生物
核糖核酸
病理
间隙
免疫荧光
细胞
癌症
癌细胞
计算生物学
基因表达
细胞生物学
医学
基因
抗体
遗传学
泌尿科
作者
Nobuyuki Tanaka,Shigeaki Kanatani,Dagmara Kaczyńska,Keishiro Fukumoto,Lauri Louhivuori,Tomohiro Mizutani,Oded Kopper,Pauliina Kronqvist,Stephanie Robertson,Claes Lindh,Lóránd Kis,Robin Pronk,Naoya Niwa,Kazuhiro Matsumoto,Mototsugu Oya,Ayako Miyakawa,Anna Falk,Johan Hartman,Cecilia Sahlgren,Hans Clevers,Per Uhlén
标识
DOI:10.1038/s41551-020-0576-z
摘要
Microscopy analysis of tumour samples is commonly performed on fixed, thinly sectioned and protein-labelled tissues. However, these examinations do not reveal the intricate three-dimensional structures of tumours, nor enable the detection of aberrant transcripts. Here, we report a method, which we name DIIFCO (for diagnosing in situ immunofluorescence-labelled cleared oncosamples), for the multimodal volumetric imaging of RNAs and proteins in intact tumour volumes and organoids. We used DIIFCO to spatially profile the expression of diverse coding RNAs and non-coding RNAs at the single-cell resolution in a variety of cancer tissues. Quantitative single-cell analysis revealed spatial niches of cancer stem-like cells, and showed that the niches were present at a higher density in triple-negative breast cancer tissue. The improved molecular phenotyping and histopathological diagnosis of cancers may lead to new insights into the biology of tumours of patients.
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