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논문 기본 정보

자료유형
학술저널
저자정보
Gu, Wei-Guang (Department of Medical Oncology, Nanhai District People's Hospital) Huang, Yan (Department of Medical Oncology, Sun Yat-Sen University Cancer Center) Yuan, Zhong-Yu (Department of Medical Oncology, Sun Yat-Sen University Cancer Center) Peng, Rou-Jun (Department of Medical Oncology, Sun Yat-Sen University Cancer Center) Luo, Hai-Tao (Department of Medical Oncology, Nanhai District People's Hospital) He, Zhi-Ren (Department of Medical Oncology, Nanhai District People's Hospital) Wang, Shu-Sen (Department of Medical Oncology, Sun Yat-Sen University Cancer Center)
저널정보
아시아태평양암예방학회 Asian Pacific journal of cancer prevention : APJCP Asian Pacific journal of cancer prevention : APJCP 제14권 제3호
발행연도
2013.1
수록면
1,787 - 1,790 (4page)

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This study evaluated the effects of ZD1839, an orally active, selective epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor, on nasopharyngeal carcinoma (NPC) both in vitro and in vivo. Influence of ZD1839 alone or combined with cisplatin on the NPC cell line CNE2 was detected by MTT assay with flow cytometry assessment of cell cycle distribution and apoptosis rates. Nude mice NPC xenografts were also used to evaluate the effects of ZD1839 alone or combined with cisplatin. The Student's t test evaluated statistical significance. ZD1839 alone or combined with cisplatin inhibited CNE2 cell line proliferation. ZD1839 induced CNE2 cell cycle arrest in the G1 phase, and higher concentrations induced apoptosis. Xenograft tumors were significantly smaller when treated with 200 mg/kg ZD1839, cisplatin, or cisplatin combined with 100 mg/kg ZD1839 than untreated controls. ZD1839 (200 mg/kg) alone showed good tumor inhibition effects, reduction of tumor weights, and smaller tumor volume without loss of body weight. ZD1839 (200 mg/kg) might provide a good and effective therapeutic reagent for NPC.

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