Evidence map›Paper›PMID 28615299›Full record

ArticleMolecular cancer therapeutics2017

Ormeloxifene Suppresses Prostate Tumor Growth and Metastatic Phenotypes via Inhibition of Oncogenic β-catenin Signaling and EMT Progression.

Bilal Bin Hafeez, Aditya Ganju, Mohammed Sikander, Vivek K Kashyap, Zubair Bin Hafeez, Neeraj Chauhan, Shabnam Malik, Andrew E Massey, Manish K Tripathi, Fathi T Halaweish and 5 more

Abstract read
In one paragraph

Article in Molecular cancer therapeutics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

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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

15 authors.

Bilal Bin HafeezDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Centre, Memphis, Tennessee.
Aditya GanjuDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Centre, Memphis, Tennessee.
Mohammed SikanderDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Centre, Memphis, Tennessee.
Vivek K KashyapDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Centre, Memphis, Tennessee.
Zubair Bin HafeezDepartment of Biosciences, Jamia Millia Islamia, New Delhi, Delhi, India.
Neeraj ChauhanDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Centre, Memphis, Tennessee.
Shabnam MalikDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Centre, Memphis, Tennessee.
Andrew E MasseyDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Centre, Memphis, Tennessee.
Manish K TripathiDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Centre, Memphis, Tennessee.
Fathi T HalaweishSouth Dakota State University, Brookings, South Dakota.
Nadeem ZafarDepartment of Pathology, University of Tennessee Health Science Center, Memphis, Tennessee.
Man M SinghSaraswati Dental College, Lucknow, Uttar Pradesh, India.
Murali M YallapuDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Centre, Memphis, Tennessee.
Subhash C ChauhanDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Centre, Memphis, Tennessee. schauha1@uthsc.edu mjaggi@uthsc.edu.
Meena JaggiDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Centre, Memphis, Tennessee. schauha1@uthsc.edu mjaggi@uthsc.edu.

Funding

MUC13 Mucin in Colorectal Cancer Health DisparityR01CA204552 · NCI · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI CHAUHAN, SUBHASH C. · 2016 to 2020
$1.7M
Development of Targeted Nanotechnology Platform for Pancreatic CancerR01CA206069 · NCI · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI CHAUHAN, SUBHASH C. · 2016 to 2021
$1.7M
Targeted Nanotherapy for Pancreatic CancerR01CA210192 · NCI · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI CHAUHAN, SUBHASH C. · 2016 to 2021
$1.7M
Etiology of cervical cancer health disparity in American Indian womenU01CA162106 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI CHAUHAN, SUBHASH C., JAGGI, MEENA · 2012 to 2016
$1.5M
Aspects of MUC13 Mucin in CancerR01CA142736 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI CHAUHAN, SUBHASH C. · 2010 to 2013
$1.2M
NCI NIH HHS R01 CA142736NCI NIH HHS R01 CA204552NCI NIH HHS R01 CA206069NCI NIH HHS R01 CA210192NCI NIH HHS U01 CA162106
6 · The paper itself

Abstract

Ormeloxifene is a clinically approved selective estrogen receptor modulator, which has also shown excellent anticancer activity, thus it can be an ideal repurposing pharmacophore. Herein, we report therapeutic effects of ormeloxifene on prostate cancer and elucidate a novel molecular mechanism of its anticancer activity. Ormeloxifene treatment inhibited epithelial-to-mesenchymal transition (EMT) process as evident by repression of N-cadherin, Slug, Snail, vimentin, MMPs (MMP2 and MMP3), β-catenin/TCF-4 transcriptional activity, and induced the expression of pGSK3β. In molecular docking analysis, ormeloxifene showed proficient docking with β-catenin and GSK3β. In addition, ormeloxifene induced apoptosis, inhibited growth and metastatic potential of prostate cancer cells and arrested cell cycle in G

Indexed as

AnimalsApoptosisBenzopyransbeta CateninCell Line, TumorCell ProliferationEpithelial-Mesenchymal TransitionHumansMaleMiceMolecular Docking SimulationNeoplasm MetastasisProstatic NeoplasmsSignal TransductionXenograft Model Antitumor AssaysBenzopyransbeta CateninCTNNB1 protein, humanormeloxifene

Identifiers

PMID28615299
PMCPMC5774234

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Registered trials

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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.