Evidence map›Paper›PMID 19387797›Full record

ArticleMolecular and cellular biochemistry2009

Clinical-translational strategies for the elevation of Nm23-H1 metastasis suppressor gene expression.

Jean-Claude Marshall, Jong Heun Lee, Patricia S Steeg

Abstract read
In one paragraph

Article in Molecular and cellular biochemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Review
  2. Evening Primrose (Antioxidants (Basel, Switzerland) · 2018
    Review
  3. Article
  4. Article
  5. Regulation of the metastasis suppressor Nm23-H1 by tumor viruses.Naunyn-Schmiedeberg's archives of pharmacology · 2015
    Review
  6. Metastasis suppressor genes.Histology and histopathology · 2013
    Review
  7. Genomics screens for metastasis genes.Cancer metastasis reviews · 2012
    Review
  8. Article
  9. Article
  10. Rethinking the metastatic cascade as a therapeutic target.Nature reviews. Clinical oncology · 2011
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. 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

3 authors.

Jean-Claude MarshallWomen's Cancers Section, Laboratory of Molecular Pharmacology, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA. marshallje@mail.nih.gov
Jong Heun Lee
Patricia S Steeg

Funding

Molecular Biology of the Metastatic PhenotypeZIASC000892 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI STEEG, PATRICIA SCHRIVER · 2009 to 2023
$8.4M
MOLECULAR BIOLOGY OF THE METASTATIC PHENOTYPEZ01SC000892 · SC · DIVISION OF CLINICAL SCIENCES - NCI · PI STEEG, PATRICIA SCHRIVER · 1996 to 2008
$1.3M
Intramural NIH HHS Z01 SC000892
6 · The paper itself

Abstract

Interruption of the tumor metastatic process is a new, thought provoking molecular target for the treatment of cancer. The Nm23-H1 metastasis suppressor gene stands as a validated molecular target owing to its reduced expression in many aggressive human tumors, and the reduction in metastatic potential in vivo upon re-expression in multiple cell lines. Several compounds have been identified which elevate Nm23-H1 expression in vitro including indomethacin, gamma Linolenic Acid, trichostatin A, 5-aza-deoxycytidine, and high dose medroxyprogesterone acetate. Using a model of lung metastatic colonization by MDA-MB-231 human breast carcinoma cells, we demonstrated that high dose MPA reduced the formation of overt lung metastases by 37-46% and those metastases that formed were statistically smaller. A Phase II clinical trial of high dose MPA, alone or in combination with metronomic chemotherapy has recently opened.

Indexed as

AnimalsAntineoplastic Agents, HormonalBreast NeoplasmsCell Line, TumorClinical Trials as TopicDisease-Free SurvivalDose-Response Relationship, DrugFemaleFollow-Up StudiesGene Expression Regulation, NeoplasticGenes, Tumor SuppressorHumansMedroxyprogesterone AcetateMiceNM23 Nucleoside Diphosphate KinasesReceptors, GlucocorticoidAntineoplastic Agents, HormonalMedroxyprogesterone AcetateNM23 Nucleoside Diphosphate KinasesReceptors, Glucocorticoid

Identifiers

PMID19387797
PMCPMC3501675

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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.