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通过癌症原位小鼠模型中的彩色编码成像可视化肿瘤微环境。

Visualizing the Tumor Microenvironment by Color-coded Imaging in Orthotopic Mouse Models of Cancer.

作者信息

Suetsugu Atsushi, Shimizu Masahito, Saji Shigetoyo, Moriwaki Hisataka, Hoffman Robert M

机构信息

Gifu University, Graduate School of Medicine, Gifu, Japan

AntiCancer, Inc., San Diego, CA, U.S.A.

出版信息

Anticancer Res. 2018 Apr;38(4):1847-1857. doi: 10.21873/anticanres.12423.

Abstract

The tumor microenvironment (TME) contains stromal cells in a complex interaction with cancer cells. This relationship has become better understood with the use of fluorescent proteins for in vivo imaging, originally developed by our laboratories. Spectrally-distinct fluorescent proteins can used for color-coded imaging of the complex interaction of the tumor microenvironment in the living state using cancer cells expressing a fluorescent protein of one color and host mice expressing another-color fluorescent protein. Cancer cells engineered in vitro to express a fluorescent protein were orthotopically implanted into transgenic mice expressing a fluorescent protein of a different color. Confocal microscopy was then used for color-coded imaging of the TME. Color-coded imaging of the TME has enabled us to discover that stromal cells are necessary for metastasis. Patient-derived orthotopic xenograft (PDOX) tumors were labeled by first passaging them orthotopically through transgenic nude mice expressing either green, red, or cyan fluorescent protein in order to label the stromal cells of the tumor. The colored stromal cells become stably associated with the PDOX tumors through multiple passages in transgenic colored mice or non-colored mice. The fluorescent protein-expressing stromal cells included cancer-associated fibroblasts and tumor-associated macrophages. The cancer cells in PDOX models can also be labeled with a telomerase-dependent adenovirus containing the gene for green fluorescent protein. Using this model, specific cancer-cell or stromal-cell targeting by potential therapeutics can be visualized. Color-coded imaging enabled the visualization of apparent fusion of cancer and stromal cells. Color-coded imaging is a powerful tool visualizing the interaction of cancer and stromal cells during cancer progression and treatment.

摘要

肿瘤微环境(TME)包含与癌细胞发生复杂相互作用的基质细胞。随着最初由我们实验室开发的用于体内成像的荧光蛋白的应用,这种关系已得到更好的理解。光谱不同的荧光蛋白可用于对处于活体状态的肿瘤微环境的复杂相互作用进行颜色编码成像,方法是让癌细胞表达一种颜色的荧光蛋白,宿主小鼠表达另一种颜色的荧光蛋白。体外经基因工程改造以表达荧光蛋白的癌细胞被原位植入表达不同颜色荧光蛋白的转基因小鼠体内。然后使用共聚焦显微镜对TME进行颜色编码成像。TME的颜色编码成像使我们发现基质细胞对转移是必需的。通过将患者来源的原位异种移植(PDOX)肿瘤首先原位传代接种到表达绿色、红色或青色荧光蛋白的转基因裸鼠体内,以标记肿瘤的基质细胞。通过在转基因有色小鼠或无色小鼠中多次传代,这些带颜色的基质细胞与PDOX肿瘤稳定地结合在一起。表达荧光蛋白的基质细胞包括癌症相关成纤维细胞和肿瘤相关巨噬细胞。PDOX模型中的癌细胞也可用含有绿色荧光蛋白基因的端粒酶依赖性腺病毒进行标记。利用该模型,可以可视化潜在治疗药物对特定癌细胞或基质细胞的靶向作用。颜色编码成像能够观察到癌细胞与基质细胞明显的融合。颜色编码成像是一种强大的工具,可用于观察癌症进展和治疗过程中癌细胞与基质细胞的相互作用。

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