Evidence map›Paper›PMID 32987735›Full record

ArticleCancers2020

Protein Translation Inhibition is Involved in the Activity of the Pan-PIM Kinase Inhibitor PIM447 in Combination with Pomalidomide-Dexamethasone in Multiple Myeloma.

Teresa Paíno, Lorena González-Méndez, Laura San-Segundo, Luis A Corchete, Susana Hernández-García, Andrea Díaz-Tejedor, Esperanza M Algarín, Pedro Mogollón, Montserrat Martín-Sánchez, Norma C Gutiérrez and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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  8. MYC inhibitors in multiple myeloma.Cancer drug resistance (Alhambra, Calif.) · 2021
    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

13 authors at 2 institutions in 1 country.

Teresa PaínoCentro de Investigación del Cáncer-IBMCC (CSIC-Universidad de Salamanca), Complejo Asistencial Universitario de Salamanca-IBSAL, 37007 Salamanca, Spain.ORCID 0000-0002-0201-3572
Lorena González-MéndezCentro de Investigación del Cáncer-IBMCC (CSIC-Universidad de Salamanca), Complejo Asistencial Universitario de Salamanca-IBSAL, 37007 Salamanca, Spain.
Laura San-SegundoCentro de Investigación del Cáncer-IBMCC (CSIC-Universidad de Salamanca), Complejo Asistencial Universitario de Salamanca-IBSAL, 37007 Salamanca, Spain.ORCID 0000-0003-2391-5935
Luis A CorcheteCentro de Investigación del Cáncer-IBMCC (CSIC-Universidad de Salamanca), Complejo Asistencial Universitario de Salamanca-IBSAL, 37007 Salamanca, Spain.ORCID 0000-0003-4577-8599
Susana Hernández-GarcíaCentro de Investigación del Cáncer-IBMCC (CSIC-Universidad de Salamanca), Complejo Asistencial Universitario de Salamanca-IBSAL, 37007 Salamanca, Spain.
Andrea Díaz-TejedorCentro de Investigación del Cáncer-IBMCC (CSIC-Universidad de Salamanca), Complejo Asistencial Universitario de Salamanca-IBSAL, 37007 Salamanca, Spain.
Esperanza M AlgarínCentro de Investigación del Cáncer-IBMCC (CSIC-Universidad de Salamanca), Complejo Asistencial Universitario de Salamanca-IBSAL, 37007 Salamanca, Spain.
Pedro MogollónCentro de Investigación del Cáncer-IBMCC (CSIC-Universidad de Salamanca), Complejo Asistencial Universitario de Salamanca-IBSAL, 37007 Salamanca, Spain.ORCID 0000-0002-6108-0986
Montserrat Martín-SánchezCentro de Investigación del Cáncer-IBMCC (CSIC-Universidad de Salamanca), Complejo Asistencial Universitario de Salamanca-IBSAL, 37007 Salamanca, Spain.
Norma C GutiérrezCentro de Investigación del Cáncer-IBMCC (CSIC-Universidad de Salamanca), Complejo Asistencial Universitario de Salamanca-IBSAL, 37007 Salamanca, Spain.
María-Victoria MateosCentro de Investigación del Cáncer-IBMCC (CSIC-Universidad de Salamanca), Complejo Asistencial Universitario de Salamanca-IBSAL, 37007 Salamanca, Spain.
Mercedes GarayoaCentro de Investigación del Cáncer-IBMCC (CSIC-Universidad de Salamanca), Complejo Asistencial Universitario de Salamanca-IBSAL, 37007 Salamanca, Spain.ORCID 0000-0003-2194-2841
Enrique M OcioHematology Department, Hospital Universitario Marqués de Valdecilla (IDIVAL). Universidad de Cantabria, 39008 Santander, Spain.ORCID 0000-0002-5765-0085
Universidad de Salamanca · ESUniversidad de Cantabria · ES

Funding

Centro en Red de Medicina Regenerativa y Terapia Celular de Castilla y León N/AFundación Científica Asociación Española Contra el Cáncer GCB120981SANFundación Científica Asociación Española Contra el Cáncer INVES18043PAÍNFundación Ramón Areces FRA16/003Instituto de investigación sanitaria Valdecilla (IDIVAL) N/AInstituto de Salud Carlos III PI15/00067Instituto de Salud Carlos III PI15/02156Instituto de Salud Carlos III PI18/01600Junta de Castilla y León BIO/SA05/14Junta de Castilla y León GRS 862/A/13Sociedad Española de Hematología y Hemoterapia N/AUniversidad de Salamanca FS/22-2015
6 · The paper itself

Abstract

backgroundProviral Insertion site for Moloney murine leukemia virus (PIM) kinases are overexpressed in hematologic malignancies, including multiple myeloma. Previous preclinical data from our group demonstrated the anti-myeloma effect of the pan-PIM kinase inhibitor PIM447.

methodsBased on those data, we evaluate here, by in vitro and in vivo studies, the activity of the triple combination of PIM447 + pomalidomide + dexamethasone (PIM-Pd) in multiple myeloma.

resultsOur results show that the PIM-Pd combination exerts a potent anti-myeloma effect in vitro and in vivo, where it markedly delays tumor growth and prolongs survival of treated mice. Mechanism of action studies performed in vitro and on mice tumor samples suggest that the combination PIM-Pd inhibits protein translation processes through the convergent inhibition of c-Myc and mTORC1, which subsequently disrupts the function of eIF4E. Interestingly the MM pro-survival factor IRF4 is also downregulated after PIM-Pd treatment. As a whole, all these molecular changes would promote cell cycle arrest and deregulation of metabolic pathways, including glycolysis and lipid biosynthesis, leading to inhibition of myeloma cell proliferation.

conclusionsAltogether, our data support the clinical evaluation of the triple combination PIM-Pd for the treatment of patients with multiple myeloma.

Indexed as

drug combinationmultiple myelomapan-PIM kinase inhibitorprotein translation

Identifiers

PMID32987735
PMCPMC7598606
OpenAlexW3089019573

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.