Low-intensity ultrasound inhibits melanoma cell proliferation in vitro and tumor growth in vivo

被引:3
|
作者
Feril, Loreto B., Jr. [1 ]
Yamaguchi, Kazuki [1 ,2 ]
Ikeda-Dantsuji, Yurika [3 ]
Furusawa, Yukihiro [4 ]
Tabuchi, Yoshiaki [5 ]
Takasaki, Ichiro [5 ,6 ]
Ogawa, Ryohei [7 ]
Cui, Zheng-Guo [8 ]
Tachibana, Katsuro [1 ]
机构
[1] Fukuoka Univ, Dept Anat, Sch Med, Jonan Ku, 7-45-1 Nanakuma, Fukuoka 8140180, Japan
[2] Fukuoka Univ, Dept Dermatol, Sch Med, Fukuoka 8140180, Japan
[3] Natl Inst Infect Dis, Dept Chemotherapy & Mycosis, Tokyo, Japan
[4] Toyama Prefecture Univ, Dept Liberal Arts & Sci, Toyama 9390398, Japan
[5] Univ Toyama, Life Sci Res Ctr, Div Mol Genet Res, Sugitani, Toyama 9300194, Japan
[6] Univ Toyama, Grad Sch Sci & Engn, Dept Pharmacol, 2630 Sugitani, Toyama 9300194, Japan
[7] Univ Toyama, Grad Sch Med & Pharmaceut Sci, Dept Radiol Sci, 2630 Sugitani, Toyama 9300194, Japan
[8] Univ Fukui, Sch Med Sci, Dept Environm Sci, Fukui 9101193, Japan
关键词
Ultrasound; Cancer; Melanoma; Growth inhibition; Gene regulation; FREE-RADICAL PRODUCTION; PULSED ULTRASOUND; FOCUSED ULTRASOUND; INDUCED APOPTOSIS; FACTOR-ALPHA; CANCER; EXPRESSION; SONOTRANSFECTION; ENHANCEMENT; INVASION;
D O I
10.1007/s10396-021-01131-0
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose To determine the effect of low-intensity ultrasound on cancer cell proliferation in vitro and tumor growth in vivo. Methods In vitro, several cancer cell lines were exposed to low-intensity ultrasound at 0.11 W/cm(2) for 2 min. Of the cell lines screened, melanoma C32 is one of the cell lines that showed sensitivity to growth inhibition by ultrasound and was therefore used in succeeding experiments. In vivo, under the same ultrasound conditions used in vitro, C32 tumors in mice were exposed to ultrasound daily for 2 weeks, and the tumor volumes were monitored weekly using sonography. Results In vitro, C32 cell growth was inhibited, attaining 43.2% inhibition on the 3rd day. In vivo, tumor growth was significantly inhibited, with the treated tumors exhibiting 2.7-fold slowed tumor growth vs. untreated tumors at week 2. Such inhibition was not associated with increased cell death. Several genes related to the cell cycle and proliferation were among those significantly regulated. Conclusion These findings highlight the potential of low-intensity ultrasound to inhibit tumor growth in a noninvasive, safe, and easy-to-administer way. In addition, this may suggest that the mechanical stress induced by ultrasound on C32 cells may have affected the intrinsic biomolecular mechanism related to the cell growth of this particular cell line. Further research is needed to identify which of the regulated genes played key roles in growth inhibition.
引用
收藏
页码:451 / 461
页数:11
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