Evidence map›Paper›PMID 35327465›Full record

ArticleBiomedicines2022

Impact of

Shunichi Asai, Ayaka Koma, Nijiro Nohata, Takashi Kinoshita, Naoko Kikkawa, Mayuko Kato, Chikashi Minemura, Katsuhiro Uzawa, Toyoyuki Hanazawa, Naohiko Seki

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Shunichi AsaiDepartment of Functional Genomics, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.
Ayaka KomaDepartment of Oral Science, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Nijiro NohataMSD K.K., Tokyo 102-8667, Japan.ORCID 0000-0002-6816-2984
Takashi KinoshitaDepartment of Otorhinolaryngology/Head and Neck Surgery, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.
Naoko KikkawaDepartment of Functional Genomics, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.
Mayuko KatoDepartment of Functional Genomics, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.
Chikashi MinemuraDepartment of Oral Science, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.ORCID 0000-0001-8539-6240
Katsuhiro UzawaDepartment of Oral Science, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.ORCID 0000-0002-7036-0859
Toyoyuki HanazawaDepartment of Otorhinolaryngology/Head and Neck Surgery, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.ORCID 0000-0001-9721-5662
Naohiko SekiDepartment of Functional Genomics, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan.ORCID 0000-0003-4731-7956
Chiba University · JPMSD K.K. (Japan) · JP

Funding

JSPS KAKENHI 19K09863JSPS KAKENHI 19K18759JSPS KAKENHI 21K09577
6 · The paper itself

Abstract

Based on our original RNA sequence-based microRNA (miRNA) signatures of head and neck squamous cell carcinoma (HNSCC), it was revealed that the expression levels of miR-1-3p, miR-206, miR-133a-3p, and miR-133b were significantly suppressed in cancer specimens. Seed sequences of miR-1-3p/miR-206 and miR-133a-3p/miR-133b are identical. Interestingly, miR-1-3p/miR-133a-3p and miR-206/miR-133b are clustered in the human genome. We hypothesized that the genes coordinately controlled by these miRNAs are closely involved in the malignant transformation of HNSCC. Our in silico analysis identified a total of 28 genes that had putative miR-1-3p/miR-133a-3p and miR-206/miR-133b binding sites. Moreover, their expression levels were upregulated in HNSCC tissues. Multivariate Cox regression analyses showed that expression of PFN2 and PSEN1 were independent prognostic factors for patients with HNSCC (p < 0.05). Notably, four miRNAs (i.e., miR-1-3p, miR-206, miR-133a-3p, and miR-133b) directly bound the 3′untranslated region of PFN2 and controlled expression of the gene in HNSCC cells. Overexpression of PFN2 was confirmed in clinical specimens, and its aberrant expression facilitated cancer cell migration and invasion abilities. Our miRNA-based strategy continues to uncover novel genes closely involved in the oncogenesis of HNSCC.

Indexed as

clusteredHNSCCmicroRNAmiR-133a-3pmiR-133bmiR-1-3pmiR-206PFN2TCGA

Identifiers

PMID35327465
PMCPMC8944972
OpenAlexW4220908481

What OpenQuestion holds

Textmetadata
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.