TY - JOUR
T1 - A Carbon-Caged Rhodamine Generating Nitrosoperoxycarbonate for Photoimmunotherapy
AU - Yin, Lei
AU - Zhao, Bei
AU - Zhou, Jie
AU - Huang, Yunxia
AU - Ma, Hao
AU - Zhou, Ting
AU - Mou, Jie
AU - Min, Peiru
AU - Chen, Jinquan
AU - Ge, Guangbo
AU - Qian, Xuhong
AU - Luo, Xiao
AU - Yang, Youjun
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2024/6/21
Y1 - 2024/6/21
N2 - Photoimmunotherapy is a promising cancer treatment modality. While potent 1-e− oxidative species are known to induce immunogenic cell death (ICD), they are also associated with unspecific oxidation and collateral tissue damage. This difficulty may be addressed by post-generation radical reinforcement. Namely, non-oxidative radicals are first generated and subsequently activated into powerful oxidative radicals to induce ICD. Here, we developed a photo-triggered molecular donor (NPCD565) of nitrosoperoxycarbonate (ONOOCO2−), the first of its class to our knowledge, and further evaluated its feasibility for immunotherapy. Upon irradiation of NPCD565 by light within a broad spectral region from ultraviolet to red, ONOOCO2− is released along with a bright rhodamine dye (RD565), whose fluorescence is a reliable and convenient build-in reporter for the localization, kinetics, and dose of ONOOCO2− generation. Upon photolysis of NPCD565 in 4T1 cells, damage-associated molecular patterns (DAMPs) indicative of ICD were observed and confirmed to exhibit immunogenicity by induced maturation of dendritic cells. In vivo studies with a bilateral tumor-bearing mouse model showcased the potent tumor-killing capability of NPCD565 of the primary tumors and growth suppression of the distant tumors. This work unveils the potent immunogenicity of ONOOCO2−, and its donor (NPCD565) has broad potential for photo-immunotherapy of cancer.
AB - Photoimmunotherapy is a promising cancer treatment modality. While potent 1-e− oxidative species are known to induce immunogenic cell death (ICD), they are also associated with unspecific oxidation and collateral tissue damage. This difficulty may be addressed by post-generation radical reinforcement. Namely, non-oxidative radicals are first generated and subsequently activated into powerful oxidative radicals to induce ICD. Here, we developed a photo-triggered molecular donor (NPCD565) of nitrosoperoxycarbonate (ONOOCO2−), the first of its class to our knowledge, and further evaluated its feasibility for immunotherapy. Upon irradiation of NPCD565 by light within a broad spectral region from ultraviolet to red, ONOOCO2− is released along with a bright rhodamine dye (RD565), whose fluorescence is a reliable and convenient build-in reporter for the localization, kinetics, and dose of ONOOCO2− generation. Upon photolysis of NPCD565 in 4T1 cells, damage-associated molecular patterns (DAMPs) indicative of ICD were observed and confirmed to exhibit immunogenicity by induced maturation of dendritic cells. In vivo studies with a bilateral tumor-bearing mouse model showcased the potent tumor-killing capability of NPCD565 of the primary tumors and growth suppression of the distant tumors. This work unveils the potent immunogenicity of ONOOCO2−, and its donor (NPCD565) has broad potential for photo-immunotherapy of cancer.
KW - Fluorescence-calibration
KW - Immunogenic Cancer Therapy
KW - Nitrosoperoxycarbonate
KW - Photo-trigger
UR - https://www.scopus.com/pages/publications/85194190881
U2 - 10.1002/anie.202402949
DO - 10.1002/anie.202402949
M3 - 文章
C2 - 38644342
AN - SCOPUS:85194190881
SN - 1433-7851
VL - 63
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 26
M1 - e202402949
ER -