Evidence map›Paper›PMID 37444643›Full record

ArticleCancers2023

Divergent Oxidative Stress in Normal Tissues and Inflammatory Cells in Hodgkin and Non-Hodgkin Lymphoma.

Cecilia Marini, Vanessa Cossu, Francesco Lanfranchi, Sonia Carta, Francesca Vitale, Francesca D'Amico, Matteo Bauckneht, Silvia Morbelli, Maria Isabella Donegani, Silvia Chiola and 12 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. 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
0.7field-weighted citation impact, top 28% 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, 3 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. 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

22 authors at 3 institutions in 1 country.

Cecilia MariniInstitute of Molecular Bioimaging and Physiology (IBFM), National Research Council (CNR), 20054 Milan, Italy.
Vanessa CossuHuman Anatomy Section, Department of Experimental Medicine, University of Genoa, 16132 Genova, Italy.
Francesco LanfranchiDepartment of Health Sciences, University of Genoa, 16132 Genova, Italy.ORCID 0000-0002-6043-9627
Sonia CartaIRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy.ORCID 0000-0002-1278-9761
Francesca VitaleIRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy.
Francesca D'AmicoDepartment of Health Sciences, University of Genoa, 16132 Genova, Italy.ORCID 0000-0002-1859-8958
Matteo BaucknehtIRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy.ORCID 0000-0002-1937-9116
Silvia MorbelliIRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy.
Maria Isabella DoneganiIRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy.
Silvia ChiolaIRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy.
Stefano RaffaIRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy.
Luca SofiaDepartment of Health Sciences, University of Genoa, 16132 Genova, Italy.
Tania Di RaimondoDepartment of Health Sciences, University of Genoa, 16132 Genova, Italy.
Filippo BalleriniIRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy.
Chiara GhiggiIRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy.
Paolo DurandoDepartment of Health Sciences, University of Genoa, 16132 Genova, Italy.ORCID 0000-0001-5047-5176
Silvia RaveraHuman Anatomy Section, Department of Experimental Medicine, University of Genoa, 16132 Genova, Italy.ORCID 0000-0002-0803-1042
Mattia RiondatoIRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy.
Anna Maria OrengoIRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy.
Silvia BrunoHuman Anatomy Section, Department of Experimental Medicine, University of Genoa, 16132 Genova, Italy.
Sabrina ChiesaIRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy.
Gianmario SambucetiIRCCS Ospedale Policlinico San Martino, 16132 Genova, Italy.ORCID 0000-0003-2979-6500
Ospedale Policlinico San Martino · ITUniversity of Genoa · ITInstitute of Molecular Bioimaging and Physiology · IT

Funding

Italian Association for Cancer Research IG 23201
6 · The paper itself

Abstract

backgroundPrevious studies reported mitochondrial and endoplasmic reticulum redox stress in peripheral blood mononucleated cells (PBMCs) of treatment-naïve Hodgkin lymphoma (HL) patients. Here, we assessed whether this response also applies to non-HL (NHL) patients, and whether the oxidative damage is a selective feature of PBMCs or, rather, also affects tissues not directly involved in the inflammatory response.

methodsIsolated PBMCs of 28 HL, 9 diffuse large B cell lymphoma, 8 less aggressive-NHL, and 45 controls underwent flow cytometry to evaluate redox stress and uptake of the glucose analogue 2-NBDG. This analysis was complemented with the assay of malondialdehyde (MDA) levels and enzymatic activity of glucose-6P-dehydrogenase and hexose-6P-dehydrogenase (H6PD). In all lymphoma patients,

resultsMitochondrial reactive oxygen species generation and MDA levels were increased only in HL patients as well as H6PD activity and 2-NBDG uptake. Similarly, myocardial FDG retention was higher in HL than in other groups as opposed to a similar tracer uptake in the skeletal muscle.

conclusionsRedox stress of PBMCs is more pronounced in HL with respect to both NHL groups. This phenomenon is coherent with an increased activity of H6PD that also extends to the myocardium.

Indexed as

2-NBDGendoplasmic reticulumFDG-PET/CTlymphomamitochondriapentose phosphate pathwayredox stress

Identifiers

PMID37444643
PMCPMC10341255
OpenAlexW4383722934

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.