Evidence map›Paper›PMID 24389365›Full record

ArticleBone2014

Parathyroid hormone receptor mediates the anti-myeloma effect of proteasome inhibitors.

Maurizio Zangari, Tamara Berno, Ye Yang, Ming Zeng, Hongwei Xu, Lisa Pappas, Guido Tricot, Archana Kamalakar, Donghoon Yoon, Larry J Suva

Abstract read
In one paragraph

Article in Bone, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

10 authors at 4 institutions in 2 countries.

Maurizio ZangariUniversity of Utah, Myeloma Program, Salt Lake City, UT, USA. Electronic address: mzangari2@uams.edu.
Tamara BernoUniversity of Padua, Italy. Electronic address: tamara.berno@unipd.it.
Ye YangUniversity of Utah, Myeloma Program, Salt Lake City, UT, USA. Electronic address: ye.yang@hsc.utah.edu.
Ming ZengUniversity of Utah, Myeloma Program, Salt Lake City, UT, USA. Electronic address: ming.zeng@hsc.utah.edu.
Hongwei XuUniversity of Utah, Myeloma Program, Salt Lake City, UT, USA. Electronic address: hongwei.xu@hsc.utah.edu.
Lisa PappasHuntsman Cancer Institute, Salt Lake City, UT, USA. Electronic address: lisa.pappas@hci.utah.edu.
Guido TricotUniversity of Utah, Myeloma Program, Salt Lake City, UT, USA. Electronic address: guido.tricot@hsc.utah.edu.
Archana KamalakarDepartment of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, AR, USA. Electronic address: akamalakar@uams.edu.
Donghoon YoonMyeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR, USA. Electronic address: DYoon@uams.edu.
Larry J SuvaDepartment of Orthopaedic Surgery, Center for Orthopaedic Research, University of Arkansas for Medical Sciences, Little Rock, AR, USA. Electronic address: suvalarryj@uams.edu.
University of Utah · USUniversity of Arkansas for Medical Sciences · USHuntsman Cancer Institute · USUniversity of Padua · IT

Funding

Breast Cancer Bone MetastasisR01CA166060 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI SUVA, LARRY J. · 2013 to 2017
$1.5M
NCI NIH HHS R01 CA166060NCI NIH HHS R01 CA166060-01A1
6 · The paper itself

Abstract

Clinically significant serum parathyroid hormone (PTH) variations have been reported in multiple myeloma (MM) patients treated with proteasome inhibitors. To elucidate the association between serum PTH variations and proteasome inhibition in MM, the effect of PTH and PTHR1 ligands on the proteasome inhibitors bortezomib and carfilzomib in vitro and in vivo was determined. The MM cell lines ARP1, OC1 and 5TGM1 expressed mRNA and protein encoding PTH receptor 1 (PTHR1). Treatment of 5TGM1 cells with either PTH(1-34), bortezomib or carfilzomib alone dose-dependently inhibited 5TGM1 cell proliferation. However, treatment with the potent PTHR1 antagonist [TYR34]PTH(7-34) (PTH(7-34)) had no significant effect on myeloma cell proliferation and cell viability. In contrast, when used in combination with bortezomib or carfilzomib, PTH(7-34) treatment significantly reduced the bortezomib or carfilzomib-associated decrease in cell proliferation. Treatment of the C57BL/KaLwRij mouse myeloma model with either bortezomib or carfilzomib provided a significantly prolonged survival benefit compared to controls (p=0.04; p=0.01 respectfully). This potent anti-myeloma effect was completely abrogated by concomitant treatment with PTH(7-34). These results suggest an important role of the PTHR1 in the anti-myeloma effect of proteosome inhibition.

Indexed as

AnimalsBoronic AcidsBortezomibCell Line, TumorCell ProliferationDisease Models, AnimalFemaleHumansMaleMiceMultiple MyelomaOligopeptidesProteasome InhibitorsPyrazinesReceptor, Parathyroid Hormone, Type 1Boronic AcidsBortezomibcarfilzomibOligopeptidesProteasome InhibitorsPyrazinesReceptor, Parathyroid Hormone, Type 1Multiple myelomaProteasome inhibitionPTH receptor

Identifiers

PMID24389365
PMCPMC3967551
OpenAlexW2074360971

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.