Nature Communications (Dec 2023)
Single cell multi-omics reveal intra-cell-line heterogeneity across human cancer cell lines
- Qionghua Zhu,
- Xin Zhao,
- Yuanhang Zhang,
- Yanping Li,
- Shang Liu,
- Jingxuan Han,
- Zhiyuan Sun,
- Chunqing Wang,
- Daqi Deng,
- Shanshan Wang,
- Yisen Tang,
- Yaling Huang,
- Siyuan Jiang,
- Chi Tian,
- Xi Chen,
- Yue Yuan,
- Zeyu Li,
- Tao Yang,
- Tingting Lai,
- Yiqun Liu,
- Wenzhen Yang,
- Xuanxuan Zou,
- Mingyuan Zhang,
- Huanhuan Cui,
- Chuanyu Liu,
- Xin Jin,
- Yuhui Hu,
- Ao Chen,
- Xun Xu,
- Guipeng Li,
- Yong Hou,
- Longqi Liu,
- Shiping Liu,
- Liang Fang,
- Wei Chen,
- Liang Wu
Affiliations
- Qionghua Zhu
- Shenzhen Key Laboratory of Gene Regulation and Systems Biology, School of Life Sciences, Southern University of Science and Technology
- Xin Zhao
- BGI Research
- Yuanhang Zhang
- BGI Research
- Yanping Li
- Department of Systems Biology, School of Life Sciences, Southern University of Science and Technology
- Shang Liu
- BGI Research
- Jingxuan Han
- Department of Systems Biology, School of Life Sciences, Southern University of Science and Technology
- Zhiyuan Sun
- Department of Systems Biology, School of Life Sciences, Southern University of Science and Technology
- Chunqing Wang
- BGI Research
- Daqi Deng
- Department of Systems Biology, School of Life Sciences, Southern University of Science and Technology
- Shanshan Wang
- BGI Research
- Yisen Tang
- Department of Systems Biology, School of Life Sciences, Southern University of Science and Technology
- Yaling Huang
- BGI Research
- Siyuan Jiang
- BGI Research
- Chi Tian
- Department of Systems Biology, School of Life Sciences, Southern University of Science and Technology
- Xi Chen
- BGI Research
- Yue Yuan
- BGI Research
- Zeyu Li
- BGI Research
- Tao Yang
- China National GeneBank
- Tingting Lai
- China National GeneBank
- Yiqun Liu
- China National GeneBank
- Wenzhen Yang
- China National GeneBank
- Xuanxuan Zou
- BGI Research
- Mingyuan Zhang
- BGI Research
- Huanhuan Cui
- Shenzhen Key Laboratory of Gene Regulation and Systems Biology, School of Life Sciences, Southern University of Science and Technology
- Chuanyu Liu
- BGI Research
- Xin Jin
- BGI Research
- Yuhui Hu
- Shenzhen Key Laboratory of Gene Regulation and Systems Biology, School of Life Sciences, Southern University of Science and Technology
- Ao Chen
- BGI Research
- Xun Xu
- BGI Research
- Guipeng Li
- Shenzhen Key Laboratory of Gene Regulation and Systems Biology, School of Life Sciences, Southern University of Science and Technology
- Yong Hou
- BGI Research
- Longqi Liu
- BGI Research
- Shiping Liu
- BGI Research
- Liang Fang
- Shenzhen Key Laboratory of Gene Regulation and Systems Biology, School of Life Sciences, Southern University of Science and Technology
- Wei Chen
- Shenzhen Key Laboratory of Gene Regulation and Systems Biology, School of Life Sciences, Southern University of Science and Technology
- Liang Wu
- BGI Research
- DOI
- https://doi.org/10.1038/s41467-023-43991-9
- Journal volume & issue
-
Vol. 14,
no. 1
pp. 1 – 21
Abstract
Abstract Human cancer cell lines have long served as tools for cancer research and drug discovery, but the presence and the source of intra-cell-line heterogeneity remain elusive. Here, we perform single-cell RNA-sequencing and ATAC-sequencing on 42 and 39 human cell lines, respectively, to illustrate both transcriptomic and epigenetic heterogeneity within individual cell lines. Our data reveal that transcriptomic heterogeneity is frequently observed in cancer cell lines of different tissue origins, often driven by multiple common transcriptional programs. Copy number variation, as well as epigenetic variation and extrachromosomal DNA distribution all contribute to the detected intra-cell-line heterogeneity. Using hypoxia treatment as an example, we demonstrate that transcriptomic heterogeneity could be reshaped by environmental stress. Overall, our study performs single-cell multi-omics of commonly used human cancer cell lines and offers mechanistic insights into the intra-cell-line heterogeneity and its dynamics, which would serve as an important resource for future cancer cell line-based studies.