Evidence map›Paper›PMID 39005694›Full record

ArticleAmerican journal of cancer research2024

The inhibitory and transcriptional effects of the epigenetic repurposed drugs hydralazine and valproate in lymphoma cells.

Harold Salamanca-Ortiz, Guadalupe Domínguez-Gomez, Alma Chávez-Blanco, Daniel Ortega-Bernal, José Díaz-Chávez, Aurora González-Fierro, Myrna Candelaria-Hernández, Alfonso Dueñas-González

Abstract read
In one paragraph

Article in American journal of cancer research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Hydralazine potentiates the antiproliferative effect of photodynamic therapy on Candida albicans and Candida parapsilosis in vitro.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2026
    Article
  2. 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

8 authors.

Harold Salamanca-OrtizSubdirection of Basic Research, Instituto Nacional de Cancerología (INCan) Tlalpan, Mexico City 14080, Mexico.
Guadalupe Domínguez-GomezSubdirección de Investigación Clínica, Instituto Nacional de Cancerología (INCan) Tlalpan, Mexico City 14080, Mexico.
Alma Chávez-BlancoSubdirection of Basic Research, Instituto Nacional de Cancerología (INCan) Tlalpan, Mexico City 14080, Mexico.
Daniel Ortega-BernalDepartamento de Ciencias Naturales, Unidad Cuajimalpa, Universidad Autónoma Metropolitana Coyoacan, Mexico City 05348, Mexico.
José Díaz-ChávezSubdirection of Basic Research, Instituto Nacional de Cancerología (INCan) Tlalpan, Mexico City 14080, Mexico.
Aurora González-FierroSubdirection of Basic Research, Instituto Nacional de Cancerología (INCan) Tlalpan, Mexico City 14080, Mexico.
Myrna Candelaria-HernándezSubdirección de Investigación Clínica, Instituto Nacional de Cancerología (INCan) Tlalpan, Mexico City 14080, Mexico.
Alfonso Dueñas-GonzálezSubdirection of Basic Research, Instituto Nacional de Cancerología (INCan) Tlalpan, Mexico City 14080, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lymphoma is a disease that affects countless lives each year. In order to combat this disease, researchers have been exploring the potential of DNMTi and HDACi drugs. These drugs target the cellular processes that contribute to lymphomagenesis and treatment resistance. Our research evaluated the effectiveness of a combination of two such drugs, hydralazine (DNMTi) and valproate (HDACi), in B-cell and T-cell lymphoma cell lines. Here we show that the combination of hydralazine and valproate decreased the viability of cells over time, leading to the arrest of cell-cycle and apoptosis in both B and T-cells. This combination of drugs proved to be synergistic, with each drug showing significant growth inhibition individually. Microarray analyses of HuT 78 and Raji cells showed that the combination of hydralazine and valproate resulted in the up-regulation of 562 and 850 genes, respectively, while down-regulating 152 and 650 genes. Several proapoptotic and cell cycle-related genes were found to be up-regulated. Notably, three and five of the ten most up-regulated genes in HuT 78 and Raji cells, respectively, were related to immune function. In summary, our study suggests that the combination of hydralazine and valproate is an effective treatment option for both B- and T-lymphomas. These findings are highly encouraging, and we urge further clinical evaluation to validate our research and potentially improve lymphoma treatment.

Indexed as

hydralazineNon-Hodgkin lymphomavalproate

Identifiers

PMID39005694
PMCPMC11236763

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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.