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Effects of high-intensity focused ultrasound on cisplatin-resistant human lung adenocarcinoma <italic>in vitro</italic> and <italic>in vivo</italic>
Author(s) -
Tao Zhang,
Libin Chen,
Shengmin Zhang,
Youfeng Xu,
Yabo Fan,
Lizhong Zhang
Publication year - 2017
Publication title -
acta biochimica et biophysica sinica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.771
H-Index - 57
eISSN - 1745-7270
pISSN - 1672-9145
DOI - 10.1093/abbs/gmx107
Subject(s) - in vivo , cisplatin , cancer research , a549 cell , apoptosis , cell cycle , in vitro , adenocarcinoma , high intensity focused ultrasound , cell growth , chemistry , microbiology and biotechnology , biology , medicine , cancer , chemotherapy , ultrasound , biochemistry , genetics , radiology
It is widely accepted that high-intensity focused ultrasound (HIFU) is a minimally invasive treatment option for different tumors, but its roles and the corresponding mechanism in cisplatin (DDP) chemoresistance in lung adenocarcinoma (LA) remain unclear. In this study, we investigated the response of DDP-resistant LA cells to HIFU and its underlying molecular mechanisms using molecular biology techniques. It was found that HIFU exposure inhibited the proliferation of DDP-resistant A549 (A549/DDP) cells through arresting cell cycle at the G1/G0 phase via the Cyclin-dependent pathway and promoting apoptosis in a Bcl-2-dependent manner. Furthermore, the results also showed that HIFU exposure could down-regulate the expressions of MDR1, MRP1, and LRP mRNAs, as well as P-gp, MRP1, and LRP proteins related to drug resistance in A549/DDP cells. In vivo experiments also demonstrated that HIFU could reduce the size and mass of subcutaneously transplanted tumors produced by A549/DDP cells through mediating Cyclin-dependent and Bcl-2-dependent pathways. These results suggested that HIFU treatment could inhibit the proliferation of DDP-resistant lung cancer cells and might be a novel therapeutic method for patients with DDP resistance.

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