Evidence map›Paper›PMID 29257343›Full record

ArticleMolecular medicine reports2018

Quantification of distinct let-7 microRNA family members by a modified stem-loop RT-qPCR.

Yilin Wang, Jianwen Zhou, Yanlian Chen, Chunhua Wang, Enyin Wu, Liang Fu, Chen Xie

Open access · bronzeAbstract read
In one paragraph

Article in Molecular medicine reports, 2018. 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
0.7field-weighted citation impact, top 33% 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, 21 citations in OpenAlex.

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  7. Cells · 2019
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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

7 authors at 5 institutions in 1 country.

Yilin Wang *Biochip Laboratory, Yantai Yuhuangding Hospital Affiliated to Qingdao University, Yantai, Shandong 264000, P.R. China.
Jianwen Zhou *Department of Pathology, First Affiliated Hospital, Sun Yat‑sen University, Guangzhou, Guangdong 510080, P.R. China.
Yanlian ChenKey Laboratory of Gene Engineering of The Ministry of Education, Cooperative Innovation Center for High Performance Computing, School of Life Sciences, Sun Yat‑sen University, Guangzhou, Guangdong 510006, P.R. China.
Chunhua WangBiochip Laboratory, Yantai Yuhuangding Hospital Affiliated to Qingdao University, Yantai, Shandong 264000, P.R. China.
Enyin WuBiochip Laboratory, Yantai Yuhuangding Hospital Affiliated to Qingdao University, Yantai, Shandong 264000, P.R. China.
Liang FuBiochip Laboratory, Yantai Yuhuangding Hospital Affiliated to Qingdao University, Yantai, Shandong 264000, P.R. China.
Chen XieShenzhen Weiguang Biological Products Co., Ltd., Shenzhen, Guangdong 518107, P.R. China.
Qingdao University · CNYuhuangding Hospital · CNShenzhen Weiguang Biological Products (China) · CNSun Yat-sen University · CNThe First Affiliated Hospital, Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lethal-7 (let-7) microRNA (miRNA) serves a pivotal role in a number of physiological processes and is associated with the occurrence and development of multiple disorders such as cancer. The present study aimed to use a newly developed stem‑loop strategy for reverse transcription‑quantitative polymerase chain reaction (RT‑qPCR) to distinguish let‑7 miRNA family members that differ by as little as a single nucleotide. For the miRNAs comprising 16 identical nucleotides at the 5'‑end, different stem‑loop RT primers were designed and used in RT‑qPCR to assess the expression profiles of a panel of let‑7 family member miRNAs in human glioblastoma U87 cells. Amplification efficiency was evaluated through correlation analysis between total RNA input and the quantification threshold values. Melting curve profiles were measured to estimate the amplification specificity of the improved stem‑loop RT‑qPCR compared with those of the poly(A)‑tailing method. In addition, the discrimination ability of the modified stem‑loop method was examined. Compared with poly(A) tailing, the modified stem‑loop RT method was able to specifically reverse transcribe the diverse let‑7 miRNA family members followed by accurate quantification, with a theoretical amplification efficiency of ~100%. This modified stem‑loop method was able to distinguish miRNAs with a single base difference. This innovative method may be used in the clinical detection of let‑7 expression levels in a variety of tumour samples, and may provide valuable data for disease diagnosis and prognostic evaluation. In addition, this method may offer a new avenue for developing particular stem‑loop approaches in measuring other miRNAs with little discrepancy.

Indexed as

Base SequenceCell Line, TumorDNA PrimersHumansMicroRNAsReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionDNA PrimersMicroRNAsmirnlet7 microRNA, humanlethal-7 familymicroRNAreverse transcription-quantitative polymerase chain reactionstem-loop primer

Identifiers

PMID29257343
PMCPMC5802175
OpenAlexW2781187978

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.