Evidence map›Paper›PMID 41001039›Full record

ArticleFrontiers in oncology2025

Securinine, a novel alkaloid, regulates cell cycle and EMT in gastric cancer by inducing iron-dependent cell death.

Weiwei Yuan, Hao Song, Yin Shi, Jianye Han, Shaohe Jiao, Song Liang, Yuanmin Xu, Yi Jiang, Yuehui Ji, Zhangming Chen and 3 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

13 authors.

Weiwei Yuan *Department of Thyroid Surgery, Baoshan Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Hao Song *Department of Internal Medicine, Yiwu Maternity and Children Hospital, Yiwu, China.
Yin Shi *Department of General Surgery, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Jianye HanDepartment of Internal Medicine, Yiwu Maternity and Children Hospital, Yiwu, China.
Shaohe JiaoDepartment of Internal Medicine, Yiwu Maternity and Children Hospital, Yiwu, China.
Song LiangDepartment of General Surgery, The Lu'an Affiliated Hospital of Anhui Medical University, Lu'an People's Hospital, Lu'an, China.
Yuanmin XuDepartment of Anesthesiology, The First Affiliated Hospital of University of Science and Technology of China, Division of Life Sciences and Medicine, Hefei, China.
Yi JiangNanjing University of Chinese Medicine, Nanjing, China.
Yuehui JiDepartment of General Surgery, The First People's Hospital of Wuhu, Wuhu, China.
Zhangming ChenDepartment of Internal Medicine, Yiwu Maternity and Children Hospital, Yiwu, China.
Limin LiuDepartment of Thyroid Surgery, Baoshan Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Aman XuDepartment of Internal Medicine, Yiwu Maternity and Children Hospital, Yiwu, China.
Zhou XuDepartment of Thyroid Surgery, Baoshan Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Gastric cancer remains one of the most prevalent and lethal cancers worldwide, with its insidious onset hindering early diagnosis and effective treatment. Despite advances, the overall survival rate for gastric cancer remains low, primarily due to late diagnosis, tumor heterogeneity, and resistance to current therapies. This highlights the urgent need for novel therapeutic strategies. Methods: Gastric cancer cell lines were treated with securinine, followed by analysis of cell proliferation, cycle, and Epithelial-Mesenchymal Transition (EMT) using Western blot and immunofluorescence techniques. Transcriptomic analysis was performed to identify changes in ferroptosis-related iron metabolism pathways. Results: Securinine significantly inhibited proliferation and modulated the cell cycle, arresting cells at the G2/M transition, while also enhancing EMT, which altered cell migration and invasiveness. Transcriptomic analysis revealed that securinine activated ferroptosis-related iron metabolic pathways, upregulating key genes such as HMOX1, FTH1, and FTR. Inhibition of these genes reversed the effects on cell proliferation and EMT, highlighting the role of ferroptosis in the anticancer effects of securinine. Conclusions: Securinine shows potential as a novel therapeutic agent for gastric cancer by inducing ferroptosis and modulating key cell death and survival pathways. Its ability to regulate iron metabolism and EMT suggests that it could be a promising candidate for developing new therapeutic strategies against gastric cancer, especially for drug-resistant cases.

Indexed as

epithelial-mesenchymal transitiongastric canceriron metabolism pathwayssecurininetumor cell cycle

Identifiers

PMID41001039
PMCPMC12457131

What OpenQuestion holds

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Registered trials

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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.