBC positive feedback axis

被引:0
作者
Yuan, Lei [1 ]
Zhang, Yumeng [2 ]
Xu, Jianguo [3 ]
Liu, Feng [4 ]
Liang, Yingchao [2 ]
Wang, Beili [2 ]
Wu, Meihong [5 ]
Fan, Zhiyuan [6 ]
Yang, Liang [1 ,2 ]
机构
[1] Quzhou Peoples Hosp, Dept Hepatobiliary Surg, 100 Minjiang Main Rd, Quzhou 324000, Zhejiang, Peoples R China
[2] Tongji Univ, Shanghai Matern & Infant Hosp 1, Sch Med, Dept Radiat Oncol, Shanghai 201204, Peoples R China
[3] Naval Med Univ, Changhai Hosp, Dept Plast Surg, Shanghai 200433, Peoples R China
[4] Novel Intel Biotech Nanjing Co Ltd, Dept Sci Res, Nanjing 211899, Peoples R China
[5] Naval Med Univ, Changhai Hosp, Dept Oncol, Shanghai 200433, Peoples R China
[6] Tongji Univ, Shanghai Matern & Infant Hosp 1, Sch Med, Dept Breast Surg, Shanghai 201204, Peoples R China
基金
中国国家自然科学基金;
关键词
RNA; AHR; RISK; TRANSCRIPTION; PROMISCUITY; ACTIVATION; MECHANISMS; BINDING;
D O I
10.1016/j.isci.2025.112505
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Gallbladder cancer (GBC) is a highly aggressive tumor associated with risk factors, such as chronic infection, gallstones, and exposure to harmful chemicals. Our study explores the role of polycyclic aromatic hydrocarbons (PAHs) and long noncoding RNA HEGBC in GBC progression. We found that PAHs activate the aryl hydrocarbon receptor (AhR), which enhances HEGBC expression and promotes GBC cell proliferation, invasion, and metastasis both in vitro and in vivo. Mechanistically, AhR binds to the HEGBC promoter, establishing a positive feedback loop that further activates AhR transcription. Moreover, CYP1A1 was identified as a key downstream effector of PAHs-AhR/HEGBC-mediated proliferation, migration, and invasion of GBC cells in vitro and in vivo. These findings provide the integrative view of a molecular mechanism loop for regulating the malignant progression of GBC centered by PAHs/AhR/HEGBC, which represents a promising strategy for the treatment of GBC.
引用
收藏
页数:21
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