Evidence map›Paper›PMID 31120927›Full record

ArticlePloS one2019

Norcantharidin regulates ERα signaling and tamoxifen resistance via targeting miR-873/CDK3 in breast cancer cells.

Xiumei Zhang, Bingfeng Zhang, Panhong Zhang, Lihui Lian, Lianlian Li, Zhihong Qiu, Kai Qian, An Chen, Qiongqing Liu, Yinjie Jiang and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 28% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

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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

12 authors at 2 institutions in 1 country.

Xiumei ZhangThe Center for Translational Medicine, Yichun University, Yichun, Jiangxi, P.R. China.
Bingfeng ZhangCollege of Chemistry and Bio-engineering, Yichun University, Yichun, Jiangxi, P.R. China.
Panhong ZhangThe Center for Translational Medicine, Yichun University, Yichun, Jiangxi, P.R. China.
Lihui LianDepartment of Cell Biology, College of Life Sciences, Shandong First Medical University & Shandong Academy of Medical Sciences, Taian, Shandong, P.R. China.
Lianlian LiThe Center for Translational Medicine, Yichun University, Yichun, Jiangxi, P.R. China.
Zhihong QiuThe Center for Translational Medicine, Yichun University, Yichun, Jiangxi, P.R. China.
Kai QianThe Center for Translational Medicine, Yichun University, Yichun, Jiangxi, P.R. China.
An ChenThe Center for Translational Medicine, Yichun University, Yichun, Jiangxi, P.R. China.
Qiongqing LiuThe Center for Translational Medicine, Yichun University, Yichun, Jiangxi, P.R. China.
Yinjie JiangThe Center for Translational Medicine, Yichun University, Yichun, Jiangxi, P.R. China.
Jiajun CuiThe Center for Translational Medicine, Yichun University, Yichun, Jiangxi, P.R. China.ORCID 0000-0002-9000-371X
Bing QiDepartment of Cell Biology, College of Life Sciences, Shandong First Medical University & Shandong Academy of Medical Sciences, Taian, Shandong, P.R. China.
Yichun University · CNShandong First Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MiR-873/CDK3 has been shown to play a critical role in ERα signaling and tamoxifen resistance. Thus, targeting this pathway may be a potential therapeutic approach for the treatment of ER positive breast cancer especially tamoxifen resistant subtype. Here we report that Norcantharidin (NCTD), currently used clinically as an ani-cancer drug in China, regulates miR-873/CDK3 axis in breast cancer cells. NCTD decreases the transcriptional activity of ERα but not ERβ through the modulation of miR-873/CDK3 axis. We also found that NCTD inhibits cell proliferation and tumor growth and miR-873/CDK3 axis mediates cell proliferation suppression of NCTD. More important, we found that NCTD sensitizes resistant cells to tamoxifen. NCTD inhibits tamoxifen induced the transcriptional activity as well ERα downstream gene expressions in tamoxifen resistant breast cancer cells. In addition, we found that NCTD restores tamoxifen induced recruitments of ERα co-repressors N-CoR and SMRT. Knockdown of miR-873 and overexpression of CDK3 diminish the effect of NCTD on tamoxifen resistance. Our data shows that NCTD regulates ERα signaling and tamoxifen resistance by targeting miR-873/CDK3 axis in breast cancer cells. This study may provide an alternative therapy strategy for tamoxifen resistant breast cancer.

Indexed as

AnimalsAntineoplastic AgentsAntineoplastic Agents, HormonalApoptosisBreast NeoplasmsBridged Bicyclo Compounds, HeterocyclicCell ProliferationCyclin-Dependent Kinase 3Drug Resistance, NeoplasmEstrogen Receptor alphaFemaleGene Expression Regulation, NeoplasticHumansMiceMice, NudeMicroRNAsAntineoplastic AgentsAntineoplastic Agents, HormonalBridged Bicyclo Compounds, HeterocyclicCDK3 protein, humanCyclin-Dependent Kinase 3ESR1 protein, humanEstrogen Receptor alphaMicroRNAsMIRN873 microRNA, humannorcantharidinTamoxifen

Identifiers

PMID31120927
PMCPMC6532885
OpenAlexW2945497192

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.