Evidence map›Paper›PMID 26177060›Full record

ArticleCancer biology & therapy2015

Small molecule inhibitors of IRES-mediated translation.

Christos Vaklavas, Zheng Meng, Hyoungsoo Choi, William E Grizzle, Kurt R Zinn, Scott W Blume

Open access · hybridAbstract read
In one paragraph

Article in Cancer biology & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Current Practice in Bicistronic IRES Reporter Use: A Systematic Review.International journal of molecular sciences · 2021
    Pooled it
  2. Article
  3. IRES-Mediated Translation: Expanding the Toolkits of RNA Therapy.International journal of molecular sciences · 2025
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. IRES inhibition induces terminal differentiation and synchronized death in triple-negative breast cancer and glioblastoma cells.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
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

6 authors at 1 institution in 2 countries.

Christos Vaklavasa Comprehensive Cancer Center; University of Alabama at Birmingham ; Birmingham , AL USA.
Zheng Mengc Department of Biochemistry and Molecular Genetics; University of Alabama at Birmingham ; Birmingham , AL USA.
Hyoungsoo Choia Comprehensive Cancer Center; University of Alabama at Birmingham ; Birmingham , AL USA.
William E Grizzlea Comprehensive Cancer Center; University of Alabama at Birmingham ; Birmingham , AL USA.
Kurt R Zinna Comprehensive Cancer Center; University of Alabama at Birmingham ; Birmingham , AL USA.
Scott W Blumea Comprehensive Cancer Center; University of Alabama at Birmingham ; Birmingham , AL USA.
St. Vincent's Birmingham · US

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
Dysregulation of IGF-1R Translational ControlR01CA108886 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BLUME, SCOTT W · 2004 to 2015
$2.3M
NCI NIH HHS P30 CA013148NCI NIH HHS R01 CA108886NCI NIH HHS R01CA108886
6 · The paper itself

Abstract

Many genes controlling cell proliferation and survival (those most important to cancer biology) are now known to be regulated specifically at the translational (RNA to protein) level. The internal ribosome entry site (IRES) provides a mechanism by which the translational efficiency of an individual or group of mRNAs can be regulated independently of the global controls on general protein synthesis. IRES-mediated translation has been implicated as a significant contributor to the malignant phenotype and chemoresistance, however there has been no effective means by which to interfere with this specialized mode of protein synthesis. A cell-based empirical high-throughput screen was performed in attempt to identify compounds capable of selectively inhibiting translation mediated through the IGF1R IRES. Results obtained using the bicistronic reporter system demonstrate selective inhibition of second cistron translation (IRES-dependent). The lead compound and its structural analogs completely block de novo IGF1R protein synthesis in genetically-unmodified cells, confirming activity against the endogenous IRES. Spectrum of activity extends beyond IGF1R to include the c-myc IRES. The small molecule IRES inhibitor differentially modulates synthesis of the oncogenic (p64) and growth-inhibitory (p67) isoforms of Myc, suggesting that the IRES controls not only translational efficiency, but also choice of initiation codon. Sustained IRES inhibition has profound, detrimental effects on human tumor cells, inducing massive (>99%) cell death and complete loss of clonogenic survival in models of triple-negative breast cancer. The results begin to reveal new insights into the inherent complexity of gene-specific translational regulation, and the importance of IRES-mediated translation to tumor cell biology.

Indexed as

Cell ProliferationHumansInternal Ribosome Entry SitesProto-Oncogene Proteins c-mycTransfectionInternal Ribosome Entry SitesProto-Oncogene Proteins c-mycc-Mycgene-specific translational regulationIGF1RInternal ribosome entry site (IRES)triple-negative breast cancer

Identifiers

PMID26177060
PMCPMC4846101
OpenAlexW1030609836

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.