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Cytotoxic Effects of Combinative ZnPcS(4) Photosensitizer Photodynamic Therapy (PDT) and Cannabidiol (CBD) on a Cervical Cancer Cell Line

The most prevalent type of gynecological malignancy globally is cervical cancer (CC). Complicated by tumor resistance and metastasis, it remains the leading cause of cancer deaths in women in South Africa. Early CC is managed by hysterectomy, chemotherapy, radiation, and more recently, immunotherapy...

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Autores principales: Razlog, Radmila, Kruger, Cherie Ann, Abrahamse, Heidi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10094677/
https://www.ncbi.nlm.nih.gov/pubmed/37047123
http://dx.doi.org/10.3390/ijms24076151
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author Razlog, Radmila
Kruger, Cherie Ann
Abrahamse, Heidi
author_facet Razlog, Radmila
Kruger, Cherie Ann
Abrahamse, Heidi
author_sort Razlog, Radmila
collection PubMed
description The most prevalent type of gynecological malignancy globally is cervical cancer (CC). Complicated by tumor resistance and metastasis, it remains the leading cause of cancer deaths in women in South Africa. Early CC is managed by hysterectomy, chemotherapy, radiation, and more recently, immunotherapy. Although these treatments provide clinical benefits, many patients experience adverse effects and secondary CC spread. To minimize this, novel and innovative treatment methods need to be investigated. Photodynamic therapy (PDT) is an advantageous treatment modality that is non-invasive, with limited side effects. The Cannabis sativa L. plant isolate, cannabidiol (CBD), has anti-cancer effects, which inhibit tumor growth and spread. This study investigated the cytotoxic combinative effect of PDT and CBD on CC HeLa cells. The effects were assessed by exposing in vitro HeLa CC-cultured cells to varying doses of ZnPcS(4) photosensitizer (PS) PDT and CBD, with a fluency of 10 J/cm(2) and 673 nm irradiation. HeLa CC cells, which received the predetermined lowest dose concentrations (ICD(50)) of 0.125 µM ZnPcS(4) PS plus 0.5 µM CBD to yield 50% cytotoxicity post-laser irradiation, reported highly significant and advantageous forms of cell death. Flow cytometry cell death pathway quantitative analysis showed that only 13% of HeLa cells were found to be viable, 7% were in early apoptosis and 64% were in late favorable forms of apoptotic cell death, with a minor 16% of necrosis post-PDT. Findings suggest that this combined treatment approach can possibly induce primary cellular destruction, as well as limit CC metastatic spread, and so warrants further investigation.
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spelling pubmed-100946772023-04-13 Cytotoxic Effects of Combinative ZnPcS(4) Photosensitizer Photodynamic Therapy (PDT) and Cannabidiol (CBD) on a Cervical Cancer Cell Line Razlog, Radmila Kruger, Cherie Ann Abrahamse, Heidi Int J Mol Sci Article The most prevalent type of gynecological malignancy globally is cervical cancer (CC). Complicated by tumor resistance and metastasis, it remains the leading cause of cancer deaths in women in South Africa. Early CC is managed by hysterectomy, chemotherapy, radiation, and more recently, immunotherapy. Although these treatments provide clinical benefits, many patients experience adverse effects and secondary CC spread. To minimize this, novel and innovative treatment methods need to be investigated. Photodynamic therapy (PDT) is an advantageous treatment modality that is non-invasive, with limited side effects. The Cannabis sativa L. plant isolate, cannabidiol (CBD), has anti-cancer effects, which inhibit tumor growth and spread. This study investigated the cytotoxic combinative effect of PDT and CBD on CC HeLa cells. The effects were assessed by exposing in vitro HeLa CC-cultured cells to varying doses of ZnPcS(4) photosensitizer (PS) PDT and CBD, with a fluency of 10 J/cm(2) and 673 nm irradiation. HeLa CC cells, which received the predetermined lowest dose concentrations (ICD(50)) of 0.125 µM ZnPcS(4) PS plus 0.5 µM CBD to yield 50% cytotoxicity post-laser irradiation, reported highly significant and advantageous forms of cell death. Flow cytometry cell death pathway quantitative analysis showed that only 13% of HeLa cells were found to be viable, 7% were in early apoptosis and 64% were in late favorable forms of apoptotic cell death, with a minor 16% of necrosis post-PDT. Findings suggest that this combined treatment approach can possibly induce primary cellular destruction, as well as limit CC metastatic spread, and so warrants further investigation. MDPI 2023-03-24 /pmc/articles/PMC10094677/ /pubmed/37047123 http://dx.doi.org/10.3390/ijms24076151 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Razlog, Radmila
Kruger, Cherie Ann
Abrahamse, Heidi
Cytotoxic Effects of Combinative ZnPcS(4) Photosensitizer Photodynamic Therapy (PDT) and Cannabidiol (CBD) on a Cervical Cancer Cell Line
title Cytotoxic Effects of Combinative ZnPcS(4) Photosensitizer Photodynamic Therapy (PDT) and Cannabidiol (CBD) on a Cervical Cancer Cell Line
title_full Cytotoxic Effects of Combinative ZnPcS(4) Photosensitizer Photodynamic Therapy (PDT) and Cannabidiol (CBD) on a Cervical Cancer Cell Line
title_fullStr Cytotoxic Effects of Combinative ZnPcS(4) Photosensitizer Photodynamic Therapy (PDT) and Cannabidiol (CBD) on a Cervical Cancer Cell Line
title_full_unstemmed Cytotoxic Effects of Combinative ZnPcS(4) Photosensitizer Photodynamic Therapy (PDT) and Cannabidiol (CBD) on a Cervical Cancer Cell Line
title_short Cytotoxic Effects of Combinative ZnPcS(4) Photosensitizer Photodynamic Therapy (PDT) and Cannabidiol (CBD) on a Cervical Cancer Cell Line
title_sort cytotoxic effects of combinative znpcs(4) photosensitizer photodynamic therapy (pdt) and cannabidiol (cbd) on a cervical cancer cell line
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10094677/
https://www.ncbi.nlm.nih.gov/pubmed/37047123
http://dx.doi.org/10.3390/ijms24076151
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