Sakamoto Yasunari, Yamagishi Seri, Tanizawa Yoshinori, Tajimi Masaomi, Okusaka Takuji, Ojima Hidenori
Department of Hepatobiliary and Pancreatic Oncology, Tokyo, National Cancer Center Hospital.
Division of Cancer Genomics, National Cancer Center Research Institute, Tokyo.
Jpn J Clin Oncol. 2018 Apr 1;48(4):396-399. doi: 10.1093/jjco/hyy011.
Biliary tract carcinoma (BTC) is an extremely malignant tumor, but available treatment options are limited. Despite of needs for novel therapies, few BTC-related resources are currently available for evaluation of candidate drugs. To address this issue, we have recently established 13 cell lines from surgical specimens from Japanese BTC patients. In the present study, we evaluated four new molecular targeting agents using our BTC cell-based assay panel with 17 BTC cell lines. PI3K/mTOR dual inhibitor LY3023414 showed activity at submicromolar concentration ranges against 13 of the 17 cell lines tested, including the ones with gemcitabine insensitivity. In conclusion, we demonstrated that in vitro study with the BTC cell line panel would be an efficient approach to screen for novel therapeutic strategies. Although this is preliminary result and further investigations are required for confirmation, PI3K/mTOR inhibitor might be a potential target for BTC drug development.
胆管癌(BTC)是一种极具恶性的肿瘤,但现有的治疗选择有限。尽管需要新的治疗方法,但目前几乎没有与BTC相关的资源可用于评估候选药物。为了解决这个问题,我们最近从日本BTC患者的手术标本中建立了13种细胞系。在本研究中,我们使用我们基于BTC细胞的检测平台和17种BTC细胞系评估了四种新的分子靶向药物。PI3K/mTOR双重抑制剂LY3023414在亚微摩尔浓度范围内对17种测试细胞系中的13种显示出活性,包括对吉西他滨不敏感的细胞系。总之,我们证明了使用BTC细胞系进行体外研究将是筛选新治疗策略的有效方法。虽然这是初步结果,需要进一步研究来证实,但PI3K/mTOR抑制剂可能是BTC药物开发的潜在靶点。