5,10,15,20-Tetrakis(4-sulfonatophenyl)porphyrin Zinc and Chloro-aluminum Phthalocyanine Disulfonate in Photodynamic Therapy of Colorectal Adenocarcinoma In Vitro
Language English Country Greece Media print
Document type Journal Article
PubMed
39348959
DOI
10.21873/anticanres.17263
PII: 44/10/4339
Knihovny.cz E-resources
- Keywords
- Colorectal adenocarcinoma, DNA fragmentation, photodynamic therapy, phthalocyanines, porphyrins, reactive oxygen species,
- MeSH
- Adenocarcinoma * drug therapy metabolism pathology MeSH
- HT29 Cells MeSH
- Photochemotherapy * methods MeSH
- Photosensitizing Agents * pharmacology MeSH
- Indoles * pharmacology MeSH
- Colorectal Neoplasms * drug therapy pathology metabolism MeSH
- Humans MeSH
- Metalloporphyrins * pharmacology MeSH
- Organometallic Compounds * pharmacology MeSH
- DNA Damage drug effects MeSH
- Reactive Oxygen Species * metabolism MeSH
- Cell Survival drug effects MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Photosensitizing Agents * MeSH
- Indoles * MeSH
- Metalloporphyrins * MeSH
- Organometallic Compounds * MeSH
- Reactive Oxygen Species * MeSH
- zinc-tetrakis(p-sulfonatophenyl)porphyrin MeSH Browser
BACKGROUND/AIM: Colorectal cancer (CRC) is one of the most widespread malignancies. One of the alternative therapeutic methods appears to be photodynamic therapy (PDT). MATERIALS AND METHODS: This study investigated the efficiency of 5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrin zinc (ZnTPPS4) and chloro-aluminum phthalocyanine disulfonate (ClAlPcS2) with two commercial photosensitive compounds 5,10,15,20-tetrakis(1-methylpyridinium-4-yl)porphyrin (TMPyP) and tetramethylthionine chloride (methylene blue, MB) in PDT for CRC in vitro. In addition to the study of the photodynamic effect on the viability of the colorectal carcinoma cell line HT29, cellular uptake, ROS production, and DNA damage were investigated. RESULTS: All photosensitizers showed good accumulation within HT29 cells, high efficiency in killing the cells, and a concentration-dependent increase in the production of ROS. CONCLUSION: PDT using ZnTPPS4 and ClAlPcS2 may be effective in the treatment of CRC, achieving a similar photocytotoxic effect at much lower concentrations compared to MB.
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