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Ultrasound-mediated microbubbles cavitation enhanced chemotherapy of advanced prostate cancer by increasing the permeability of blood-prostate barrier

Authors :
Xuehua Zhu
Zenan Liu
Jianling Yang
Wei He
Tong Liu
Jie Jiang
Xiaofei Hou
Decao Yang
Huile Gao
Haizhui Xia
Jian Lu
Shi Tan
Ye Yan
Ling Ni
Source :
Translational Oncology, Vol 14, Iss 10, Pp 101177-(2021), Translational Oncology
Publication Year :
2021
Publisher :
Elsevier BV, 2021.

Abstract

Highlights • Combination therapy increased cell apoptosis and the inhibition of cell viability. • Combination therapy enhanced chemotherapy efficacy by increasing cell permeability. • Success in developing an orthotopic model of prostate tumor implantation in mice. • Combination therapy inhibited tumor growth and prolonged the survival of mice.<br />Although chemotherapy is an important treatment for advanced prostate cancer, its efficacy is relatively limited. Ultrasound-induced cavitation plays an important role in drug delivery and gene transfection. However, whether cavitation can improve the efficacy of chemotherapy for prostate cancer remains unclear. In this study, we treated RM-1 mouse prostate carcinoma cells with a combination of ultrasound-mediated microbubble cavitation and paclitaxel. Our results showed that combination therapy led to a more pronounced inhibition of cell viability and increased cell apoptosis. The enhanced efficacy of chemotherapy was attributed to the increased cell permeability induced by cavitation. Importantly, compared with chemotherapy alone (nab-paclitaxel), chemotherapy combined with ultrasound-mediated microbubble cavitation significantly inhibited tumor growth and prolonged the survival of tumor-bearing mice in an orthotopic mouse model of RM-1 prostate carcinoma, indicating the synergistic effects of combined therapy on tumor reduction. Furthermore, we analyzed tumor-infiltrating lymphocytes and found that during chemotherapy, the proportions of CTLA4+ cells and PD-1+/CTLA4+ cells in CD8+ T cells slightly increased after cavitation treatment.

Details

ISSN :
19365233
Volume :
14
Database :
OpenAIRE
Journal :
Translational Oncology
Accession number :
edsair.doi.dedup.....b97b8e367ea667d17335f493ecd1e32e
Full Text :
https://doi.org/10.1016/j.tranon.2021.101177