Evidence map›Paper›PMID 19454272›Full record

ReviewExperimental and molecular pathology2009

Discovery and development of the G-rich oligonucleotide AS1411 as a novel treatment for cancer.

Paula J Bates, Damian A Laber, Donald M Miller, Shelia D Thomas, John O Trent

Open access · greenAbstract readReview
In one paragraph

Review in Experimental and molecular pathology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 351 papers.

0numbers the graph read from it
0cells of the map it votes in
351citing papers in PubMed
12.4field-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

351 citing papers in PubMed, 839 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Advances in Aptamer Drug Delivery Systems for Treatment of Glioblastoma.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  5. Review
  6. Article
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  9. Article
  10. Review
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  17. Modulating a Massive Set of Biomolecular Structures by Sono-Mechanical Force.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  18. Synthetic short RNA in cancer.Frontiers in oncology · 2026
    Review
  19. Review
  20. Article

291 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

5 authors at 2 institutions in 1 country.

Paula J BatesJames Graham Brown Cancer Center, Department of Medicine, University of Louisville, Louisville, Kentucky 40202, USA. paula.bates@louisville.edu
Damian A Laber
Donald M Miller
Shelia D Thomas
John O Trent
University of Louisville · USJames Graham Brown Foundation · US

Funding

Tumor-Targeting OligonucleotidesR01CA122383 · NCI · UNIVERSITY OF LOUISVILLE · PI BATES, PAULA J. · 2006 to 2010
$1.3M
Development of Nucleolin targeted Anticancer CompoundsR01CA113735 · NCI · UNIVERSITY OF LOUISVILLE · PI TRENT, JOHN O · 2005 to 2009
$1.3M
Nucleolin--A Novel Target for Cancer Drug DiscoveryR21CA091115 · NCI · UNIVERSITY OF LOUISVILLE · PI BATES, PAULA J · 2001 to 2002
$288k
A Role for Nucleolin in Malignant Transformation?R21CA104230 · NCI · UNIVERSITY OF LOUISVILLE · PI BATES, PAULA J · 2004 to 2005
$265k
NCI NIH HHS R01 CA113735NCI NIH HHS R01 CA122383NCI NIH HHS R21 CA091115NCI NIH HHS R21 CA104230NCI NIH HHS R21 CA91115
6 · The paper itself

Abstract

Certain guanine-rich (G-rich) DNA and RNA molecules can associate intermolecularly or intramolecularly to form four stranded or "quadruplex" structures, which have unusual biophysical and biological properties. Several synthetic G-rich quadruplex-forming oligodeoxynucleotides have recently been investigated as therapeutic agents for various human diseases. We refer to these biologically active G-rich oligonucleotides as aptamers because their activities arise from binding to protein targets via shape-specific recognition (analogous to antibody-antigen binding). As therapeutic agents, the G-rich aptamers may have some advantages over monoclonal antibodies and other oligonucleotide-based approaches. For example, quadruplex oligonucleotides are non-immunogenic, heat stable and they have increased resistance to serum nucleases and enhanced cellular uptake compared to unstructured sequences. In this review, we describe the characteristics and activities of G-rich oligonucleotides. We also give a personal perspective on the discovery and development of AS1411, an antiproliferative G-rich phosphodiester oligonucleotide that is currently being tested as an anticancer agent in Phase II clinical trials. This molecule functions as an aptamer to nucleolin, a multifunctional protein that is highly expressed by cancer cells, both intracellularly and on the cell surface. Thus, the serendipitous discovery of the G-rich oligonucleotides also led to the identification of nucleolin as a new molecular target for cancer therapy.

Indexed as

AnimalsAntineoplastic AgentsAptamers, NucleotideCell ProliferationClinical Trials as TopicDrug DiscoveryDrug Screening Assays, AntitumorHumansMolecular StructureNeoplasmsNucleolinOligodeoxyribonucleotidesPhosphoproteinsRNA-Binding ProteinsAGRO 100Antineoplastic AgentsAptamers, NucleotideNucleolinOligodeoxyribonucleotidesPhosphoproteinsRNA-Binding Proteins

Identifiers

PMID19454272
PMCPMC2716701
OpenAlexW2041919391

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.