Evidence map›Paper›PMID 28494348›Full record

ArticleNeoplasia (New York, N.Y.)2017

Withaferin A Inhibits Prostate Carcinogenesis in a PTEN-deficient Mouse Model of Prostate Cancer.

Jim Moselhy, Suman Suman, Mohammed Alghamdi, Balaji Chandarasekharan, Trinath P Das, Alatassi Houda, Murali Ankem, Chendil Damodaran

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2017. 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
11.0field-weighted citation impact, top 2% 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, 45 citations in OpenAlex.

  1. International journal of molecular sciences · 2025
    Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Novel molecules as the emerging trends in cancer treatment: an update.Medical oncology (Northwood, London, England) · 2022
    Review
  8. A Perspective onJournal of immunology research · 2021
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Journal of traditional and complementary medicine · 2020
    Article
  14. International journal of molecular sciences · 2019
    Review
  15. Article
  16. Article
  17. MicroRNA-21 promotes endometrial carcinoma proliferation and invasion by targeting PTEN.International journal of clinical and experimental pathology · 2017
    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

8 authors at 1 institution in 1 country.

Jim MoselhyDepartment of Urology, University of Louisville, KY, USA.
Suman SumanDepartment of Urology, University of Louisville, KY, USA.
Mohammed AlghamdiDepartment of Pathology, University of Louisville, KY, USA.
Balaji ChandarasekharanDepartment of Urology, University of Louisville, KY, USA.
Trinath P DasDepartment of Urology, University of Louisville, KY, USA.
Alatassi HoudaDepartment of Pathology, University of Louisville, KY, USA.
Murali AnkemDepartment of Urology, University of Louisville, KY, USA.
Chendil DamodaranDepartment of Urology, University of Louisville, KY, USA. Electronic address: chendil.damodaran@louisville.edu.
University of Louisville · US

Funding

Targeting AR and Akt for the Treatment of Prostate CancerR01CA138797 · NCI · UNIVERSITY OF LOUISVILLE · PI DAMODARAN, CHENDIL · 2010 to 2015
$1.5M
Dietary prevention of prostate cancerR01CA140605 · NCI · UNIVERSITY OF LOUISVILLE · PI DAMODARAN, CHENDIL · 2010 to 2015
$1.5M
NCI NIH HHS R01 CA138797NCI NIH HHS R01 CA140605
6 · The paper itself

Abstract

We recently demonstrated that AKT activation plays a role in prostate cancer progression and inhibits the pro-apoptotic function of FOXO3a and Par-4. AKT inhibition and Par-4 induction suppressed prostate cancer progression in preclinical models. Here, we investigate the chemopreventive effect of the phytonutrient Withaferin A (WA) on AKT-driven prostate tumorigenesis in a Pten conditional knockout (Pten-KO) mouse model of prostate cancer. Oral WA treatment was carried out at two different doses (3 and 5 mg/kg) and compared to vehicle over 45 weeks. Oral administration of WA for 45 weeks effectively inhibited primary tumor growth in comparison to vehicle controls. Pathological analysis showed the complete absence of metastatic lesions in organs from WA-treated mice, whereas discrete metastasis to the lungs was observed in control tumors. Immunohistochemical analysis revealed the down-regulation of pAKT expression and epithelial-to-mesenchymal transition markers, such as β-catenin and N-cadherin, in WA-treated tumors in comparison to controls. This result corroborates our previous findings from both cell culture and xenograft models of prostate cancer. Our findings demonstrate that the daily administration of a phytonutrient that targets AKT activation provides a safe and effective treatment for prostate cancer in a mouse model with strong potential for translation to human disease.

Indexed as

AnimalsApoptosisCadherinsCarcinogenesisCell Line, TumorDisease Models, AnimalEpithelial-Mesenchymal TransitionHumansMaleMicePhytochemicalsProstatic NeoplasmsProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseWithanolidesXenograft Model Antitumor AssaysCadherinsPhytochemicalsProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, humanwithaferin AWithanolides

Identifiers

PMID28494348
PMCPMC5421823
OpenAlexW2611951386

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.