Evidence map›Paper›PMID 20453882›Full record

ArticleOncogene2010

Mechanism of inhibition of MMTV-neu and MMTV-wnt1 induced mammary oncogenesis by RARalpha agonist AM580.

Y Lu, S Bertran, T-A Samuels, R Mira-y-Lopez, E F Farias

Abstract read
In one paragraph

Article in Oncogene, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Vitamin A deficiency attenuates cardiac rupture inFrontiers in cardiovascular medicine · 2025
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  3. A PERK-Specific Inhibitor Blocks Metastatic Progression by Limiting Integrated Stress Response-Dependent Survival of Quiescent Cancer Cells.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  4. Article
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  6. Antagonizing RARγ Drives Necroptosis of Cancer Stem Cells.International journal of molecular sciences · 2022
    Review
  7. Article
  8. Article
  9. Review
  10. Effect of Specific Retinoic Acid Receptor Agonists on Noise-Induced Hearing Loss.International journal of environmental research and public health · 2019
    Article
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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 1 institution in 1 country.

Y LuDivision of Hematology-Oncology, Department of Medicine, Tisch Cancer Center, Mount Sinai School of Medicine, New York, NY, USA.
S Bertran
T-A Samuels
R Mira-y-Lopez
E F Farias
Icahn School of Medicine at Mount Sinai · US

Funding

Advanced Microscopy Shared Resource FacilityR24CA095823 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI FRIEDRICH, VICTOR LOUIS · 2002 to 2006
$1.3M
Oncogeneses and Retinoid ChemopreventionR01CA119018 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI FARIAS, EDUARDO F · 2006 to 2009
$1.2M
CONFOCAL MICROSCOPE FACILITYS10RR009145 · NCRR · MOUNT SINAI SCHOOL OF MEDICINE OF CUNY · PI MASUR, SANDRA K · 1994 to 1994
–
NCI NIH HHS 5R24-CA095823-04NCI NIH HHS R01 CA119018NCI NIH HHS R01-CA119018NCI NIH HHS R24 CA095823NCRR NIH HHS 1S10-RR0-9145-01
6 · The paper itself

Abstract

We hypothesized that specific activation of a single retinoic acid receptor-alpha (RARalpha), without direct and concurrent activation of RARbeta and gamma, will inhibit mammary tumor oncogenesis in murine models relevant to human cancer. A total of 50 uniparous mouse mammary tumor virus (MMTV)-neu and 50 nuliparous MMTV-wnt1 transgenic mice were treated with RARalpha agonist (retinobenzoic acid, Am580) that was added to the diet for 40 (neu) and 35 weeks (wnt1), respectively. Among the shared antitumor effects was the inhibition of epithelial hyperplasia, a significant increase (P<0.05) in tumor-free survival and a reduction in tumor incidence and in the growth of established tumors. In both models, the mechanisms responsible for these effects involved inhibition of proliferation and survival pathways, and induction of apoptosis. The treatment was more effective in the MMTV-wnt1 model in which Am580 also induced differentiation, in both in vivo and three-dimensional (3D) cultures. In these tumors Am580 inhibited the wnt pathway, measured by loss of nuclear beta-catenin, suggesting partial oncogene dependence of therapy. Am580 treatment increased RARbeta and lowered the level of RARgamma, an isotype whose expression we linked with tumor proliferation. The anticancer effect of RARalpha, together with the newly discovered pro-proliferative role of RARgamma, suggests that specific activation of RARalpha and inhibition of RARgamma might be effective in breast cancer therapy.

Indexed as

AnimalsAntineoplastic AgentsBenzoatesCell Line, TumorCell ProliferationCell Transformation, ViralErb-b2 Receptor Tyrosine KinasesFemaleHumansMammary Neoplasms, ExperimentalMammary Tumor Virus, MouseMiceMice, TransgenicOncogenesReceptors, Retinoic AcidRetinoic Acid Receptor alphaAm 580Antineoplastic AgentsBenzoatesErb-b2 Receptor Tyrosine KinasesRARA protein, humanRara protein, mouseReceptors, Retinoic AcidRetinoic Acid Receptor alphaTetrahydronaphthalenesWnt1 Protein

Identifiers

PMID20453882
PMCPMC2891995
OpenAlexW2075852732

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.