Singh Ankur, Brito Ilana, Lammerding Jan
Nancy E. and Peter C. Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA; Sibley School of Mechanical and Aerospace Engineering, Cornell University, Ithaca, NY, USA; Caryl and Israel Englander Institute for Precision Medicine, New York Presbyterian Hospital-Weill Cornell Medicine, New York, NY, USA.
Nancy E. and Peter C. Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
Trends Cancer. 2018 Apr;4(4):281-291. doi: 10.1016/j.trecan.2018.01.008. Epub 2018 Mar 10.
Resistance to chemotherapy and pathway-targeted therapies poses a major problem in cancer research. While the fields of tumor biology and experimental therapeutics have already benefited from ex vivo preclinical tissue models, these models have yet to address the reasons for malignant transformations and the emergence of chemoresistance. With the increasing number of ex vivo models poised to incorporate physiological biophysical properties, along with the advent of genomic sequencing information, there are now unprecedented opportunities to better understand tumorigenesis and to design therapeutic approaches to overcome resistance. Here we discuss that new preclinical ex vivo models should consider - in addition to common biophysical parameters such as matrix stiffness and bioadhesivity - a more comprehensive milieu of tissue signaling, nuclear mechanics, immune response, and the gut microbiome.
对化疗和通路靶向治疗的耐药性是癌症研究中的一个主要问题。虽然肿瘤生物学和实验治疗学领域已经从离体临床前组织模型中受益,但这些模型尚未解决恶性转化和化疗耐药性出现的原因。随着越来越多的离体模型准备纳入生理生物物理特性,以及基因组测序信息的出现,现在有前所未有的机会更好地理解肿瘤发生,并设计克服耐药性的治疗方法。在这里,我们讨论新的临床前离体模型除了应考虑诸如基质硬度和生物粘附性等常见生物物理参数外,还应考虑更全面的组织信号传导、核力学、免疫反应和肠道微生物群环境。