Evidence map›Paper›PMID 31187550›Full record

ReviewCancer science2019

Significant epitranscriptomes in heterogeneous cancer.

Masamitsu Konno, Masateru Taniguchi, Hideshi Ishii

Open access · goldAbstract readReview
In one paragraph

Review in Cancer science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 24 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

3 authors at 3 institutions in 1 country.

Masamitsu KonnoDepartment of Frontier Science for Cancer and Chemotherapy, Graduate School of Medicine, Osaka University, Osaka, Japan.ORCID https://orcid.org/0000-0001-6960-2315
Masateru TaniguchiThe Institute of Scientific and Industrial Research, Osaka University, Osaka, Japan.
Hideshi IshiiDepartment of Medical Data Science, Graduate School of Medicine, Osaka University, Osaka, Japan.
Osaka City University · JPOsaka Research Institute of Industrial Science and Technology · JPThe University of Osaka · JP

Funding

Japan Agency for Medical Research and DevelopmentJapan Society for the Promotion of Science 16K15615Japan Society for the Promotion of Science 17H04282Japan Society for the Promotion of Science 17K19698
6 · The paper itself

Abstract

Precision medicine places significant emphasis on techniques for the identification of DNA mutations and gene expression by deep sequencing of gene panels to obtain medical data. However, other diverse information that is not easily readable using bioinformatics, including RNA modifications, has emerged as a novel diagnostic and innovative therapy owing to its multifunctional aspects. It is suggested that this breakthrough innovation might open new avenues for the elucidation of uncharacterized cancer cellular functions to develop more precise medical applications. The functional characteristics and regulatory mechanisms of RNA modifications, ie, the epitranscriptome (ETR), which reflects RNA metabolism, remains unclear, mainly due to detection methods being limited. Recent studies have revealed that N6-methyl adenosine, the most common modification in mRNA in eukaryotes, is affected in various types of cancer and, in some cases, cancer stem cells, but also affects cellular responses to viral infections. The ETR can control cancer cell fate through mRNA splicing, stability, nuclear export, and translation. Here we report on the recent progress of ETR detection methods, and biological findings regarding the significance of ETR in cancer precision medicine.

Indexed as

AdenosineAnimalsEukaryotaHumansNeoplasmsPrecision MedicineRNA, MessengerTranscriptomeAdenosineN-methyladenosineRNA, MessengerdiagnosismodificationMODOMICSRNAtherapy

Identifiers

PMID31187550
PMCPMC6676114
OpenAlexW2952708223

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.