类有机物
胰腺癌
蛋白质组学
计算生物学
计算机科学
生物
内科学
癌症
医学
细胞生物学
生物化学
基因
作者
Ronnie Ren Jie Low,Ka Yee Fung,Laura F. Dagley,Jumana Yousef,Samantha J. Emery‐Corbin,Tracy L. Putoczki
标识
DOI:10.1007/978-1-0716-3922-1_6
摘要
Pancreatic ductal adenocarcinoma (PDAC) is a lethal solid malignancy with many patients succumbing to the disease within 6 months of diagnosis. The mechanisms that underlie PDAC initiation and progression are poorly understood. Current treatment options are primarily limited to chemotherapy, which is often provided with palliative intent. Unfortunately, there are no robust biomarkers to guide treatment selection or monitor treatment response. This is concerning given the increasing incidence of this cancer. We and others have generated organoid models to explore the biology underlying PDAC with the goal of identifying new therapeutic targets. Here we provide protocols to generate a preclinical PDAC organoid model and methods to use these to define the proteomic landscape of this cancer.
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