Evidence map›Paper›PMID 36814470›Full record

ArticleEvidence-based complementary and alternative medicine : eCAM2023

Curcumin Analog, HO-3867, Induces Both Apoptosis and Ferroptosis via Multiple Mechanisms in NSCLC Cells with Wild-Type p53.

Ling Wu, Guodong Xu, Ni Li, Linwen Zhu, Guofeng Shao

Open access · hybridAbstract read
In one paragraph

Article in Evidence-based complementary and alternative medicine : eCAM, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 3% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

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  8. Research Progress of Regulatory Cell Death in Coronary Microembolization.International journal of medical sciences · 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.

Ling WuSchool of Medicine, Ningbo University, Ningbo, Zhejiang 315211, China.ORCID https://orcid.org/0000-0002-5464-5918
Guodong XuDepartment of Cardiothoracic Surgery, Lihuili Hospital Affiliated to Ningbo University, Ningbo, Zhejiang 315000, China.ORCID https://orcid.org/0000-0001-8684-6485
Ni LiDepartment of Cardiothoracic Surgery, Lihuili Hospital Affiliated to Ningbo University, Ningbo, Zhejiang 315000, China.ORCID https://orcid.org/0000-0002-1747-665X
Linwen ZhuDepartment of Cardiothoracic Surgery, Lihuili Hospital Affiliated to Ningbo University, Ningbo, Zhejiang 315000, China.ORCID https://orcid.org/0000-0002-6210-9816
Guofeng ShaoDepartment of Cardiothoracic Surgery, Lihuili Hospital Affiliated to Ningbo University, Ningbo, Zhejiang 315000, China.ORCID https://orcid.org/0000-0002-6980-2752
Ningbo University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over the last decade, researchers have paid more and more attention to the natural compound curcumin for its potential application in anticancer therapy. However, the application of curcumin has been limited owing to its rapid metabolism in the body. HO-3867, a stable curcumin analog, shows potent antitumor activities against various tumor cells. Yet, information on HO-3867's impact on non-small-cell lung cancer (NSCLC) cells is lacking. Herein, we evaluated the cytotoxicity of HO-3867 in NSCLC cells. We discovered that HO-3867 suppressed the viability of NSCLC cells containing wild-type p53. In NSCLC cells, HO-3867 promotes both apoptosis and ferroptosis, the latter of which is a newly discovered mode of cell death. Mechanically, HO-3867-induced apoptosis relied on the inhibition of Mcl-1 and Bcl-2 and the upregulation of Bax. Moreover, NSCLC cells undergo ferroptosis when treated with HO-3867 via activating the p53-DMT1 axis and suppressing GPX4. Additionally, HO-3867 caused an accumulation of reactive oxygen species (ROS) in NSCLC in a way that was dependent on the presence of iron. Our findings point to the possibility that HO-3867 might be employed as a therapeutic agent for treating NSCLC.

Identifiers

PMID36814470
PMCPMC9940973
OpenAlexW4320480573

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.