Modulation of tumor-associated macrophage activity with radiation therapy: a systematic review.


Journal

Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al]
ISSN: 1439-099X
Titre abrégé: Strahlenther Onkol
Pays: Germany
ID NLM: 8603469

Informations de publication

Date de publication:
12 2023
Historique:
received: 01 12 2022
accepted: 23 04 2023
medline: 27 11 2023
pubmed: 22 6 2023
entrez: 22 6 2023
Statut: ppublish

Résumé

Tumor-associated macrophages (TAMs) are the most represented cells of the immune system in the tumor microenvironment (TME). Besides its effects on cancer cells, radiation therapy (RT) can alter TME composition. With this systematic review, we provide a better understanding on how RT can regulate macrophage characterization, namely the M1 antitumor and the M2 protumor polarization, with the aim of describing new effective RT models and exploration of the possibility of integrating radiation with other available therapies. A systematic search in line with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines was carried out in PubMed, Google Scholar, and Scopus. Articles from January 2000 to April 2020 which focus on the role of M1 and M2 macrophages in the response to RT were identified. Of the 304 selected articles, 29 qualitative summary papers were included in our analysis (16 focusing on administration of RT and concomitant systemic molecules, and 13 reporting on RT alone). Based on dose intensity, irradiation was classified into low (low-dose irradiation, LDI; corresponding to less than 1 Gy), moderate (moderate-dose irradiation, MDI; between 1 and 10 Gy), and high (high-dose irradiation, HDI; greater than 10 Gy). While HDI seems to be responsible for induced angiogenesis and accelerated tumor growth through early M2-polarized TAM infiltration, MDI stimulates phagocytosis and local LDI may represent a valid treatment option for possible combination with cancer immunotherapeutic agents. TAMs seem to have an ambivalent role on the efficacy of cancer treatment. Radiation therapy, which exerts its main antitumor activity via cell killing, can in turn interfere with TAM characterization through different modalities. The plasticity of TAMs makes them an attractive target for anticancer therapies and more research should be conducted to explore this potential therapeutic strategy.

Identifiants

pubmed: 37347290
doi: 10.1007/s00066-023-02097-3
pii: 10.1007/s00066-023-02097-3
pmc: PMC10673745
doi:

Types de publication

Systematic Review Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1173-1190

Informations de copyright

© 2023. The Author(s).

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Auteurs

Carlotta Becherini (C)

Radiation Oncology, Azienda Universitaria Ospedaliera Careggi, Università degli Studi di Firenze, Largo Brambila 1, 50134, Florence, Italy.

Andrea Lancia (A)

Radiation Oncology Unit, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.

Beatrice Detti (B)

Radiation Oncology, Azienda Universitaria Ospedaliera Careggi, Università degli Studi di Firenze, Largo Brambila 1, 50134, Florence, Italy. Beatrice.detti@aouc.unifi.it.

Sara Lucidi (S)

Radiation Oncology, Santa Chiara Hospital, Trento, Italy.

Daniele Scartoni (D)

Proton Treatment Center, Azienda Provinciale per i Servizi Sanitari, Trento, Italy.

Gianluca Ingrosso (G)

Radiation Oncology Section, Perugia General Hospital, 06129, Perugia, Italy.

Maria Grazia Carnevale (MG)

Department of Experimental and Clinical Biomedical Sciences Mario Serio, University of Florence, Florence, Italy.

Manuele Roghi (M)

Department of Experimental and Clinical Biomedical Sciences Mario Serio, University of Florence, Florence, Italy.

Niccolò Bertini (N)

Department of Experimental and Clinical Biomedical Sciences Mario Serio, University of Florence, Florence, Italy.

Carolina Orsatti (C)

Department of Experimental and Clinical Biomedical Sciences Mario Serio, University of Florence, Florence, Italy.

Monica Mangoni (M)

Department of Experimental and Clinical Biomedical Sciences Mario Serio, University of Florence, Florence, Italy.

Giulio Francolini (G)

Radiation Oncology, Azienda Universitaria Ospedaliera Careggi, Università degli Studi di Firenze, Largo Brambila 1, 50134, Florence, Italy.

Simona Marani (S)

Radiation Oncology Section, Perugia General Hospital, 06129, Perugia, Italy.

Irene Giacomelli (I)

Proton Treatment Center, Azienda Provinciale per i Servizi Sanitari, Trento, Italy.

Mauro Loi (M)

Radiation Oncology, Azienda Universitaria Ospedaliera Careggi, Università degli Studi di Firenze, Largo Brambila 1, 50134, Florence, Italy.

Stefano Pergolizzi (S)

Radiation Oncology Unit-Department of Biomedical, Dental Science and Morphological and Functional Images, University of Messina, Messina, Italy.

Elisabetta Bonzano (E)

Radiation Oncology Unit, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.

Cynthia Aristei (C)

Radiation Oncology Section, Perugia General Hospital, 06129, Perugia, Italy.

Lorenzo Livi (L)

Radiation Oncology, Azienda Universitaria Ospedaliera Careggi, Università degli Studi di Firenze, Largo Brambila 1, 50134, Florence, Italy.
Department of Experimental and Clinical Biomedical Sciences Mario Serio, University of Florence, Florence, Italy.

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