DDIT4/mTOR signaling pathway mediates cantharidin-induced hepatotoxicity and cellular damage

The molecular mechanism of CTD-induced toxicity in mouse liver and L-O2 cells is mainly through DDIT4/mTOR signaling pathway activation, leading to an increase in autophagy and apoptosis levels.

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Publication Details

Journal
Frontiers in Pharmacology
Published
2024-11-05
DOI
https://doi.org/10.3389/fphar.2024.1480512
Citations
2
Primary Topic
Beetle Biology and Toxicology Studies
Type
article
Field-Weighted Citation Impact
0.57

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article

DDIT4/mTOR signaling pathway mediates cantharidin-induced hepatotoxicity and cellular damage

Didong Lou, Qin Shi, Fang Peng, Can Zhu et al.
2 citations
Frontiers in Pharmacology
Beetle Biology and Toxicology Studies
0.57
article

DDIT4/mTOR signaling pathway mediates cantharidin-induced hepatotoxicity and cellular damage

Didong Lou, Qin Shi, Fang Peng, Can Zhu, Yue Pan, Wenchao Tang, Yuanyuan Xiao
article en
2 citations

Abstract

The molecular mechanism of CTD-induced toxicity in mouse liver and L-O2 cells is mainly through DDIT4/mTOR signaling pathway activation, leading to an increase in autophagy and apoptosis levels.

Frontiers in PharmacologyVol. 15
Guizhou University (CN)
National Natural Science Foundation of China, National Outstanding Youth Science Fund Project of National Natural Science Foundation of China
Good health and well-being
Openalex Percentile: Top 30%
Beetle Biology and Toxicology Studies
0.57
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DDIT4/mTOR signaling pathway mediates cantharidin-induced hepatotoxicity and cellular damage — Didong Lou, Qin Shi, et al. · Frontiers in Pharmacology (2024) | TGRS Research Map | TGRS