Classification of lung adenocarcinoma based on stemness scores in bulk and single cell transcriptomes

被引:6
|
作者
Liu, Qian [1 ,2 ,3 ]
Lei, Jiali [1 ,2 ,3 ]
Zhang, Xiaobo [4 ]
Wang, Xiaosheng [1 ,2 ,3 ]
机构
[1] China Pharmaceut Univ, Sch Basic Med & Clin Pharm, Biomed Informat Res Lab, Nanjing 211198, Peoples R China
[2] China Pharmaceut Univ, Canc Genom Res Ctr, Sch Basic Med & Clin Pharm, Nanjing 211198, Peoples R China
[3] China Pharmaceut Univ, Big Data Res Inst, Nanjing 211198, Peoples R China
[4] China Pharmaceut Univ, Sch Basic Med & Clin Pharm, Jiangsu Key Lab Carcinogenesis & Intervent, Nanjing 210009, Peoples R China
关键词
Lung adenocarcinoma; Tumor stemness; Subtyping; Transcriptome; Clustering analysis; Immunotherapy and targeted therapy; INTRATUMORAL HETEROGENEITY; IMMUNE EVASION; CANCER; TUMOR; METASTASIS; SIGNATURES; LANDSCAPE; MUTATION;
D O I
10.1016/j.csbj.2022.04.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tumor stemness is associated with tumor progression and therapy resistance. The recent advances in sequencing, genomics, and computational technologies have facilitated investigation into the tumor stemness cell-like characteristics. We identified subtypes of lung adenocarcinoma (LUAD) in bulk tumors or single cells based on the enrichment scores of 12 stemness signatures by clustering analysis of their transcriptomic profiles. Three stemness subtypes of LUAD were identified: St-H, St-M, and St-L, having high, medium, and low stemness signatures, respectively, consistently in six different datasets. Among the three subtypes, St-H was the most enriched in epithelial-mesenchymal transition, invasion, and metastasis signaling, genomically instable, irresponsive to immunotherapies and targeted therapies, and hence had the worst prognosis. We observed that intratumor heterogeneity was significantly higher in high-stemness than in low-stemness bulk tumors, but significantly lower in high-stemness than in low-stemness single cancer cells. Moreover, tumor immunity was stronger in high-stemness than in low-stemness cancer cells, but weaker in high-stemness than in low-stemness bulk tumors. These differences between bulk tumors and single cancer cells could be attributed to the non-tumor cells in bulk tumors that confounded the results of correlation analysis. Furthermore, pseudotime analysis showed that many St-H cells were at the beginning of the cell evolution trajectory, compared to most St-L cells in the terminal or later phase, suggesting that many low-stemness cells are originated from highstemness cells. The stemness-based classification of LUAD may provide novel insights into the tumor biology as well as precise clinical management of this disease. (c) 2022 Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/ licenses/by-nc-nd/4.0/).
引用
收藏
页码:1691 / 1701
页数:11
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