Evidence map›Paper›PMID 37047300›Full record

ArticleInternational journal of molecular sciences2023

Different miRNAs Related to

Ho Suk Kang, Ha Young Park, Hyun Lim, Il Tae Son, Min-Jeong Kim, Nan Young Kim, Min Jeong Kim, Eun Sook Nam, Seong Jin Cho, Mi Jung Kwon

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 45% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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 4 institutions in 1 country.

Ho Suk KangDepartment of Internal Medicine, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang 14068, Republic of Korea.
Ha Young ParkDepartment of Pathology, Busan Paik Hospital, Inje University College of Medicine, Busan 47392, Republic of Korea.
Hyun LimDepartment of Internal Medicine, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang 14068, Republic of Korea.
Il Tae SonDepartment of Surgery, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang 14068, Republic of Korea.
Min-Jeong KimDepartment of Radiology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang 14068, Republic of Korea.ORCID 0000-0002-7484-5896
Nan Young KimHallym Institute of Translational Genomics and Bioinformatics, Hallym University Medical Center, Anyang 14068, Republic of Korea.ORCID 0000-0001-9245-8657
Min Jeong KimDepartment of Surgery, Kangdong Sacred Heart Hospital, Seoul 05355, Republic of Korea.
Eun Sook NamDepartment of Pathology, Kangdong Sacred Heart Hospital, Seoul 05355, Republic of Korea.
Seong Jin ChoDepartment of Pathology, Kangdong Sacred Heart Hospital, Seoul 05355, Republic of Korea.
Mi Jung KwonDepartment of Pathology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang 14068, Republic of Korea.ORCID 0000-0002-2441-0448
Hallym University Sacred Heart Hospital · KRKangdong Sacred Heart Hospital · KRHallym University Medical Center · KRInje University Busan Paik Hospital · KR

Funding

National Research Foundation of Korea grant no. NRF-2022R1F1A1065335
6 · The paper itself

Abstract

Recent studies suggest that miRNA may be involved in the development of rectal neuroendocrine tumors (NETs). We explored the frequency of clinicopathologically relevant mutations and miRNA expression in rectal NETs to examine molecular profiles related to prognosis and behavior. Twenty-four eligible specimens with endoscopically excised rectal NETs were selected. Next-generation sequencing and an miRNA expression assay were used to evaluate the expression profile relevant to common genetic mutations in rectal NETs. Kyoto Encyclopedia of Genes and Genomes analysis predicted that the possible target signaling pathways were correlated with dysregulated miRNAs. Nineteen rectal NETs harbored more than one mutation in the 24 cancer-related genes. Seven miRNAs (hsa-miR-769-5p, hsa-miR-221-3p, hsa-miR-34a-5p, hsa-miR-181c-5p, hsa-miR-1246, hsa-miR-324-5p, and hsa-miR-361-3p) were significantly down-regulated in tumors harboring the

Indexed as

MicroRNAsNeuroendocrine TumorsF-Box-WD Repeat-Containing Protein 7Gene Expression ProfilingHumansMitotic IndexMutationPilot ProjectsF-Box-WD Repeat-Containing Protein 7FBXW7 protein, humanMicroRNAsMIRN324 microRNA, humanFBXW7miR-3934-5pmiR-769-5pmiRNAsneuroendocrine tumorrectum

Identifiers

PMID37047300
PMCPMC10093831
OpenAlexW4361224450

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.