Evidence map›Paper›PMID 32594835›Full record

ArticleCell cycle (Georgetown, Tex.)2020

Low expression of miR-let-7a promotes cell growth and invasion through the regulation of c-Myc in oral squamous cell carcinoma.

Chunyang Luo, Jiyong Zhang, Yi Zhang, Xiao Zhang, Yinan Chen, Weimin Fan

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 24% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Pooled it
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  11. MicroRNA-124-3p-enriched small extracellular vesicles as a therapeutic approach for Parkinson's disease.Molecular therapy : the journal of the American Society of Gene Therapy · 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

6 authors at 1 institution in 1 country.

Chunyang LuoDepartment of Orthopaedics, The First Affiliated Hospital of Nanjing Medical University , Nanjing, China.ORCID 0000-0002-1232-1974
Jiyong ZhangDepartment of Orthopaedics, The First Affiliated Hospital of Nanjing Medical University , Nanjing, China.
Yi ZhangDepartment of Orthopaedics, The First Affiliated Hospital of Nanjing Medical University , Nanjing, China.
Xiao ZhangDepartment of Orthopaedics, The First Affiliated Hospital of Nanjing Medical University , Nanjing, China.
Yinan ChenDepartment of Anesthesiology, The First Affiliated Hospital of Nanjing Medical University , Nanjing, China.
Weimin FanDepartment of Orthopaedics, The First Affiliated Hospital of Nanjing Medical University , Nanjing, China.
Jiangsu Province Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In oral squamous cell carcinoma (OSCC), abnormal expression of microRNAs has been extensively reported. MiR-let-7a has been validated as a critical regulator of multiple cancers, but the biological process involved and its potential role in OSCC remain unknown.We first analyzed the differential expression of miR-let-7a in cancer tissues, adjacent noncancerous tissues and cell lines. The functional role of miR-let-7a in OSCC cell lines was evaluated by using colony formation assays, cell proliferation and transwell invasion assays in vitro. In addition, subcutaneous xenotransplantation of miR-let-7a transfected cells into nude mouse model was carried out to explore the potential function of miR-let-7a in vivo.miR-let-7a levels were found to be significantly downregulated in OSCC tissues compared with matched normal tissues (n = 60), and lower expression of miR-let-7a was related to poor prognosis in OSCC patients. Overexpression of MiR-let-7a induced a suppression in proliferation, invasion and migration and inhibited tumourigenesis in the nude mouse model. We also determined that c-Myc may serve as a direct target of miR-let-7a; furthermore, upregulated c-Myc expression could partially rescue the effects caused by miR-let-7a overexpression. miR-let-7a is low expression in OSCC, and promotes tumor development by directly targeting c-Myc. Our results may provide a potential therapeutic role for miR-let-7a in human OSCC.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsBase SequenceCarcinoma, Squamous CellCell Line, TumorCell MovementCell ProliferationDown-RegulationFemaleHumansMaleMAP Kinase Signaling SystemMice, Inbred BALB CMice, NudeMicroRNAsMiddle AgedMicroRNAsmirnlet7 microRNA, humanProto-Oncogene Proteins c-mycinvasionmigrationmiR-let-7aOSCCproliferation

Identifiers

PMID32594835
PMCPMC7469679
OpenAlexW3037157877

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.