Evidence map›Paper›PMID 30729639›Full record

ReviewCancer science2019

Development of miRNA-based therapeutic approaches for cancer patients.

Ryou-U Takahashi, Marta Prieto-Vila, Isaku Kohama, Takahiro Ochiya

Abstract 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 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
–field-weighted citation impact
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

73 citing papers in PubMed.

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13 more citing papers are in PubMed but not listed here.

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

4 authors.

Ryou-U TakahashiDivision of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.
Marta Prieto-VilaDivision of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.
Isaku KohamaDivision of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.
Takahiro OchiyaDivision of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0002-0776-9918

Funding

Japan Agency for Medical Research and DevelopmentJapan Society for the Promotion of Science C/16K08261
6 · The paper itself

Abstract

Over the past few decades, siRNA and miRNA have attracted a great deal of attention from researchers and clinicians. These molecules have been extensively studied from the standpoint of developing biopharmaceuticals against various diseases, including heart disease, diabetes and cancers. siRNA suppresses only a single target, whereas each miRNA regulates the expression of multiple target genes. More importantly, because miRNA are also secreted from cancer cells, and their aberrant expression is associated with tumor development and progression, they represent not only therapeutic targets but also promising biomarkers for diagnosis and prognosis. Therefore, miRNA may be more effective tools against cancers, in which multiple signal pathways are dysregulated. In this review, we summarize recent progress in the development of miRNA therapeutics for the treatment of cancer patients, and describe delivery systems for oligonucleotide therapeutics.

Indexed as

Gene Expression Regulation, NeoplasticRNA InterferenceRNAi TherapeuticsAnimalsAntineoplastic AgentsBiomarkers, TumorCell Transformation, NeoplasticDrug Resistance, NeoplasmEpithelial-Mesenchymal TransitionGene Transfer TechniquesHumansMicroRNAsNeoplasm MetastasisNeoplasmsRNA, MessengerAntineoplastic AgentsBiomarkers, TumorMicroRNAsRNA, Messengercancer biologydelivery systemexosomesmiRNAtherapeutics

Identifiers

PMID30729639
PMCPMC6447849

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Registered trials

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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.