SB365, Pulsatilla saponin D, suppresses the growth of gefitinib-resistant NSCLC cells with Met amplification

被引:8
|
作者
Jang, Won-Jun [1 ]
Park, Byoungduck [1 ]
Jeong, Gil-Saeng [1 ]
Hong, Soon-Sun [2 ]
Jeong, Chul-Ho [1 ]
机构
[1] Keimyung Univ, Coll Pharm, Taegu 704701, South Korea
[2] Inha Univ, Coll Med, Dept Biomed Sci, Inchon, South Korea
关键词
SB365; saponin D; gefitinib; drug resistance; EGFR; Met; LUNG-CANCER; FACTOR RECEPTOR; PANCREATIC-CANCER; EGFR; MUTATIONS; APOPTOSIS; PROLIFERATION; ANGIOGENESIS; STATISTICS; ERLOTINIB;
D O I
10.3892/or.2014.3528
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Clinical treatment using epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) such as gefitinib or erlotinib has been applied in patients with non-small cell lung cancers (NSCLCs). Unfortunately, acquired drug resistance emerges in these patients due to the amplification of the Met proto-oncogene, which may be a compensatory mechanism of NSCLCs against EGFR inhibition. To overcome this resistance, identification of new small-molecule natural compounds is crucial for cancer therapeutics. In this regard, SB365, saponin D from the root of Pulsatilla koreana which has been used as a traditional medicine in Korea for several diseases, has attracted wide interest. In the present study, SB365 effectively suppressed the proliferation of gefitinib-resistant HCC827GR NSCLC cells with Met amplification. Notably, our data revealed that SB365 inhibited the phosphorylation of Met and the downstream signaling pathway required for growth and survival in the Met-amplified HCC827GR cells. Moreover, SB365 suppressed the anchorage-independent growth, migration and invasion along with induction of apoptosis in the HCC827GR cells. Therefore, these results suggest that SB365 is good candidate as a natural product for use in the treatment of Met-amplified NSCLCs.
引用
收藏
页码:2612 / 2618
页数:7
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