Evidence map›Paper›PMID 34511602›Full record

ArticleCell death & disease2021

EMP3 negatively modulates breast cancer cell DNA replication, DNA damage repair, and stem-like properties.

Kailing Zhou, Yu Sun, Dan Dong, Chenghai Zhao, Wei Wang

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

25 citing papers in PubMed, 36 citations in OpenAlex.

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  12. Epitranscriptomic RNA mAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
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  15. EMP3: A promising biomarker for tumor prognosis and targeted cancer therapy.Cancer biomarkers : section A of Disease markers · 2024
    Review
  16. Article
  17. Review
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  19. Recent Advances in RNA mCancer treatment and research · 2023
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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.

Kailing ZhouDepartment of Pathophysiology, College of Basic Medical Science, China Medical University, Shenyang, China.
Yu SunDepartment of Pathophysiology, College of Basic Medical Science, China Medical University, Shenyang, China.
Dan DongDepartment of Pathophysiology, College of Basic Medical Science, China Medical University, Shenyang, China.
Chenghai ZhaoDepartment of Pathophysiology, College of Basic Medical Science, China Medical University, Shenyang, China. chzhao@cmu.edu.cn.ORCID 0000-0003-2246-1425
Wei WangDepartment of Pathophysiology, College of Basic Medical Science, China Medical University, Shenyang, China. wangwei07@cmu.edu.cn.ORCID 0000-0001-5051-8594
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Enhanced DNA damage repair capacity attenuates cell killing of DNA-damaging chemotherapeutic agents. In silico analysis showed that epithelial membrane protein 3 (EMP3) is associated with favorable survival, and negatively regulates cell cycle S-phase. Consistently, loss and gain of function studies demonstrated that EMP3 inhibits breast cancer cell S-phage entry, DNA replication, DNA damage repair, and stem-like properties. Moreover, EMP3 blocks Akt-mTOR signaling activation and induces autophagy. EMP3 negatively modulates BRCA1 and RAD51 expression, indicating EMP3 suppresses homologous recombination repair of DNA double-strand breaks. Accordingly, EMP3 sensitizes breast cancer cells to the DNA-damaging drug Adriamycin. EMP3 downregulates YTHDC1, a RNA-binding protein involved in m6a modification, which at least in part mediates the effects of EMP3 on breast cancer cells. Taken together, these data indicate that EMP3 is a putative tumor suppressor in breast cancer, and EMP3 downregulation may be responsible for breast cancer chemoresistance.

Indexed as

DNA DamageDNA RepairDNA ReplicationAutophagyBreast NeoplasmsCell Line, TumorFemaleGene Expression Regulation, NeoplasticHistonesHumansMembrane GlycoproteinsModels, BiologicalNeoplasm ProteinsNeoplastic Stem CellsNerve Tissue ProteinsRNA Splicing FactorsEMP3 protein, humanH2AX protein, humanHistonesMembrane GlycoproteinsNeoplasm ProteinsNerve Tissue ProteinsRNA Splicing FactorsTumor Suppressor ProteinsYTHDC1 protein, human

Identifiers

PMID34511602
PMCPMC8435533
OpenAlexW3199017851

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.