Could Photodynamic Therapy Be a Promising Therapeutic Modality in Hepatocellular Carcinoma Patients? A Critical Review of Experimental and Clinical Studies.

active targeting anti-cancer therapy anti-tumor immunity cirrhosis passive targeting

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
15 Oct 2021
Historique:
received: 07 06 2021
revised: 22 09 2021
accepted: 02 10 2021
entrez: 23 10 2021
pubmed: 24 10 2021
medline: 24 10 2021
Statut: epublish

Résumé

Photodynamic Therapy (PDT) relies on local or systemic administration of a light-sensitive dye, called photosensitizer, to accumulate into the target site followed by excitation with light of appropriate wavelength and fluence. This photo-activated molecule reacts with the intracellular oxygen to induce selective cytotoxicity of targeted cells by the generation of reactive oxygen species. Hepatocellular carcinoma (HCC), one of the leading causes of cancer-associated mortality worldwide, has insufficient treatment options available. In this review, we discuss the mechanism and merits of PDT along with its recent developments as an anti-cancerous therapy. We also highlight the application of this novel therapy for diagnosis, visualization, and treatment of HCC. We examine the underlying challenges, some pre-clinical and clinical studies, and possibilities of future studies associated with PDT. Finally, we discuss the mechanism of an active immune response by PDT and thereafter explored the role of PDT in the generation of anti-tumor immune response in the context of HCC, with an emphasis on checkpoint inhibitor-based immunotherapy. The objective of this review is to propose PDT as a plausible adjuvant to existing therapies for HCC, highlighting a feasible combinatorial approach for HCC treatment.

Identifiants

pubmed: 34680325
pii: cancers13205176
doi: 10.3390/cancers13205176
pmc: PMC8534013
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

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Auteurs

Abhishek Kumar (A)

INSERM, CHU-Lille, U1189-ONCO-THAI-Assisted Laser Therapy and Immunotherapy for Oncology, University of Lille, F-59000 Lille, France.

Olivier Moralès (O)

INSERM, CHU-Lille, U1189-ONCO-THAI-Assisted Laser Therapy and Immunotherapy for Oncology, University of Lille, F-59000 Lille, France.
CNRS UMS 3702, Lille Institute of Biology, F-59021 Lille, France.

Serge Mordon (S)

INSERM, CHU-Lille, U1189-ONCO-THAI-Assisted Laser Therapy and Immunotherapy for Oncology, University of Lille, F-59000 Lille, France.
INSERM U1026 Bioingénierie Tissulaire (BioTis), Université de Bordeaux, F-33076 Bordeaux, France.

Nadira Delhem (N)

INSERM, CHU-Lille, U1189-ONCO-THAI-Assisted Laser Therapy and Immunotherapy for Oncology, University of Lille, F-59000 Lille, France.

Emmanuel Boleslawski (E)

INSERM, CHU-Lille, U1189-ONCO-THAI-Assisted Laser Therapy and Immunotherapy for Oncology, University of Lille, F-59000 Lille, France.
Department of Digestive Surgery and Liver Transplantation, Hôpital Huriez, Nord-de-France University Hospital, CHU Lille, Service de Chirurgie Digestive et Transplantation, F-59000 Lille, France.

Classifications MeSH