Evidence map›Paper›PMID 25612941›Full record

ArticleLeukemia research2015

Efficacy of panobinostat and marizomib in acute myeloid leukemia and bortezomib-resistant models.

Fernando F Corrales-Medina, Christa A Manton, Robert Z Orlowski, Joya Chandra

Abstract read
In one paragraph

Article in Leukemia research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Molecularly targeted therapy and immunotherapy in leukemias.Journal of hematology & oncology · 2026
    Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. The role of the proteasome in AML.Blood cancer journal · 2016
    Review
  7. 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

4 authors.

Fernando F Corrales-MedinaDepartment of Pediatrics Research, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Unit 0853, Houston, TX 77030, USA; Division of Pediatric Hematology-Oncology, Department of Pediatrics. University of Miami-Miller School of Medicine, Miami, FL 33136.
Christa A MantonDepartment of Pediatrics Research, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Unit 0853, Houston, TX 77030, USA; The University of Texas Graduate School of Biomedical Sciences at Houston, The University of Texas MD Anderson Cancer Center, 6767 Bertner Avenue, Houston, TX 77030, USA.
Robert Z OrlowskiDepartment of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Unit 0429, Houston, TX 77030, USA.
Joya ChandraDepartment of Pediatrics Research, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Unit 0853, Houston, TX 77030, USA; The University of Texas Graduate School of Biomedical Sciences at Houston, The University of Texas MD Anderson Cancer Center, 6767 Bertner Avenue, Houston, TX 77030, USA. Electronic address: jchandra@mdanderson.org.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
University of Texas M.D. Anderson Cancer SPORE-LeukemiaP50CA100632 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KONOPLEVA, MARINA Y · 2003 to 2023
$43.7M
P4 -TARGETING MULTIPLE MYELOMA BY COMBINING CDK INHIBITORS AND BCL-2 ANTAGONISTSP50CA142509 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KWAK, LARRY W · 2010 to 2014
$11.1M
Role of Redox Dependent Signaling in LeukemiaR01CA115811 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CHANDRA, JOYA · 2007 to 2010
$1.3M
NCI NIH HHS CA100632NCI NIH HHS CA142509NCI NIH HHS P30 CA016672NCI NIH HHS P30CA016672NCI NIH HHS P50 CA100632NCI NIH HHS P50 CA142509NCI NIH HHS R01 CA115811
6 · The paper itself

Abstract

Current relapse rates in acute myeloid leukemia (AML) highlight the need for new therapeutic strategies. Panobinostat, a novel pan-histone deacetylase inhibitor, and marizomib, a second-generation proteasome inhibitor, are emerging as valuable therapeutic options for hematological malignancies. Here we evaluated apoptotic effects of this combinatorial therapy in AML models and report earlier and higher reactive oxygen species induction and caspase-3 activation and greater caspase-8 dependence than with other combinations. In a bortezomib refractory setting, panobinostat induced high levels of DNA fragmentation, and its action was significantly augmented when combined with marizomib. These data support further study of this combination in hematological malignancies.

Indexed as

Antineoplastic AgentsApoptosisBlotting, WesternBoronic AcidsBortezomibCaspasesCell ProliferationDrug CombinationsDrug Resistance, NeoplasmFlow CytometryHumansHydroxamic AcidsIndolesLactonesLeukemia, Myeloid, AcutePanobinostatAntineoplastic AgentsBoronic AcidsBortezomibCaspasesDrug CombinationsHydroxamic AcidsIndolesLactonesmarizomibPanobinostatProteasome InhibitorsPyrazinesPyrrolesAcute myeloid leukemiaBortezomibMarizomibMultiple myelomaPanobinostat

Identifiers

PMID25612941
PMCPMC4420632

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.