Evidence map›Paper›PMID 31101802›Full record

ArticleCell death & disease2019

MALAT1 regulates miR-34a expression in melanoma cells.

Fei Li, Xinji Li, Li Qiao, Wen Liu, Chengshan Xu, Xiaogang Wang

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.9field-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

34 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
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  7. Heliyon · 2023
    Review
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  9. Frontiers in genetics · 2023
    Article
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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

6 authors at 3 institutions in 1 country.

Fei LiDepartment of Dermatology, Air Force Medical Center, PLA, Beijing, China. leefei@126.com.
Xinji LiDepartment of Radiation Oncology, Air Force Medical Center, PLA, Beijing, China.
Li QiaoDepartment of Dermatology, Air Force Medical Center, PLA, Beijing, China.
Wen LiuDepartment of Dermatology, Air Force Medical Center, PLA, Beijing, China.
Chengshan XuNational Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology, Beijing, China.
Xiaogang WangBeijing Advanced Innovation Center for Big Data-based Precision Medicine, Beihang University, Beijing, China. xiaogangwang@buaa.edu.cn.
Air Force General Hospital PLA · CNBeihang University · CNBeijing Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanoma is one of the most common skin malignancies. Both microRNAs and long non-coding RNAs (lncRNAs) have critical roles in the progression of cancers, including melanoma. However, the underlying molecular mechanism has not been fully characterized. We demonstrated that miR-34a is negatively correlated with MALAT1 in melanoma cells and tumor specimens. Interestingly, MALAT1, which contains functional sequence-specific miR-34a-binding sites, regulates miR-34a stability in melanoma cells and in vivo. Importantly, MALAT1 was significantly enriched in the Ago2 complex, but not when the MALAT1-binding site of miR-34a was mutated. Furthermore, MALAT1 could be shown to regulate c-Myc and Met expression by functioning as a miR-34a sponge. Our results reveal an unexpected mode of action for MALAT1 as an important regulator of miR-34a.

Indexed as

Amino Acid SequenceAnimalsAntagomirsArgonaute ProteinsBinding SitesCell Line, TumorHumansMaleMelanomaMiceMice, NudeMicroRNAsMutagenesisProto-Oncogene Proteins c-metProto-Oncogene Proteins c-mycRNA InterferenceAGO2 protein, humanAntagomirsArgonaute ProteinsMALAT1 long non-coding RNA, humanMET protein, humanMicroRNAsMIRN34 microRNA, humanMYC protein, humanProto-Oncogene Proteins c-metProto-Oncogene Proteins c-mycRNA, Long NoncodingRNA, Small Interfering

Identifiers

PMID31101802
PMCPMC6525244
OpenAlexW2945922564

What OpenQuestion holds

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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.