Evidence map›Paper›PMID 36503456›Full record

ArticleAnti-cancer agents in medicinal chemistry2024

Arnicolide D Inhibits Oxidative Stress-induced Breast Cancer Cell Growth and Invasion through Apoptosis, Ferroptosis, and Parthanatos.

Wei Wen, Ke Jin, Ying Che, Lin-Yao Du, Li-Na Wang

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Article in Anti-cancer agents in medicinal chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 32% of its field
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

10 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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  3. Molecules (Basel, Switzerland) · 2025
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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

5 authors at 1 institution in 1 country.

Wei WenGeneral Surgery Department, The First Affiliated Hospital of Dalian Medical University, Dalian, 116011, China.ORCID 0000-0002-1030-5911
Ke JinEmergency Department, The second Affiliated Hospital of Dalian Medical University, Dalian, 116023, China.
Ying CheUltrasonic Diagnostics Department, The First Affiliated Hospital of Dalian Medical University, Dalian, 116011, China.
Lin-Yao DuUltrasonic Diagnostics Department, The First Affiliated Hospital of Dalian Medical University, Dalian, 116011, China.
Li-Na WangUltrasonic Diagnostics Department, The First Affiliated Hospital of Dalian Medical University, Dalian, 116011, China.
Dalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer is the most common malignant tumor in women, and its pathogenesis is very complicated. More and more studies have found that Traditional Chinese Medicine plays an important role in tumor prevention.

objectiveTo investigate the mechanism of arnicolide D isolated from Centipeda minima in breast cancer.

methodsCell Counting Kit-8 (CCK-8), western blot, RT-qPCR, ELISA, flow cytometry, and Transwell were used to detect the effect of arnicolide D on the biological function of breast cancer cells.

resultsArnicolide D promoted reactive oxygen species (ROS) production and induced a decrease in mitochondrial membrane potential in breast cancer cells, thereby inhibiting cell viability and increasing lactate dehydrogenase (LDH) release. Arnicolide D activated the classical apoptosis pathway to induce cell apoptosis; it significantly promoted PARP-1 expression, enhanced the nuclear translocation of apoptosis-inducing factor (AIF), and reduced the expression of AIF in mitochondria, indicating that it can induce the occurrence of parthanatos in a ROS dependent manner. In addition, arnicolide D down-regulated glutathione peroxidase 4 (GPX4) expression and increased the accumulation of Fe

conclusionArnicolide D can activate a variety of cell death modes by inducing oxidative stress, thereby inhibiting the growth and invasion of breast cancer cells, indicating that arnicolide D has a good anti-tumor effect.

Indexed as

ApoptosisBreast NeoplasmsCell ProliferationFerroptosisOxidative StressAntineoplastic AgentsCell SurvivalDose-Response Relationship, DrugDrug Screening Assays, AntitumorFemaleHumansMolecular StructureReactive Oxygen SpeciesSesquiterpenesStructure-Activity RelationshipTumor Cells, CulturedAntineoplastic AgentsReactive Oxygen SpeciesSesquiterpenesarnicolide DBreast cancerchinese medicinal herbferroptosisparthanatosreactive oxygen species (ROS).

Identifiers

PMID36503456
OpenAlexW4311206015

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.