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Single-cell transcriptomic analysis of normal and pathological tissues from the same patient uncovers colon cancer progression
The aim of the present study was to elucidate the evolutionary trajectory of colon cells from normal colon mucosa, to adenoma, then to carcinoma in the same microenvironment. Normal colon, adenoma and carcinoma tissues from the same patient were analyzed by single-cell sequencing, which perfectly si...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031920/ https://www.ncbi.nlm.nih.gov/pubmed/36944972 http://dx.doi.org/10.1186/s13578-023-01002-w |
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author | Sun, Ruifang Yang, Yang Lü, Weidong Yang, Yanqi Li, Yulong Liu, Zhigang Diao, Dongmei Wang, Yang Chang, Su’e Lu, Mengnan Jiang, Qiuyu Dai, Bingling Ma, Xiaobin Zhao, Chang’an Lü, Moqi Zhang, Juan Ding, Caixia Li, Na Zhang, Jian Xiao, Zhengtao Zhou, Dangxia Huang, Chen |
author_facet | Sun, Ruifang Yang, Yang Lü, Weidong Yang, Yanqi Li, Yulong Liu, Zhigang Diao, Dongmei Wang, Yang Chang, Su’e Lu, Mengnan Jiang, Qiuyu Dai, Bingling Ma, Xiaobin Zhao, Chang’an Lü, Moqi Zhang, Juan Ding, Caixia Li, Na Zhang, Jian Xiao, Zhengtao Zhou, Dangxia Huang, Chen |
author_sort | Sun, Ruifang |
collection | PubMed |
description | The aim of the present study was to elucidate the evolutionary trajectory of colon cells from normal colon mucosa, to adenoma, then to carcinoma in the same microenvironment. Normal colon, adenoma and carcinoma tissues from the same patient were analyzed by single-cell sequencing, which perfectly simulated the process of time-dependent colon cancer due to the same microenvironment. A total of 22 cell types were identified. Results suggest the presence of dominant clones of same cells including C2 goblet cell, epithelial cell subtype 1 (Epi1), enterocyte cell subset 0 (Entero0), and Entero5 in carcinoma. Epi1 and Entero0 were Co-enriched in antibacterial and IL-17 signaling, Entero5 was enriched in immune response and mucin-type O-glycan biosynthesis. We discovered new colon cancer related genes including AC007952.4, NEK8, CHRM3, ANO7, B3GNT6, NEURL1, ODC1 and KCNMA1. The function of TBC1D4, LTB, C2CD4A, AND GBP4/5 in T cells needs to be clarified. We used colon samples from the same person, which provide new information for colon cancer therapy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13578-023-01002-w. |
format | Online Article Text |
id | pubmed-10031920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100319202023-03-23 Single-cell transcriptomic analysis of normal and pathological tissues from the same patient uncovers colon cancer progression Sun, Ruifang Yang, Yang Lü, Weidong Yang, Yanqi Li, Yulong Liu, Zhigang Diao, Dongmei Wang, Yang Chang, Su’e Lu, Mengnan Jiang, Qiuyu Dai, Bingling Ma, Xiaobin Zhao, Chang’an Lü, Moqi Zhang, Juan Ding, Caixia Li, Na Zhang, Jian Xiao, Zhengtao Zhou, Dangxia Huang, Chen Cell Biosci Research The aim of the present study was to elucidate the evolutionary trajectory of colon cells from normal colon mucosa, to adenoma, then to carcinoma in the same microenvironment. Normal colon, adenoma and carcinoma tissues from the same patient were analyzed by single-cell sequencing, which perfectly simulated the process of time-dependent colon cancer due to the same microenvironment. A total of 22 cell types were identified. Results suggest the presence of dominant clones of same cells including C2 goblet cell, epithelial cell subtype 1 (Epi1), enterocyte cell subset 0 (Entero0), and Entero5 in carcinoma. Epi1 and Entero0 were Co-enriched in antibacterial and IL-17 signaling, Entero5 was enriched in immune response and mucin-type O-glycan biosynthesis. We discovered new colon cancer related genes including AC007952.4, NEK8, CHRM3, ANO7, B3GNT6, NEURL1, ODC1 and KCNMA1. The function of TBC1D4, LTB, C2CD4A, AND GBP4/5 in T cells needs to be clarified. We used colon samples from the same person, which provide new information for colon cancer therapy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13578-023-01002-w. BioMed Central 2023-03-21 /pmc/articles/PMC10031920/ /pubmed/36944972 http://dx.doi.org/10.1186/s13578-023-01002-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Sun, Ruifang Yang, Yang Lü, Weidong Yang, Yanqi Li, Yulong Liu, Zhigang Diao, Dongmei Wang, Yang Chang, Su’e Lu, Mengnan Jiang, Qiuyu Dai, Bingling Ma, Xiaobin Zhao, Chang’an Lü, Moqi Zhang, Juan Ding, Caixia Li, Na Zhang, Jian Xiao, Zhengtao Zhou, Dangxia Huang, Chen Single-cell transcriptomic analysis of normal and pathological tissues from the same patient uncovers colon cancer progression |
title | Single-cell transcriptomic analysis of normal and pathological tissues from the same patient uncovers colon cancer progression |
title_full | Single-cell transcriptomic analysis of normal and pathological tissues from the same patient uncovers colon cancer progression |
title_fullStr | Single-cell transcriptomic analysis of normal and pathological tissues from the same patient uncovers colon cancer progression |
title_full_unstemmed | Single-cell transcriptomic analysis of normal and pathological tissues from the same patient uncovers colon cancer progression |
title_short | Single-cell transcriptomic analysis of normal and pathological tissues from the same patient uncovers colon cancer progression |
title_sort | single-cell transcriptomic analysis of normal and pathological tissues from the same patient uncovers colon cancer progression |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031920/ https://www.ncbi.nlm.nih.gov/pubmed/36944972 http://dx.doi.org/10.1186/s13578-023-01002-w |
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