Evidence map›Paper›PMID 38807597›Full record

ArticleFrontiers in immunology2024

Protein kinase CK2α is overexpressed in classical hodgkin lymphoma, regulates key signaling pathways, PD-L1 and may represent a new target for therapy.

Edoardo Ruggeri, Federica Frezzato, Nayla Mouawad, Marco Pizzi, Federico Scarmozzino, Guido Capasso, Valentina Trimarco, Laura Quotti Tubi, Alessandro Cellini, Chiara Adele Cavarretta and 9 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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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

19 authors.

Edoardo RuggeriHematology Unit, Department of Medicine (DIMED), University of Padova, Padova, Italy.
Federica FrezzatoHematology Unit, Department of Medicine (DIMED), University of Padova, Padova, Italy.
Nayla MouawadHematology Unit, Department of Medicine (DIMED), University of Padova, Padova, Italy.
Marco PizziSurgical Pathology and Cytopathology Unit, Department of Medicine, University of Padova, Padova, Italy.
Federico ScarmozzinoSurgical Pathology and Cytopathology Unit, Department of Medicine, University of Padova, Padova, Italy.
Guido CapassoHematology Unit, Department of Medicine (DIMED), University of Padova, Padova, Italy.
Valentina TrimarcoHematology Unit, Department of Medicine (DIMED), University of Padova, Padova, Italy.
Laura Quotti TubiHematology Unit, Department of Medicine (DIMED), University of Padova, Padova, Italy.
Alessandro CelliniHematology Unit, Department of Medicine (DIMED), University of Padova, Padova, Italy.
Chiara Adele CavarrettaHematology Unit, Department of Medicine (DIMED), University of Padova, Padova, Italy.
Valeria RuoccoHematology Unit, Department of Medicine (DIMED), University of Padova, Padova, Italy.
Andrea SerafinHematology Unit, Department of Medicine (DIMED), University of Padova, Padova, Italy.
Francesco AngotziHematology Unit, Department of Medicine (DIMED), University of Padova, Padova, Italy.
Nicolò DanesinHematology Unit, Department of Medicine (DIMED), University of Padova, Padova, Italy.
Sabrina ManniHematology Unit, Department of Medicine (DIMED), University of Padova, Padova, Italy.
Monica FaccoHematology Unit, Department of Medicine (DIMED), University of Padova, Padova, Italy.
Francesco PiazzaHematology Unit, Department of Medicine (DIMED), University of Padova, Padova, Italy.
Livio TrentinHematology Unit, Department of Medicine (DIMED), University of Padova, Padova, Italy.
Andrea VisentinHematology Unit, Department of Medicine (DIMED), University of Padova, Padova, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: In classical Hodgkin lymphoma (cHL), the survival of neoplastic cells is mediated by the activation of NF-κB, JAK/STAT and PI3K/Akt signaling pathways. CK2 is a highly conserved serine/threonine kinase, consisting of two catalytic (α) and two regulatory (β) subunits, which is involved in several cellular processes and both subunits were found overexpressed in solid tumors and hematologic malignancies. Methods and results: Biochemical analyses and Conclusions: Our data point out a pivotal role of CK2 in the survival and the activation of key signaling pathways in cHL. The skewed expression between CK2α and CK2β has never been reported in other lymphomas and might be specific for cHL. The effects of CK2 inhibition on PD-L1 expression and the synergistic combination of CX-4945/silmitasertib with MMAE pinpoints CK2 as a high-impact target for the development of new therapies for cHL.

Indexed as

B7-H1 AntigenCasein Kinase IIHodgkin DiseaseSignal TransductionApoptosisCell Line, TumorGene Expression Regulation, NeoplasticHumansNaphthyridinesPhenazinesPhosphorylationB7-H1 AntigenCasein Kinase IICD274 protein, humanCSNK2A1 protein, humanNaphthyridinesPhenazinessilmitasertibanti-CD30CK2classical hodgkin lymphomaMMAEPD-L1

Identifiers

PMID38807597
PMCPMC11130512

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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.