Evidence map›Paper›PMID 19524505›Full record

ArticleCell2009

Therapeutic microRNA delivery suppresses tumorigenesis in a murine liver cancer model.

Janaiah Kota, Raghu R Chivukula, Kathryn A O'Donnell, Erik A Wentzel, Chrystal L Montgomery, Hun-Way Hwang, Tsung-Cheng Chang, Perumal Vivekanandan, Michael Torbenson, K Reed Clark and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 879 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
879citing papers in PubMed, 2 pooled it
59.7field-weighted citation impact, top 1% 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

879 citing papers in PubMed, 2 syntheses or guidelines pooled it, 1,708 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. p27 Expression in Wild-Type KRAS Colon Cancer.Journal of cellular and molecular medicine · 2026
    Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Non-coding RNAs in alcohol-associated liver disease.Liver research (Beijing, China) · 2025
    Review
  16. Article
  17. Targeted Cancer Stem Cell Therapeutics: An Update.Current topics in medicinal chemistry · 2025
    Review
  18. Review
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 1 country.

Janaiah KotaCenter for Gene Therapy, The Research Institute at Nationwide Children's Hospital, Columbus, OH 43205, USA.
Raghu R Chivukula
Kathryn A O'Donnell
Erik A Wentzel
Chrystal L Montgomery
Hun-Way Hwang
Tsung-Cheng Chang
Perumal Vivekanandan
Michael Torbenson
K Reed Clark
Jerry R Mendell
Joshua T Mendell
Johns Hopkins Medicine · USJohns Hopkins University · USNationwide Children's Hospital · USHigh Throughput Biology (United States) · USThe Ohio State University · US

Funding

c-Myc-regulated microRNAs in normal and pathologic cellular physiologyR01CA120185 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MENDELL, JOSHUA T · 2007 to 2015
$2.5M
NCI NIH HHS R01 CA120185
6 · The paper itself

Abstract

Therapeutic strategies based on modulation of microRNA (miRNA) activity hold great promise due to the ability of these small RNAs to potently influence cellular behavior. In this study, we investigated the efficacy of a miRNA replacement therapy for liver cancer. We demonstrate that hepatocellular carcinoma (HCC) cells exhibit reduced expression of miR-26a, a miRNA that is normally expressed at high levels in diverse tissues. Expression of this miRNA in liver cancer cells in vitro induces cell-cycle arrest associated with direct targeting of cyclins D2 and E2. Systemic administration of this miRNA in a mouse model of HCC using adeno-associated virus (AAV) results in inhibition of cancer cell proliferation, induction of tumor-specific apoptosis, and dramatic protection from disease progression without toxicity. These findings suggest that delivery of miRNAs that are highly expressed and therefore tolerated in normal tissues but lost in disease cells may provide a general strategy for miRNA replacement therapies.

Indexed as

AnimalsCarcinoma, HepatocellularCyclin D2CyclinsDependovirusDisease Models, AnimalGenetic VectorsLiver NeoplasmsMiceMicroRNAsProto-Oncogene Proteins c-mycCCND2 protein, humanCCNE2 protein, humanCyclin D2CyclinsMicroRNAsMIRN26 microRNA, humanMYC protein, humanProto-Oncogene Proteins c-myc

Identifiers

PMID19524505
PMCPMC2722880
OpenAlexW2159807040

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.