Evidence map›Paper›PMID 35041678›Full record

ArticlePloS one

Curcumin suppresses tumorigenesis by ferroptosis in breast cancer.

Xuelei Cao, Yao Li, Yongbin Wang, Tao Yu, Chao Zhu, Xuezhi Zhang, Jialiang Guan

Open access · goldAbstract read
In one paragraph

Article in PloS one. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 1 pooled it
14.3field-weighted citation impact, top 1% 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

63 citing papers in PubMed, 1 synthesis or guideline pooled it, 97 citations in OpenAlex.

  1. Pooled it
  2. Circular RNAs in ferroptosis regulation and tumor progression of gynecological and breast cancers: molecular mechanisms and therapeutic potential.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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3 more citing papers are in PubMed but not listed here.

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

7 authors at 1 institution in 1 country.

Xuelei CaoThe Department of Emergency Internal Medicine, the Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Yao LiThe Department of Nephrology, the Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Yongbin WangThe Department of Emergency Internal Medicine, the Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Tao YuThe Department of Emergency Internal Medicine, the Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Chao ZhuThe Department of Clinical Laboratory, the Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Xuezhi ZhangThe Department of Cardiology, the Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Jialiang GuanThe Department of Emergency Internal Medicine, the Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.ORCID https://orcid.org/0000-0003-2608-2449
Qingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer (BC) is one of the most common malignant tumors found in females. Previous studies have demonstrated that curcumin, which is a type of polyphenol compound extracted from Curcuma longa underground rhizome, is able to inhibit the survival of cancer cells. However, the functional role and mechanism of curcumin in BC are still unclear. The Cell Counting Kit-8 assay was performed to examine the effects of curcumin on cell viability in the BC cell lines MDA-MB-453 and MCF-7. The levels of lipid reactive oxygen species (ROS), malondialdehyde (MDA) production, and intracellular Fe2+ were determined to assess the effects of curcumin on cell ferroptosis. Western blot analysis was also carried out to detect the protein levels. Finally, the antitumorigenic effect of curcumin on BC was identified in a xenograft tumor model. In the present study, the results indicated that curcumin could dose-dependently suppress the viability of both MDA-MB-453 and MCF-7 cells. Further studies revealed that curcumin facilitated solute carrier family 1 member 5 (SLC1A5)-mediated ferroptosis in both MDA-MB-453 and MCF-7 cells by enhancing lipid ROS levels, lipid peroxidation end-product MDA accumulation, and intracellular Fe2+ levels. In vivo experiments demonstrated that curcumin could significantly hamper tumor growth. Collectively, the results demonstrated that curcumin exhibited antitumorigenic activity in BC by promoting SLC1A5-mediated ferroptosis, which suggests its use as a potential therapeutic agent for the treatment of BC.

Indexed as

Breast NeoplasmsCurcuminFerroptosisReactive Oxygen SpeciesXenograft Model Antitumor AssaysAmino Acid Transport System y+AnimalsCarcinogenesisCell Line, TumorCell SurvivalFemaleHumansLipid PeroxidationMCF-7 CellsMiceMice, Inbred BALB CAmino Acid Transport System y+CurcuminReactive Oxygen Species

Identifiers

PMID35041678
PMCPMC8765616
OpenAlexW4206353619

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.