Evidence map›Paper›PMID 29509055›Full record

ArticleCancer biology & therapy2018

MiR-422a weakened breast cancer stem cells properties by targeting PLP2.

Yanmei Zou, Yuandong Chen, Shuo Yao, Guangrui Deng, Dian Liu, Xun Yuan, Shunfang Liu, Jie Rao, Huihua Xiong, Xianglin Yuan and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

30 citing papers in PubMed, 35 citations in OpenAlex.

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  13. Processing body (P-body) and its mediators in cancer.Molecular and cellular biochemistry · 2022
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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

14 authors at 2 institutions in 2 countries.

Yanmei Zoua Department of Oncology , Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology , Wuhan , Hubei , China.
Yuandong Chenb Department of Oncology , Huangzhou District People's Hospital , Huanggang , Hubei , China.
Shuo Yaoa Department of Oncology , Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology , Wuhan , Hubei , China.
Guangrui Dengb Department of Oncology , Huangzhou District People's Hospital , Huanggang , Hubei , China.
Dian Liua Department of Oncology , Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology , Wuhan , Hubei , China.
Xun Yuana Department of Oncology , Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology , Wuhan , Hubei , China.
Shunfang Liua Department of Oncology , Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology , Wuhan , Hubei , China.
Jie Raoa Department of Oncology , Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology , Wuhan , Hubei , China.
Huihua Xionga Department of Oncology , Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology , Wuhan , Hubei , China.
Xianglin Yuana Department of Oncology , Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology , Wuhan , Hubei , China.
Shiying Yua Department of Oncology , Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology , Wuhan , Hubei , China.
Feng Zhud Department of Biochemistry and Molecular Biology , School of Basic Medicine, Huazhong University of Science and Technology , Wuhan , Hubei , China.
Yihua Wanga Department of Oncology , Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology , Wuhan , Hubei , China.
Hua Xionga Department of Oncology , Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology , Wuhan , Hubei , China.
Tongji Hospital · CNHuanggang Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study investigated miR-422a and PLP2 expressions in breast cancer cells and breast cancer stem cells (BCSCs). Besides, their influences on polymorphism changes were observed.

methodsFlow cytometry and fluorescence-activated cell sorting was performed and CD24

resultsBMSCs were successfully established from MCF7 cells and miR-422a expression was downregulated while PLP2 level decreased in BMSCs. MiR-422a directly targets the 3'UTR of PLP2 and suppressed its expression. Besides, the up-regulation of miR-422a contributed to weakened ability of proliferation and microsphere formation of BMSCs, while PLP2 overexpression facilitated those biological abilities. Tumorigenesis of BMSCs in mice models was impaired by either overexpression of miR-442a or silencing of PLP2.

conclusionUp-regulation of miR-422a attenuated microsphere formation, proliferation and tumor formation of breast cancer stem cells via suppressing the PLP2 expression.

Indexed as

AnimalsBreast NeoplasmsCell Line, TumorFemaleHeterograftsHumansMARVEL Domain-Containing ProteinsMCF-7 CellsMice, Inbred NODMice, SCIDMicroRNAsNeoplastic Stem CellsProteolipidsTransfectionMARVEL Domain-Containing ProteinsMicroRNAsMIRN422 microRNA, humanPLP2 protein, humanProteolipidsbreast cancer stem cellsmiR-422aPLP2

Identifiers

PMID29509055
PMCPMC5915044
OpenAlexW2793646920

What OpenQuestion holds

Textmetadata
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.