Evidence map›Paper›PMID 33168512›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2018

[MiR-433 reverses chemoresistance to docetaxel by targeting Notch1 in breast cancer cells].

Xiaolei Hu, Pingmei Huang, Jie Wang, Wan He, Pan Zhao, Guangyu Yao, Changsheng Ye

Abstract readEnglish Abstract
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 2 institutions in 1 country.

Xiaolei HuBreast Center, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Pingmei HuangBreast Center, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Jie WangDepartment of Clinical Nutrition, 458 Hospital of PLA, Guangzhou 510602, China.
Wan HeDepartment of Oncology, Shenzhen People's Hospital, Second Clinical Medical College of Jinan University, Shenzhen 518020, China.
Pan ZhaoClinical Medical Research Center, Shenzhen People's Hospital, Second Clinical Medical College of Jinan University, Shenzhen 518020, China.
Guangyu YaoBreast Center, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Changsheng YeBreast Center, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Nanfang Hospital · CNSouthern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the role of miR- 433 in chemoresistance to docetaxel in breast cancer cells.

methodsA docetaxel-resistant MCF-7 breast cancer cell line (MCF-7/DOX) was established by exposure of parental MCF-7 cells to progressively increased docetaxel concentrations. The functional role of miR-433 was investigated by assessing the changes in viability and apoptosis of the cells transfected with a miR-433 inhibitor or a miR-433 mimics. The downstream targets of miR- 433 were determined by bioinformatics analysis, cell transfection and luciferase reporter assay.

resultsQuantitative real-time PCR analysis showed that miR- 433 was down-regulated in MCF-7/DOX cells. Transfection of the cells with the miR-433 inhibitor obviously enhanced chemoresistance to docetaxel and attenuated cell apoptosis in MCF-7 cells; miR-433 overexpression significantly increased the sensitivity to docetaxel and promoted apoptosis in MCF- 7/DOX cells. Luciferase reporter assay showed that the down-regulation miR-433 expression was associated with significantly increased expressions of Notch1 at both mRNA and protein levels in MCF-7 cells. Compared with the control cells, McF-7/DOX cells transfected with miR-433 mimics exhibited significantly decreased mRNA and protein expressions of Notch1.

conclusionsmiR-433 may reverse chemoresistance to docetaxel by targeting Notch1 in breast cancer cells.

Indexed as

breast cancerchemoresistancedocetaxelMCF-7miR-433Notch1

Identifiers

PMID33168512
PMCPMC6765539
OpenAlexW3103784177

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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.