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白头翁皂苷D(SB365)可抑制具有Met扩增的吉非替尼耐药非小细胞肺癌细胞的生长。

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

作者信息

Jang Won-Jun, Park Byoungduck, Jeong Gil-Saeng, Hong Soon-Sun, Jeong Chul-Ho

机构信息

College of Pharmacy, Keimyung University, Daegu 704-701, Republic of Korea.

Department of Biomedical Sciences, College of Medicine, Inha University, Incheon, Republic of Korea.

出版信息

Oncol Rep. 2014 Dec;32(6):2612-8. doi: 10.3892/or.2014.3528. Epub 2014 Oct 3.

Abstract

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.

摘要

使用吉非替尼或厄洛替尼等表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)的临床治疗已应用于非小细胞肺癌(NSCLC)患者。不幸的是,由于Met原癌基因的扩增,这些患者会出现获得性耐药,这可能是非小细胞肺癌对抗EGFR抑制的一种补偿机制。为了克服这种耐药性,鉴定新的小分子天然化合物对癌症治疗至关重要。在这方面,SB365,即朝鲜白头翁根中的皂苷D,在韩国作为治疗多种疾病的传统药物,已引起广泛关注。在本研究中,SB365有效抑制了具有Met扩增的吉非替尼耐药HCC827GR NSCLC细胞的增殖。值得注意的是,我们的数据显示SB365抑制了Met的磷酸化以及Met扩增的HCC827GR细胞生长和存活所需的下游信号通路。此外,SB365抑制了HCC827GR细胞的非锚定依赖性生长、迁移和侵袭,并诱导了细胞凋亡。因此,这些结果表明SB365是用于治疗Met扩增的非小细胞肺癌的天然产物的良好候选者。

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