Honokiol radiosensitizes colorectal cancer cells: enhanced activity in cells with mismatch repair defects

被引:25
作者
He, Zhiyun [4 ,5 ]
Subramaniam, Dharmalingam [1 ]
Ramalingam, Satish [1 ]
Dhar, Animesh [2 ]
Postier, Russell G. [6 ]
Umar, Shahid [5 ]
Zhang, Youcheng [4 ]
Anant, Shrikant [1 ,3 ]
机构
[1] Univ Kansas, Dept Mol & Integrat Physiol, Med Ctr, Kansas City, KS 66160 USA
[2] Univ Kansas, Dept Canc Biol, Med Ctr, Kansas City, KS 66160 USA
[3] Univ Kansas, Ctr Canc, Med Ctr, Kansas City, KS 66160 USA
[4] Lanzhou Univ, Hosp 2, Dept Med, Lanzhou 730000, Gansu, Peoples R China
[5] Univ Oklahoma, Hlth Sci Ctr, Dept Med, Oklahoma City, OK USA
[6] Univ Oklahoma, Hlth Sci Ctr, Dept Surg, Oklahoma City, OK USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2011年 / 301卷 / 05期
基金
美国国家卫生研究院;
关键词
radiation; mismatch repair; cell cycle; p53; apoptosis; MICROSATELLITE-INSTABILITY; COLON-CANCER; TUMOR-CELLS; ADJUVANT CHEMOTHERAPY; IONIZING-RADIATION; CYCLE CHECKPOINT; CARCINOMA; CURCUMIN; PROTEIN; MLH1;
D O I
10.1152/ajpgi.00159.2011
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
He Z, Subramaniam D, Ramalingam S, Dhar A, Postier RG, Umar S, Zhang Y, Anant S. Honokiol radiosensitizes colorectal cancer cells: enhanced activity in cells with mismatch repair defects. Am J Physiol Gastrointest Liver Physiol 301: G929-G937, 2011. First published August 11, 2011; doi:10.1152/ajpgi.00159.2011.-DNA mismatch repair is required for correcting any mismatches that are created during replication and recombination, and a defective mismatch repair system contributes to DNA damage-induced growth arrest. The colorectal cancer cell line HCT116 is known to have a mutation in the hMLH1 mismatch repair gene resulting in microsatellite instability and defective mismatch repair. Honokiol is a biphenolic compound that has been used in traditional Chinese medicine for treating various ailments including cancer. This study was designed to test the hypothesis that honokiol enhances the radiosensitivity of cancer cells with mismatch repair defect (HCT116) compared with those that are mismatch repair proficient (HCT116-CH3). We first determined that the combination of honokiol and gamma-irradiation treatment resulted in dose-dependent inhibition of proliferation and colony formation in both cell lines. However, the effects were more pronounced in HCT116 cells. Similarly, the combination induced higher levels of apoptosis (caspase 3 activation, Bax to Bcl2 ratio) in the HCT116 cells compared with HCT116-CH3 cells. Cell cycle analyses revealed higher levels of dead cells in HCT116 cells. The combination treatment reduced expression of cyclin A1 and D1 and increased phosphorylated p53 in both cell lines, although there were significantly lower amounts of phosphorylated p53 in the HCT116-CH3 cells, suggesting that high levels of hMLH1 reduce radiosensitivity. These data demonstrate that honokiol is highly effective in radiosensitizing colorectal cancer cells, especially those with a mismatch repair defect.
引用
收藏
页码:G929 / G937
页数:9
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