New molecular targets in Hodgkin and Reed-Sternberg cells.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2023
Historique:
received: 31 01 2023
accepted: 02 05 2023
medline: 5 6 2023
pubmed: 2 6 2023
entrez: 2 6 2023
Statut: epublish

Résumé

Recent discoveries shed light on molecular mechanisms responsible for classical Hodgkin lymphoma (HL) development and progression, along with features of Hodgkin - Reed and Sternberg cells (HRS). Here, we summarize current knowledge on characteristic molecular alterations in HL, as well as existing targeted therapies and potential novel treatments for this disease. We discuss the importance of cluster of differentiation molecule 30 (CD30) and the programmed cell death-1 protein (PD-1) and ligands (PD-L1/2), and other molecules involved in immune modulation in HL. We highlight emerging evidence indicating that the altered function of SWI/SNF-type chromatin remodeling complexes, PRC2, and other epigenetic modifiers, contribute to variations in chromatin status, which are typical for HL. We postulate that despite of the existence of plentiful molecular data, the understanding of HL development remains incomplete. We therefore propose research directions involving analysis of reverse signaling in the PD-1/PD-L1 mechanism, chromatin remodeling, and epigenetics-related alterations, in order to identify HL features at the molecular level. Such attempts may lead to the identification of new molecular targets, and thus will likely substantially contribute to the future development of more effective targeted therapies.

Identifiants

pubmed: 37266436
doi: 10.3389/fimmu.2023.1155468
pmc: PMC10230546
doi:

Substances chimiques

B7-H1 Antigen 0
Programmed Cell Death 1 Receptor 0

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1155468

Informations de copyright

Copyright © 2023 Sadaf, Ambroziak, Binkowski, Kluebsoongnoen, Paszkiewicz-Kozik, Steciuk, Markowicz, Walewski, Sarnowska, Sarnowski and Konopinski.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Hummaira Sadaf (H)

Department of Experimental Immunotherapy, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Department of Biotechnology, Sardar Bahadur Khan Womens' University, Balochistan, Pakistan.

Maciej Ambroziak (M)

Department of Experimental Immunotherapy, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Robert Binkowski (R)

Institute of Biochemistry and Biophysics Polish Academy of Sciences, Warsaw, Poland.

Jakkapong Kluebsoongnoen (J)

Institute of Biochemistry and Biophysics Polish Academy of Sciences, Warsaw, Poland.

Ewa Paszkiewicz-Kozik (E)

Department of Lymphoid Malignancies, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Jaroslaw Steciuk (J)

Institute of Biochemistry and Biophysics Polish Academy of Sciences, Warsaw, Poland.

Sergiusz Markowicz (S)

Department of Experimental Immunotherapy, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Jan Walewski (J)

Department of Lymphoid Malignancies, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Elzbieta Sarnowska (E)

Department of Experimental Immunotherapy, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Tomasz Jacek Sarnowski (TJ)

Institute of Biochemistry and Biophysics Polish Academy of Sciences, Warsaw, Poland.

Ryszard Konopinski (R)

Department of Experimental Immunotherapy, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

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