间质细胞
肿瘤微环境
免疫系统
血管生成
癌症研究
肝细胞癌
背景(考古学)
癌细胞
生物
细胞
转录组
医学
病理
癌症
免疫学
基因表达
基因
遗传学
古生物学
作者
Joseph W. Franses,Irun Bhan,Cristina R. Ferrone,Genevieve M. Boland,David T. Ting
标识
DOI:10.1200/jco.2022.40.16_suppl.e16110
摘要
e16110 Background: The microenvironment within hepatocellular carcinoma (HCC) tumors is composed of interacting cancer cells, endothelial cells and other stromal cells, and immune cells. The emerging field of spatial transcriptomics enables the measurement of gene expression in specific regions within a tissue sample. This technique retains the spatial context of intact tissue, can provide deep biological insights into cell-cell interactions, tumor microenvironment, and tumor progression. Methods: Resolve Biosciences’ Molecular Cartography platform was used on serial fresh frozen sections obtained from treatment naïve, HCC samples, and matched non-cancerous control liver tissues. Results: Given the high sensitivity, single-cell resolution, and specificity of the platform, the gene profiles of the hepatic endothelial, mesenchymal and parenchymal cell were studied in-depth to characterize the tumor microenvironment. The data obtained from the analyses revealed several local interactions between cancer cells, endothelial cells, and immune cells. These interactions include both known immune checkpoints and angiogenesis drivers and novel interactions. Conclusions: A deeper in situ understanding of the interacting cellular components of the HCC microenvironment may give insight into the natural history (prognosis) of the disease, predict response to therapies that target the immune system and vasculature, and define novel targets for the next generation of drug development.
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