Cucurbitacin I Suppressed Stem-Like Property and Enhanced Radiation-Induced Apoptosis in Head and Neck Squamous Carcinoma-Derived CD44+ ALDH1+ Cells

被引:107
作者
Chen, Yi-Wei [1 ,6 ]
Chen, Kuan-Hsuan [1 ]
Huang, Pin-I [1 ,6 ]
Chen, Yu-Chih [1 ,5 ]
Chiou, Guang-Yu [1 ,5 ]
Lo, Wen-Liang [2 ,7 ]
Tseng, Ling-Ming [1 ,8 ]
Hsu, Han-Sui [3 ,8 ]
Chang, Kuo-Wei [2 ]
Chiou, Shih-Hwa [1 ,4 ,5 ]
机构
[1] Natl Yang Ming Univ, Inst Clin Med, Taipei 112, Taiwan
[2] Natl Yang Ming Univ, Sch Dent, Dept Dent, Taipei 112, Taiwan
[3] Natl Yang Ming Univ, Inst Emergency & Crit Care Med, Taipei 112, Taiwan
[4] Natl Yang Ming Univ, Inst Pharmacol, Taipei 112, Taiwan
[5] Taipei Vet Gen Hosp, Dept Educ & Res, Taipei, Taiwan
[6] Taipei Vet Gen Hosp, Ctr Canc, Taipei, Taiwan
[7] Taipei Vet Gen Hosp, Div Oral & Maxillofacial Surg, Dept Stomatol, Taipei, Taiwan
[8] Taipei Vet Gen Hosp, Dept Surg, Taipei, Taiwan
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; SIGNAL TRANSDUCER; STAT PROTEINS; CANCER; INHIBITION; GROWTH; TRANSCRIPTION-3; ACTIVATOR; TUMOR; IDENTIFICATION;
D O I
10.1158/1535-7163.MCT-10-0504
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Head and neck squamous cell carcinoma (HNSCC) is a prevalent cancer worldwide. Signal transducers and activators of transcription 3 (STAT3) signaling is reported to promote tumor malignancy and recurrence in HNSCC. Cucurbitacins, triterpenoid derivatives, are strong STAT3 inhibitors with anticancer properties. Recent studies have shown aldehyde dehydrogenase 1 (ALDH1) to be a marker of cancer stem cells (CSC) in HNSCC. The aim of this study was to investigate the therapeutic effect of cucurbitacin I in HNSCC-derived CSCs. Using immunohistochemical analysis, we firstly showed that CD44, ALDH1, and phosphorylated STAT3 (p-STAT3) were higher in high-grade HNSCCs, and that triple positivity for CD44/ALDH1/p-STAT3 indicated a worse prognosis for HNSCC patients. Secondly, CD44(+) ALDH1(+) cells isolated from seven HNSCC patients showed greater tumorigenicity, radioresistance, and high expression of stemness (Bmi-1/Oct-4/Nanog) and epithelial-mesenchymal-transitional (Snail/Twist) genes as p-STAT3 level increased. Furthermore, we found that cucurbitacin I (JSI-124) can effectively inhibit the expression of p-STAT3 and capacities for tumorigenicity, sphere formation, and radioresistance in HNSCC-CD44(+) ALDH1(+). Notably, 150 nmol/L cucurbitacin I effectively blocked STAT3 signaling and downstream survivin and Bcl-2 expression, and it induced apoptosis in HNSCC-CD44(+) ALDH1(+). Moreover, microarray data indicated that 100 nmol/L cucurbitacin I facilitated CD44(+) ALDH1(+) cells to differentiate into CD44(-)ALDH1(-) and enhanced the radiosensitivity of HNSCC-CD44(+) ALDH1(+). Xenotransplant experiments revealed that cucurbitacin I combined with radiotherapy significantly suppressed tumorigenesis and lungmetastasis and further improved the survival rate in HNSCC-CD44(+) ALDH1(+)-transplanted immunocompromised mice. Taken together, our data show that cucurbitacin I, STAT3 inhibitor, reduces radioresistant, distant-metastatic, and CSC-like properties of HNSCC-CD44(+) ALDH1(+) cells. The potential of cucurbitacin I as a radiosensitizer should be verified in future anti-CSC therapy. Mol Cancer Ther; 9(11); 2879-92. (C) 2010 AACR.
引用
收藏
页码:2879 / 2892
页数:14
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