Evidence map›Paper›PMID 40394754›Full record

ArticleJournal of cellular and molecular medicine2025

Erk1/2 Orchestrates SSPH I-Induced Oxidative Stress, Mitochondrial Dysfunction and Ferroptosis in Hepatocellular Carcinoma.

Yuewen Sun, Ying Zhou, Dan Huang, Zhiguang Zhao, Qingrui Shao, Jianzhe Li, Xiaofang Zhao, Xudong Liu

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Haemolytic injury and cardiovascular disease.Nature reviews. Cardiology · 2026
    Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Yuewen SunGuangxi University of Chinese Medicine, Nanning, China.ORCID 0000-0002-7235-6802
Ying ZhouGuangxi University of Chinese Medicine, Nanning, China.
Dan HuangGuangxi Vocational University of Agriculture, Nanning, China.
Zhiguang ZhaoYunnan Grassroots Medical Industry Development Co. Ltd, Kunming, China.
Qingrui ShaoGuangxi University of Chinese Medicine, Nanning, China.
Jianzhe LiGuangxi University of Chinese Medicine, Nanning, China.
Xiaofang ZhaoGuangxi University of Chinese Medicine, Nanning, China.
Xudong LiuGuangxi University of Chinese Medicine, Nanning, China.

Funding

National Natural Science Foundation of China 82060793Natural Science Foundation of Guangxi Province 2021JJB140005Qihuang Project Team of Guangxi University of Chinese Medicine 2021007Young talents in Gui Pai Xing lin of Guangxi University of Chinese Medicine 2022C043
6 · The paper itself

Abstract

Although Erk1/2 has been linked to oxidative stress regulation in hepatocellular carcinoma (HCC), the interplay among Erk1/2, reactive oxygen species (ROS), and iron metabolism remains poorly characterised. The steroidal saponin SSPH I, a recognised ferroptosis inducer, exerts dual pharmacological effects via Erk1/2 and ROS-dependent pathways. This study aimed to investigate the regulatory mechanisms of Erk1/2 in ferroptosis and oxidative stress and analyse their feedback regulatory effects on Erk1/2 in HCC using SSPH I as a pharmacological probe, and further elucidate the anti-HCC effects and mechanisms of SSPH I in vitro and in vivo. Mechanistic studies utilised three inhibitors: U0126 (Erk1/2 phosphorylation inhibitor), Ferrostatin-1 (ferroptosis inhibitor), and N-acetyl cysteine (ROS scavenger), combined with SSPH I to delineate its effects on cell viability, mitochondrial dynamics, ferroptosis induction and oxidative stress. Mechanistically, SSPH I disrupted mitochondrial function and suppressed HCC cell survival through iron accumulation and ROS generation, while concurrently activating Erk1/2 signalling. Pharmacological inhibition of ROS or iron pathways partially attenuated SSPH I-induced ferroptosis and ROS generation, but failed to abrogate these effects. Erk1/2 inhibition completely abolished SSPH I-mediated regulation of the Nrf1/2-HO-1 axis and ferroptosis-related protein expression in cellular and animal models, identifying Erk1/2 as the upstream regulatory node. Notably, while both SSPH I and U0126 monotherapies inhibited xenograft growth, their combined use resulted in antagonistic effects. These findings establish Erk1/2 activation as the central molecular mechanism orchestrating SSPH I-driven oxidative stress amplification, mitochondrial dysfunction and ferroptosis execution in HCC.

Indexed as

Carcinoma, HepatocellularFerroptosisLiver NeoplasmsMAP Kinase Signaling SystemMitochondriaOxidative StressSaponinsAnimalsButadienesCell Line, TumorCell SurvivalHumansIronMiceMice, NudeNitrilesButadienesIronNitrilesReactive Oxygen SpeciesSaponinsU 0126Erk1/2ferroptosisNrf1/2ROSSSPH I

Identifiers

PMID40394754
PMCPMC12092237

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.