Evidence map›Paper›PMID 35410813›Full record

ArticleBiomedical journal2021

LncRNA MALAT1 promotes breast cancer progression and doxorubicin resistance via regulating miR-570-3p.

Xin Yue, Wen-Ying Wu, Ma Dong, Meng Guo

Open access · goldAbstract read
In one paragraph

Article in Biomedical journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 8% 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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

  1. Multilevel Mechanisms of Cancer Drug Resistance.International journal of molecular sciences · 2024
    Pooled it
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  6. Longitudinal tracking ofMolecular therapy. Oncology · 2025
    Article
  7. Non-coding RNAs modulation in breast cancer radioresponse: mechanisms and therapeutic implications.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2025
    Review
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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

4 authors at 4 institutions in 1 country.

Xin YueDepartment of Breast Surgery, The First People's Hospital of Jingzhou, Jingzhou, China.
Wen-Ying WuInterventional Operating Room of the Department of Radiology, The First Affiliated Hospital of China Medical University, Shenyang, China.
Ma DongDepartment of Radiology, Liaoning Cancer Hospital, Shenyang, China.
Meng GuoDepartment of Surgery of Mammary Gland and Thyroid Gland, Jining No.1 People's Hospital, Affiliated Jining No.1 Hospital of Jining Medical University, Jining, China. Electronic address: mguomeng@126.com.
Affiliated Hospital of Jining Medical University · CNChina Medical University · CNFirst People's Hospital of Jingzhou · CNLiaoning Cancer Hospital & Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetastasis-associated lung adenocarcinoma transcript 1 (MALAT1) is a long non-coding RNA (lncRNA) that regulates disease progression in various types of cancers. The aim of this study was to explore the role of MALAT1 in breast cancer (BC) progression and doxorubicin resistance.

methodsReal-time polymerase chain reaction (RT-PCR) was used to determine the expression of MALAT1 in BC tissues and cells; MTT and Transwell assay were used to detect the proliferation, migration and invasion of BC cells, respectively; drug resistance test was performed to assess the sensitivity of BC cells to doxorubicin; dual-luciferase reporter gene assay was conducted to verify the interaction between MALAT1 and miR-570-3p.

resultsMALAT1 was highly expressed in BC tissues compared with normal tissues adjacent to cancer as well as in BC cells. In addition, inhibition the expression of MALAT1 could significantly suppress the proliferation, migration and invasion of BC cells. Meanwhile, down-regulation of MALAT1 sensitized BC cells to doxorubicin. Moreover, bioinformatics analysis suggested that miR-570-3p was the potential downstream target of MALAT1. Dual-luciferase reporter gene assay confirmed that MALAT1 could directly target miR-570-3p. Additionally, miR-570-3p was lowly expressed in BC tissues and cells. Up-regulation of miR-570-3p not only significantly inhibited the proliferation, metastasis, and invasion of BC cells, but also increased the sensitivity of BC cells to doxorubicin.

conclusionMALAT1 functions as a novel oncogenic lncRNA in regulating the progression and doxorubicin resistance of BC by targeting miR-570-3p.

Indexed as

Breast NeoplasmsLung NeoplasmsMicroRNAsRNA, Long NoncodingCell Line, TumorCell ProliferationDoxorubicinFemaleGene Expression Regulation, NeoplasticHumansDoxorubicinMicroRNAsMIRN570 microRNA, humanRNA, Long NoncodingBreast cancerLong non-coding RNAMetastasis-associated lung adenocarcinoma transcript 1miR-570–3p

Identifiers

PMID35410813
PMCPMC9068547
OpenAlexW3096514992

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.