Evidence map›Paper›PMID 26038698›Full record

ArticlePharmacology research & perspectives2015

Analysis of differential secondary effects of novel rexinoids: select rexinoid X receptor ligands demonstrate differentiated side effect profiles.

Pamela A Marshall, Peter W Jurutka, Carl E Wagner, Arjan van der Vaart, Ichiro Kaneko, Pedro I Chavez, Ning Ma, Jaskaran S Bhogal, Pritika Shahani, Johnathon C Swierski and 1 more

Open access · goldAbstract read
In one paragraph

Article in Pharmacology research & perspectives, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  10. The multi-faceted role of retinoid X receptor in bone remodeling.Cellular and molecular life sciences : CMLS · 2017
    Review
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 3 institutions in 1 country.

Pamela A MarshallSchool of Mathematical and Natural Sciences, New College of Interdisciplinary Arts and Sciences, Arizona State University 4701 W Thunderbird Rd, Glendale, Arizona, 85306.
Peter W JurutkaSchool of Mathematical and Natural Sciences, New College of Interdisciplinary Arts and Sciences, Arizona State University 4701 W Thunderbird Rd, Glendale, Arizona, 85306.
Carl E WagnerSchool of Mathematical and Natural Sciences, New College of Interdisciplinary Arts and Sciences, Arizona State University 4701 W Thunderbird Rd, Glendale, Arizona, 85306.
Arjan van der VaartDepartment of Chemistry, University of South Florida 4202 E Fowler Ave CHE 205, Tampa, Florida, 33620.
Ichiro KanekoSchool of Mathematical and Natural Sciences, New College of Interdisciplinary Arts and Sciences, Arizona State University 4701 W Thunderbird Rd, Glendale, Arizona, 85306.
Pedro I ChavezBiomedical Sciences Program, Midwestern University 19555 N 59th Ave., Glendale, Arizona, 86308.
Ning MaDepartment of Chemistry, University of South Florida 4202 E Fowler Ave CHE 205, Tampa, Florida, 33620.
Jaskaran S BhogalSchool of Mathematical and Natural Sciences, New College of Interdisciplinary Arts and Sciences, Arizona State University 4701 W Thunderbird Rd, Glendale, Arizona, 85306.
Pritika ShahaniSchool of Mathematical and Natural Sciences, New College of Interdisciplinary Arts and Sciences, Arizona State University 4701 W Thunderbird Rd, Glendale, Arizona, 85306.
Johnathon C SwierskiSchool of Mathematical and Natural Sciences, New College of Interdisciplinary Arts and Sciences, Arizona State University 4701 W Thunderbird Rd, Glendale, Arizona, 85306.
Mairi MacNeillSchool of Mathematical and Natural Sciences, New College of Interdisciplinary Arts and Sciences, Arizona State University 4701 W Thunderbird Rd, Glendale, Arizona, 85306.
Arizona State University · USUniversity of South Florida · USMidwestern University · US

Funding

Modeling, Synthesis, and Biological Evaluation of Potential RXT Selective AgonistR15CA139364 · NCI · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI WAGNER, CARL EDWARD · 2011 to 2011
$458k
NCI NIH HHS R15 CA139364
6 · The paper itself

Abstract

In order to determine the feasibility of utilizing novel rexinoids for chemotherapeutics and as potential treatments for neurological conditions, we undertook an assessment of the side effect profile of select rexinoid X receptor (RXR) analogs that we reported previously. We assessed pharmacokinetic profiles, lipid and thyroid-stimulating hormone (TSH) levels in rats, and cell culture activity of rexinoids in sterol regulatory element-binding protein (SREBP) induction and thyroid hormone inhibition assays. We also performed RNA sequencing of the brain tissues of rats that had been dosed with the compounds. We show here for the first time that potent rexinoid activity can be uncoupled from drastic lipid changes and thyroid axis variations, and we propose that rexinoids can be developed with improved side effect profiles than the parent compound, bexarotene (1).

Indexed as

BexarotenelipidsrexinoidsRXRthyroid

Identifiers

PMID26038698
PMCPMC4448986
OpenAlexW2050487907

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.