Chronic stress disrupts hepatic homeostasis and accelerates liver cancer progression through ADRB2 signaling

Chronic stress has been implicated in the dysregulation of immunological, neurochemical, and endocrinological functions, yet its impact on hepatic homeostasis and liver carcinogenesis remains elusive. In this study, by using single-nucleus RNA sequencing and histopathological evaluation, we demonstrated that chronic stress induced profound hepatic dysfunction. Notably, using orthotopic murine models of liver cancer, we further found that chronic stress substantially accelerated tumor progression. Mechanistically, we identified β2-adrenergic receptor (ADRB2) signaling as the pivotal molecular pathway driving stress-accelerated cancer progression, which was in line with the poor clinical outcomes observed in patients with cancer exhibiting enhanced adrenergic signaling within tumors. Collectively, our study provides compelling evidence that chronic stress compromises hepatic homeostasis and accelerates liver cancer progression via ADRB2 activation, highlighting the therapeutic potential of targeting this pathway and the clinical importance of stress management in hepatic disorders.

Authors

Institutions

Publication Details

Journal
Science Advances
Published
2026-05-01
DOI
https://doi.org/10.1126/sciadv.aec0825
Primary Topic
Cancer, Stress, Anesthesia, and Immune Response
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Chronic stress disrupts hepatic homeostasis and accelerates liver cancer progression through ADRB2 signaling

Yue Lan, Ji Hu, Huimei Zhang, Li Li et al.
Science Advances
Cancer, Stress, Anesthesia, and Immune Response
article

Chronic stress disrupts hepatic homeostasis and accelerates liver cancer progression through ADRB2 signaling

Yue Lan, Ji Hu, Huimei Zhang, Li Li, Huimin Qin, Liuwei Chu, Xiaying Zheng
article en

Abstract

Chronic stress has been implicated in the dysregulation of immunological, neurochemical, and endocrinological functions, yet its impact on hepatic homeostasis and liver carcinogenesis remains elusive. In this study, by using single-nucleus RNA sequencing and histopathological evaluation, we demonstrated that chronic stress induced profound hepatic dysfunction. Notably, using orthotopic murine models of liver cancer, we further found that chronic stress substantially accelerated tumor progression. Mechanistically, we identified β2-adrenergic receptor (ADRB2) signaling as the pivotal molecular pathway driving stress-accelerated cancer progression, which was in line with the poor clinical outcomes observed in patients with cancer exhibiting enhanced adrenergic signaling within tumors. Collectively, our study provides compelling evidence that chronic stress compromises hepatic homeostasis and accelerates liver cancer progression via ADRB2 activation, highlighting the therapeutic potential of targeting this pathway and the clinical importance of stress management in hepatic disorders.

Science AdvancesVol. 12(18)
Shanghai Jiao Tong University (CN), ShanghaiTech University (CN), Second Affiliated Hospital of Guangzhou Medical University (CN), Shanghai Ninth People's Hospital (CN), Guangzhou First People's Hospital (CN), Guangzhou Medical University (CN)
Good health and well-being
Openalex Percentile: Top 10%
Cancer, Stress, Anesthesia, and Immune Response
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Chronic stress disrupts hepatic homeostasis and accelerates liver cancer progression through ADRB2 signaling — Yue Lan, Ji Hu, et al. · Science Advances (2026) | TGRS Research Map | TGRS