TY - JOUR
T1 - Three-Pronged Induction of Tumor Calcification Synergistic Calcium Immunotherapy Enables Diagnosis and Cure of Cancer
AU - Bai, Shuang
AU - Xu, Shuqin
AU - Lan, Yulu
AU - Lu, Zhixiang
AU - Liu, Long
AU - Song, Weilun
AU - Wu, Rongqian
AU - Ma, Feng
AU - Chen, Hu
AU - Zeng, Yun
AU - Lv, Yi
AU - Liu, Gang
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2025/2/19
Y1 - 2025/2/19
N2 - Tumor calcification is considered to have the superiority of integrating tumor diagnosis and treatment, and it also has been found to be a predictor of favorable prognosis. However, selecting suitable nanocarriers and therapeutic drugs to maximize the tumor calcification efficiency are key factors for improving calcification-medicated theranostics. This study performs a multi-channel calcification nanoinitiator (CalNI, i.e., BP-Cur-Ca@PKLAK) by loading curcumin (Cur) and depositing Ca2+ on black phosphorus (BP) and combined carrying mitochondria-targeting cytotoxic peptide KLAK to boost a triple-induced tumor calcification. CalNI preferentially accumulates inside tumor mitochondria and induces multilevel calcification promotion by the three combined effects of (i) the degradation of BP into PO43− provides the phosphorus source required for calcification; (ii) burst of calcium ions can directly induce cellular calcium overload; (iii) Cur can inhibit calcium efflux thus further aggravate intracellular calcium stress. Moreover, KLAK exhibited enhanced mitochondrial synergistic toxic effects. Notably, the potential function of CalNI on the regulation of macrophage polarization could completely reverse the immunosuppressive microenvironment, and activate the initiation of T cell-mediated immune response. Therefore, this three-pronged CalNI showed a huge promise to be an alternative to conventional oncology therapy, which presents a more satisfactory therapeutic efficiency than any kind of single induction mode.
AB - Tumor calcification is considered to have the superiority of integrating tumor diagnosis and treatment, and it also has been found to be a predictor of favorable prognosis. However, selecting suitable nanocarriers and therapeutic drugs to maximize the tumor calcification efficiency are key factors for improving calcification-medicated theranostics. This study performs a multi-channel calcification nanoinitiator (CalNI, i.e., BP-Cur-Ca@PKLAK) by loading curcumin (Cur) and depositing Ca2+ on black phosphorus (BP) and combined carrying mitochondria-targeting cytotoxic peptide KLAK to boost a triple-induced tumor calcification. CalNI preferentially accumulates inside tumor mitochondria and induces multilevel calcification promotion by the three combined effects of (i) the degradation of BP into PO43− provides the phosphorus source required for calcification; (ii) burst of calcium ions can directly induce cellular calcium overload; (iii) Cur can inhibit calcium efflux thus further aggravate intracellular calcium stress. Moreover, KLAK exhibited enhanced mitochondrial synergistic toxic effects. Notably, the potential function of CalNI on the regulation of macrophage polarization could completely reverse the immunosuppressive microenvironment, and activate the initiation of T cell-mediated immune response. Therefore, this three-pronged CalNI showed a huge promise to be an alternative to conventional oncology therapy, which presents a more satisfactory therapeutic efficiency than any kind of single induction mode.
KW - calcium stress
KW - macrophage polarization
KW - mitochondrial targeting
KW - tumor calcification
UR - https://www.scopus.com/pages/publications/85205546765
U2 - 10.1002/adfm.202414417
DO - 10.1002/adfm.202414417
M3 - 文章
AN - SCOPUS:85205546765
SN - 1616-301X
VL - 35
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 8
M1 - 2414417
ER -