Kim Jin Won, Kim Hwang-Phill, Im Seock-Ah, Kang Soyeong, Hur Hyung Seok, Yoon Young-Kwang, Oh Do-Youn, Kim Jee Hyun, Lee Dong Soon, Kim Tae-You, Bang Yung-Jue
Department of Internal Medicine, Seoul National University College of Medicine, 28 Yongon-dong, Chongno-gu, Seoul 110-744, Republic of Korea.
Cancer Lett. 2008 Dec 18;272(2):296-306. doi: 10.1016/j.canlet.2008.07.018. Epub 2008 Sep 6.
HER2 overexpression is observed in 5-25% of gastric cancers. Lapatinib is a dual inhibitor of the epidermal growth factor receptor and HER2 tyrosine kinase. We examined the antitumor effect of lapatinib in gastric cancer cell lines. Lapatinib induced selective and potent growth inhibition in two HER2-amplified gastric cancer cell lines (SNU-216 and NCI-N87). Lapatinib inhibited the phosphorylation of HER2, EGFR and downstream signaling proteins, resulting in G1 arrest in both cell lines with down-regulation of cMyc and induction of p27kip1. Lapatinib also induced apoptosis in NCI-N87 which has high HER2 amplification ratio. Lapatinib combined with 5-fluorouracil, cisplatin, oxaliplatin or paclitaxel showed an additive or synergistic effect. These results provide a rationale for the future clinical trials of lapatinib combined with cytotoxic drugs in the treatment of HER2-positive gastric cancer.
在5%-25%的胃癌中观察到HER2过表达。拉帕替尼是表皮生长因子受体和HER2酪氨酸激酶的双重抑制剂。我们研究了拉帕替尼对胃癌细胞系的抗肿瘤作用。拉帕替尼在两种HER2扩增的胃癌细胞系(SNU-216和NCI-N87)中诱导了选择性且强效的生长抑制。拉帕替尼抑制了HER2、表皮生长因子受体(EGFR)及下游信号蛋白的磷酸化,导致两个细胞系均出现G1期阻滞,同时cMyc表达下调且p27kip1表达上调。拉帕替尼还诱导了HER2扩增率高的NCI-N87细胞系发生凋亡。拉帕替尼与5-氟尿嘧啶、顺铂、奥沙利铂或紫杉醇联合使用显示出相加或协同效应。这些结果为未来开展拉帕替尼联合细胞毒性药物治疗HER2阳性胃癌的临床试验提供了理论依据。