Evidence map›Paper›PMID 23856074›Full record

ArticleCancer prevention research (Philadelphia, Pa.)2013

Oral administration of a gemini vitamin D analog, a synthetic triterpenoid and the combination prevents mammary tumorigenesis driven by ErbB2 overexpression.

Jae Young So, Joseph E Wahler, Taesook Yoon, Amanda K Smolarek, Yong Lin, Weichung Joe Shih, Hubert Maehr, Milan Uskokovic, Karen T Liby, Michael B Sporn and 1 more

Abstract read
In one paragraph

Article in Cancer prevention research (Philadelphia, Pa.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Mechanistic Insights into the Anticancer Potential ofPharmaceuticals (Basel, Switzerland) · 2025
    Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Vitamin D and breast cancer: Past and present.The Journal of steroid biochemistry and molecular biology · 2018
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. 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 5 institutions in 2 countries.

Jae Young SoDepartment of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, 164 Frelinghuysen Road, Piscataway, NJ 08854, USA.
Joseph E Wahler
Taesook Yoon
Amanda K Smolarek
Yong Lin
Weichung Joe Shih
Hubert Maehr
Milan Uskokovic
Karen T Liby
Michael B Sporn
Nanjoo Suh
Rutgers Cancer Institute of New JerseyCancer Institute of Florida · USDartmouth College · USEwha Womans University · KRRutgers, The State University of New Jersey · US

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Chang S Chan · 1997 to 2026
$94.5M
Inhibition of breast cancer progression by vitamin D analogs and triterpenoidsR01CA127645 · NCI · RUTGERS, THE STATE UNIV OF N.J. · PI SUH, NANJOO · 2008 to 2012
$1.3M
NCI NIH HHS P30 CA072720NCI NIH HHS R01 CA127645
6 · The paper itself

Abstract

HER2 (or ErbB2), a member of ErbB receptor tyrosine kinases, is overexpressed in approximately 20% of human breast cancer, and the ErbB2 signaling pathway is a critical therapeutic target for ErbB2-overexpressing breast cancer. We investigated the inhibitory effects of the Gemini vitamin D analog BXL0124, the synthetic triterpenoid CDDO-Im and the combination on the tumorigenesis of ErbB2-overexpressing breast cancer. MMTV-ErbB2/neu transgenic mice were treated with BXL0124, CDDO-Im, or the combination from three months of age until the end of the experiment. Formation and growth of MMTV-ErbB2/neu mammary tumors were monitored every week, and all three treatments delayed the development of mammary tumors without significant toxicity. Decreased activation of ErbB2 as well as other ErbB receptors, ErbB1 and ErbB3, in MMTV-ErbB2/neu mammary tumors was shown by all treatments. Protein levels of downstream targets of the ErbB2 signaling pathway, including activated-Erk1/2, activated-Akt, c-Myc, CycD1, and Bcl2, were repressed by all three treatments, with the combination treatment exhibiting the strongest effects. To investigate therapeutic efficacy, the combination of BXL0124 and CDDO-Im was given to MMTV-ErbB2/neu mice after mammary tumors were established between 23 and 30 weeks of age. Short-term treatment with the combination did not show effects on tumor growth nor the ErbB2 signaling pathway. The present study shows BXL0124, CDDO-Im, and the combination as potential agents for prevention, but not treatment, against the tumorigenesis of ErbB2-overexpressing breast cancer.

Indexed as

Administration, OralAnimalsAntineoplastic Combined Chemotherapy ProtocolsBlotting, WesternCalcitriolCell Transformation, NeoplasticErb-b2 Receptor Tyrosine KinasesFemaleHumansImidazolesMammary Neoplasms, AnimalMammary Tumor Virus, MouseMiceMice, TransgenicMicroscopy, FluorescenceOleanolic Acid1,25-dihydroxy-21-(3-hydroxy-3-methyl-4,4,4-tributyl)-23-yne-26,27-hexafluorocholecalciferol1-(2-cyano-3,12-dioxooleana-1,9-dien-28-oyl) imidazoleCalcitriolErb-b2 Receptor Tyrosine KinasesImidazolesOleanolic AcidRNA, Messenger

Identifiers

PMID23856074
PMCPMC3767182
OpenAlexW2102040587

What OpenQuestion holds

Textmetadata
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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.