Evidence map›Paper›PMID 27657380›Full record

ArticleCancer biology & therapy2016

The histone deacetylase inhibitor romidepsin synergizes with lenalidomide and enhances tumor cell death in T-cell lymphoma cell lines.

Maria Cosenza, Monica Civallero, Stefania Fiorcari, Samantha Pozzi, Luigi Marcheselli, Alessia Bari, Paola Ferri, Stefano Sacchi

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

23 citing papers in PubMed, 35 citations in OpenAlex.

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  12. Valproic Acid Inhibits Peripheral T Cell Lymphoma Cells Behaviors via Restraining PI3K/AKT Pathway.Evidence-based complementary and alternative medicine : eCAM · 2022
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  19. Combination Effect of Notch1 and PI3K/AKT/mTOR Signaling Pathways Inhibitors on T-ALL Cell Lines.International journal of hematology-oncology and stem cell research · 2020
    Article
  20. Recent Update of HDAC Inhibitors in Lymphoma.Frontiers in cell and developmental biology · 2020
    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

8 authors at 1 institution in 1 country.

Maria Cosenzaa Program of Innovative Therapies in Oncology and Haematology, Department of Diagnostic Clinical and Public Health Medicine , University of Modena and Reggio Emilia , Modena , Italy.
Monica Civalleroa Program of Innovative Therapies in Oncology and Haematology, Department of Diagnostic Clinical and Public Health Medicine , University of Modena and Reggio Emilia , Modena , Italy.
Stefania Fiorcarib Department of Medical and Surgical Sciences for Children and Adults , University of Modena and Reggio Emilia , Modena , Italy.
Samantha Pozzia Program of Innovative Therapies in Oncology and Haematology, Department of Diagnostic Clinical and Public Health Medicine , University of Modena and Reggio Emilia , Modena , Italy.
Luigi Marchesellia Program of Innovative Therapies in Oncology and Haematology, Department of Diagnostic Clinical and Public Health Medicine , University of Modena and Reggio Emilia , Modena , Italy.
Alessia Baria Program of Innovative Therapies in Oncology and Haematology, Department of Diagnostic Clinical and Public Health Medicine , University of Modena and Reggio Emilia , Modena , Italy.
Paola Ferric Department of Diagnostic Clinical and Public Health Medicine , University of Modena and Reggio Emilia , Modena , Italy.
Stefano Sacchia Program of Innovative Therapies in Oncology and Haematology, Department of Diagnostic Clinical and Public Health Medicine , University of Modena and Reggio Emilia , Modena , Italy.
University of Modena and Reggio Emilia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We investigated the cytotoxic interactions of romidepsin, a histone deacetylase inhibitor, and lenalidomide, an immunomodulatory agent, in a T-cell lymphoma preclinical model. Hut-78 and Karpas-299 cells were treated with romidepsin and lenalidomide alone and in combination. The interaction between romidepsin and lenalidomide was evaluated by the Chou-Talalay method, and cell viability and clonogenicity were also evaluated. Apoptosis, reactive oxygen species (ROS) levels, and cell cycle distribution were determined by flow cytometry. ER stress, caspase activation, and the AKT, MAPK/ERK, and STAT-3 pathways were analyzed by Western blot. Combination treatment with romidepsin and lenalidomide had a synergistic effect in Hut-78 cells and an additive effect in Karpas-299 cells at 24 hours and did not decrease the viability of normal peripheral blood mononuclear cells. This drug combination induced apoptosis, increased ROS production, and activated caspase-8, -9, -3 and PARP. Apoptosis was associated with increased hallmarks of ER stress and activation of UPR sensors and was mediated by dephosphorylation of the AKT, MAPK/ERK, and STAT3 pathways.The combination of romidepsin and lenalidomide shows promise as a possible treatment for T-cell lymphoma. This work provides a basis for further studies.

Indexed as

Lenalidomideromidepsinsynergistic interactionT-cell lymphomatumor cell death

Identifiers

PMID27657380
PMCPMC5079402
OpenAlexW2514135529

What OpenQuestion holds

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LicenceCC BY-NC
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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.