Tseng Chia-Hsuan, Huang Wan-Ting, Chew Chee Ho, Lai Jun-Kai, Tu Shih-Hsin, Wei Po-Li, Lee Kang-Yun, Lai Gi-Ming, Chen Chien-Chung
Graduate Institute of Biomedical Materials & Tissue Engineering, Taipei Medical University, Xinyi District, Taipei 11031, Taiwan.
MTAMTech corporation, 17th floor, 3rd Yuanqu Street, Nangang District, Taipei 11503, Taiwan.
Materials (Basel). 2019 Feb 14;12(4):569. doi: 10.3390/ma12040569.
The advent of personalized cancer treatment resulted in the shift from the administration of cytotoxic drugs with broad activity spectrum to a targeted tumor-specific therapy. Aligned to this development, the focus of this study revolved around the application of our novel and patented microtube array membrane (MTAM) in the US National Cancer Institute (NCI) developed an HFA (hollow fiber assay) assay; hereinafter known as MTAM/HFA. Electrospun poly-L-lactic acid (PLLA) MTAM was sterilized and loaded with cell lines/patient derived tumor cells (PDTC) and subcutaneously implanted into the backs of BALB/C mice. Anticancer drugs were administered at the respective time points and the respective MTAMs were retrieved and the viability tumor cells within were quantified with the MTT assay. Results revealed that the MTAMs were excellent culture substrate for various cancer cell lines and PDTCs (patient derived tumor cells). Compared to traditional HFA systems that utilize traditional hollow fibers, MTAM/HFA revealed superior drug sensitivity for a wide range of anticancer drug classes. Additionally, the duration for each test was <14 days; all this while capable of producing similar trend outcome to the current gold-standard xenograft models. These benefits were observed in both the in vitro and in vivo stages, making it a highly practical phenotypic-based solution that could potentially be applied in personalized medicine.
个性化癌症治疗的出现导致了从使用具有广泛活性谱的细胞毒性药物向靶向肿瘤特异性治疗的转变。与此发展相一致,本研究的重点围绕我们新型的、已获专利的微管阵列膜(MTAM)在美国国立癌症研究所(NCI)开发的中空纤维分析(HFA)中的应用展开;以下简称为MTAM/HFA。将静电纺丝聚-L-乳酸(PLLA)MTAM进行灭菌处理,并接种细胞系/患者来源的肿瘤细胞(PDTC),然后皮下植入BALB/C小鼠的背部。在各个时间点给予抗癌药物,随后取回各个MTAM,并通过MTT法对其中存活的肿瘤细胞进行定量分析。结果显示,MTAM是各种癌细胞系和PDTC的优良培养底物。与使用传统中空纤维的传统HFA系统相比,MTAM/HFA对多种抗癌药物类别显示出更高的药物敏感性。此外,每次测试的持续时间<14天;与此同时,能够产生与当前金标准异种移植模型相似的趋势结果。这些优势在体外和体内阶段均有体现,使其成为一种极具实用性且基于表型的解决方案,有望应用于个性化医疗。