Evidence map›Paper›PMID 21360650›Full record

ArticlePediatric blood & cancer2011

Initial testing (stage 1) of the polyamine analog PG11047 by the pediatric preclinical testing program.

Malcolm A Smith, John M Maris, Richard Lock, E Anders Kolb, Richard Gorlick, Stephen T Keir, Hernan Carol, Christopher L Morton, C Patrick Reynolds, Min H Kang and 1 more

Abstract read
In one paragraph

Article in Pediatric blood & cancer, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Polyamine synthesis as a target ofThe Journal of biological chemistry · 2018
    Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Development of treatment strategies for advanced neuroblastoma.International journal of clinical oncology · 2012
    Review
  14. 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

11 authors at 9 institutions in 2 countries.

Malcolm A SmithCancer Therapy Evaluation Program, NCI, Bethesda, Maryland 20892, USA. smithm@ctep.nci.nih.gov
John M Maris
Richard Lock
E Anders Kolb
Richard Gorlick
Stephen T Keir
Hernan Carol
Christopher L Morton
C Patrick Reynolds
Min H Kang
Peter J Houghton
Children's Cancer Institute Australia · AUTexas Tech University Health Sciences Center · USCenter for Cancer Research · USChildren's Hospital at Montefiore · USChildren's Hospital of Philadelphia · USCommunity Health Systems - Dupont Hospital · USDuke Medical Center · USNationwide Children's Hospital · USSt. Jude Children's Research Hospital · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
TEMODAR RESISTANCE IN CENTRAL NERVOUS SYSTEMP50CA108786 · NCI · DUKE UNIVERSITY · PI BIGNER, DARELL D · 2004 to 2009
$12.3M
ANTINEOPLASTIC ALKYLGLYCEROLIPIDSR01CA042216 · NCI · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI PIANTADOSI, CLAUDE · 1988 to 1990
–
Intramural NIH HHS Z99 CA999999NCI NIH HHS CA108786NCI NIH HHS CA21765NCI NIH HHS N01 CM042216NCI NIH HHS N01-CM-42216NCI NIH HHS P30 CA021765NCI NIH HHS P50 CA108786
6 · The paper itself

Abstract

backgroundPG11047 is a novel conformationally restricted analog of the natural polyamine, spermine that lowers cellular endogenous polyamine levels and competitively inhibits natural polyamine functions leading to cancer cell growth inhibition. The activity of PG11047 was evaluated against the PPTP's in vitro and in vivo panels. PROCEDURES: PG11047 was evaluated against the PPTP in vitro panel using 96 hr exposure at concentrations ranging from 10 nM to 100 µM. It was tested against the PPTP in vivo panels at a dose of 100 mg/kg administered by the intraperitoneal route weekly for 6 weeks.

resultsIn vitro PG11047 demonstrated a concentration-response pattern consistent with cytostatic activity. The median EC(50) for PG11047 was 71 nM. Cell lines of the Ewing sarcoma panel had a lower median EC(50) value compared to the remaining cell lines in the panel, while cell lines of the neuroblastoma panel had a higher median EC(50) value. In vivo PG11047 induced significant differences in EFS distribution compared to control in 5 of 32 (15.6%) of the evaluable solid tumor xenografts and in 0 of 7 (0%) of the evaluable ALL xenografts. The single case of tumor regression occurred in an ependymoma xenograft.

conclusionsFurther pediatric development of PG11047 will require better defining a target population and identifying combinations for which there is a tumor-selective cytotoxic effect. The regression observed for an ependymoma xenograft and the exquisite sensitivity of some Ewing sarcoma cell lines to the antiproliferative effects of PG11047 provide leads for further preclinical investigations.

Indexed as

AnimalsCell Line, TumorChildDose-Response Relationship, DrugDrug Evaluation, PreclinicalFemaleHumansKaplan-Meier EstimateMiceMice, Inbred BALB CMice, SCIDNeoplasmsSpermineXenograft Model Antitumor AssaysSpermine

Identifiers

PMID21360650
PMCPMC3115432
OpenAlexW2005205470

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.