Bypassing Ca 2+ Influx for Antimetastasis Photodynamic Therapy via Robust Nucleus-Targeted Near-Infrared Cyanines

Hypoxia-induced tumor metastasis severely hinders the efficacy of photodynamic therapy (PDT) in cancer treatment. Current strategies predominantly offer palliative suppression of the HIF-1α pathway, emphasizing the urgent need for innovative PDT approaches to prevent metastasis from the outset. Our...

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Veröffentlicht in:Nano letters 2024-12, Vol.24 (49), p.15817
Hauptverfasser: Zhang, Xianghan, Zhang, Huaicong, Dong, Qunyan, Qin, Yuan, Cao, Yutian, Zhu, Haixing, Ma, Zimeng, Li, Zehua, Rao, Zhiping, Ning, Pengbo, Tian, Zuhong, Xia, Yuqiong, Yang, Peng, Wang, Zhongliang
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container_end_page
container_issue 49
container_start_page 15817
container_title Nano letters
container_volume 24
creator Zhang, Xianghan
Zhang, Huaicong
Dong, Qunyan
Qin, Yuan
Cao, Yutian
Zhu, Haixing
Ma, Zimeng
Li, Zehua
Rao, Zhiping
Ning, Pengbo
Tian, Zuhong
Xia, Yuqiong
Yang, Peng
Wang, Zhongliang
description Hypoxia-induced tumor metastasis severely hinders the efficacy of photodynamic therapy (PDT) in cancer treatment. Current strategies predominantly offer palliative suppression of the HIF-1α pathway, emphasizing the urgent need for innovative PDT approaches to prevent metastasis from the outset. Our study revealed that typical PDT triggers an increase in cytoplasmic Ca levels, activating HIF-1α, and that reducing Ca levels can, in turn, mitigate metastasis. Considering cytoplasm's role in Ca storage and regulation, we propose that PDT-induced metastasis can be addressed at its source by precise intracellular localization of photosensitizers (PSs). We developed near-infrared (NIR) cyanine PSs with inherent nucleus targeting capabilities. These PSs effectively inhibit cytoplasmic Ca elevation and reduce HIF-1α activity upon irradiation, achieving remarkable antimetastatic effects in 4T1 tumors. Consequently, our findings highlight the pivotal role of Ca in PDT-induced metastasis and provide a robust approach for circumventing metastasis from the outset using new nucleus-targeting organic PSs.
doi_str_mv 10.1021/acs.nanolett.4c04789
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