Evidence map›Paper›PMID 30013364›Full record

ArticleOncoTargets and therapy2018

miR-106b-5p inhibits the invasion and metastasis of colorectal cancer by targeting CTSA.

Shujuan Ni, Weiwei Weng, Midie Xu, Qifeng Wang, Cong Tan, Hui Sun, Lei Wang, Dan Huang, Xiang Du, Weiqi Sheng

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

40 citing papers in PubMed, 53 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.

Shujuan Ni *Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China, shengweiqi2006@163.com.
Weiwei Weng *Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China, shengweiqi2006@163.com.
Midie XuDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China, shengweiqi2006@163.com.
Qifeng WangDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China, shengweiqi2006@163.com.
Cong TanDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China, shengweiqi2006@163.com.
Hui SunDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China, shengweiqi2006@163.com.
Lei WangDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China, shengweiqi2006@163.com.
Dan HuangDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China, shengweiqi2006@163.com.
Xiang DuDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China, shengweiqi2006@163.com.
Weiqi ShengDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China, shengweiqi2006@163.com.
Fudan University Shanghai Cancer Center · CNShanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough miR-106b-5p has been reported to play a pivotal role in various human malignancies, its role in colorectal cancer (CRC) remains unknown. In this study, we comprehensively investigated miR-106b-5p expression and biologic functions in CRC and the molecular mechanism involved. PATIENTS AND

methodsmiR-106b-5p expression was detected in CRC tissues and cell lines by quantitative reverse transcription-polymerase chain reaction. The effects of miR-106b-5p on metastasis were determined in vitro using transwell assays, and in vivo effects were evaluated using a mouse tail vein injection model. Downstream targets of miR-106b-5p were confirmed using bioinformatics programs, luciferase assays, and rescue experiments. Target gene expression and clinicopathologic parameters were also analyzed.

resultsmiR-106b-5p expression was lower in CRC tissues than in corresponding nontumorous tissues (

conclusionOur findings revealed that miR-106b-5p inhibits CRC metastasis by upregulating CTSA expression, which may lead to novel therapeutic strategies for CRC patients.

Indexed as

cathepsin Acolorectal cancermetastasismiR-106b-5p

Identifiers

PMID30013364
PMCPMC6038879
OpenAlexW2809714622

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.