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Characteristics of an Impaired PDT Response
Author(s) -
Kessel David,
Cho Won Jin,
Rakowski Joseph,
Kim Harold E.,
Kim HyeongReh C.
Publication year - 2021
Publication title -
photochemistry and photobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.818
H-Index - 131
eISSN - 1751-1097
pISSN - 0031-8655
DOI - 10.1111/php.13397
Subject(s) - apoptosis , photodynamic therapy , photosensitizer , cancer research , programmed cell death , reactive oxygen species , hela , mitochondrion , cell culture , head and neck cancer , cancer , biology , chemistry , medicine , microbiology and biotechnology , biochemistry , genetics , photochemistry , organic chemistry
A concurrent human papilloma virus (HPV) infection potentiates the efficacy of ionizing radiation for treatment of head and neck cancer by promoting apoptosis. Studies in cell culture indicated an opposite effect for photodynamic therapy (PDT) when this leads to mitochondrial and ER photodamage. The explanation for this difference in PDT efficacy remains to be established. While apoptosis was impaired in HPV(‐) cells, such cells can be killed via photodamage directed at the ER: this leads to a nonapoptotic death pathway termed paraptosis. No differences in photosensitizer uptake or reactive oxygen species (ROS) production were observed in HPV(+) vs. HPV(‐) tumors. We now provide evidence that death pathways initiated by ER/mitochondrial photodamage leading to either paraptosis or apoptosis are impaired in an HPV(+) head and neck cell line. These results illustrate the complex determinants of PDT efficacy, a topic that has yet to be fully explored.