Evidence map›Paper›PMID 26256260›Full record

ReviewJournal of controlled release : official journal of the Controlled Release Society2015

Small molecules targeting microRNA for cancer therapy: Promises and obstacles.

Di Wen, Michael Danquah, Amit Kumar Chaudhary, Ram I Mahato

Abstract readReview
In one paragraph

Review in Journal of controlled release : official journal of the Controlled Release Society, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

61 citing papers in PubMed, 97 citations in OpenAlex.

  1. Review
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  5. Article
  6. Unraveling LncRNAs: the future of lung cancer treatment.Journal of the Egyptian National Cancer Institute · 2025
    Review
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  18. Targeting non-coding RNAs to overcome cancer therapy resistance.Signal transduction and targeted therapy · 2022
    Review
  19. Article
  20. Article

1 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 at 2 institutions in 1 country.

Di WenDepartment of Pharmaceutical Sciences, University of Nebraska Medical Center, 986025 Nebraska Medical Center, Omaha, NE 68198-6025, USA.
Michael DanquahDepartment of Pharmaceutical Sciences, Chicago State University, 9501 South King Drive., Chicago, IL 60628, USA.
Amit Kumar ChaudharyDepartment of Pharmaceutical Sciences, University of Nebraska Medical Center, 986025 Nebraska Medical Center, Omaha, NE 68198-6025, USA.
Ram I MahatoDepartment of Pharmaceutical Sciences, University of Nebraska Medical Center, 986025 Nebraska Medical Center, Omaha, NE 68198-6025, USA. Electronic address: ram.mahato@unmc.edu.
Nebraska Medical Center · USChicago State University · US

Funding

UNMC/EPPLEY CANCER CENTER SUPPORT GRANTP30CA036727 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Apar Kishor Ganti · 1985 to 2026
$55.0M
Polymeric Nanomedicines of Hedgehog Inhibitor and miRNA for Treating Pancreatic CancerR01GM113166 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BATRA, SURINDER K., MAHATO, RAM I. · 2015 to 2018
$1.4M
Polymeric Nanomedicines of Small Molecules and miRNA for Treating Pancreatic CancR01EB017853 · NIBIB · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI MAHATO, RAM I. · 2014 to 2017
$1.4M
NCI NIH HHS P30 CA036727NCI NIH HHS P30CA036727NIBIB NIH HHS 1R01EB017853NIBIB NIH HHS R01 EB017853NIGMS NIH HHS 1R01GM113166NIGMS NIH HHS R01 GM113166
6 · The paper itself

Abstract

Aberrant expression of miRNAs is critically implicated in cancer initiation and progression. Therapeutic approaches focused on regulating miRNAs are therefore a promising approach for treating cancer. Antisense oligonucleotides, miRNA sponges, and CRISPR/Cas9 genome editing systems are being investigated as tools for regulating miRNAs. Despite the accruing insights in the use of these tools, delivery concerns have mitigated clinical application of such systems. In contrast, little attention has been given to the potential of small molecules to modulate miRNA expression for cancer therapy. In these years, many researches proved that small molecules targeting cancer-related miRNAs might have greater potential for cancer treatment. Small molecules targeting cancer related miRNAs showed significantly promising results in different cancer models. However, there are still several obstacles hindering the progress and clinical application in this area. This review discusses the development, mechanisms and application of small molecules for modulating oncogenic miRNAs (oncomiRs). Attention has also been given to screening technologies and perspectives aimed to facilitate clinical translation for small molecule-based miRNA therapeutics.

Indexed as

MicroRNAsAnimalsHumansMolecular Targeted TherapyNeoplasmsMicroRNAsCancer therapymiRNAOncomiRSmall molecule miRNA inhibitors

Identifiers

PMID26256260
PMCPMC4749151
OpenAlexW1907037111

What OpenQuestion holds

Textmetadata
LicenceTDM
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.