| Literature DB >> 32601394 |
Nobuyuki Tanaka1,2, Shigeaki Kanatani3, Dagmara Kaczynska3, Keishiro Fukumoto3,4, Lauri Louhivuori3, Tomohiro Mizutani5, Oded Kopper5, Pauliina Kronqvist6, Stephanie Robertson7,8, Claes Lindh7,8, Lorand Kis7,8, Robin Pronk9, Naoya Niwa4, Kazuhiro Matsumoto4, Mototsugu Oya4, Ayako Miyakawa3,10, Anna Falk9, Johan Hartman7,8, Cecilia Sahlgren11,12,5, Hans Clevers5, Per Uhlén13.
Abstract
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.Entities:
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Year: 2020 PMID: 32601394 DOI: 10.1038/s41551-020-0576-z
Source DB: PubMed Journal: Nat Biomed Eng ISSN: 2157-846X Impact factor: 25.671