Integrated single-cell transcriptome analysis reveals heterogeneity of esophageal squamous cell carcinoma microenvironment

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作者
Huy Q. Dinh
Feng Pan
Geng Wang
Qing-Feng Huang
Claire E. Olingy
Zhi-Yong Wu
Shao-Hong Wang
Xin Xu
Xiu-E Xu
Jian-Zhong He
Qian Yang
Sandra Orsulic
Marcela Haro
Li-Yan Li
Guo-Wei Huang
Joshua J. Breunig
H. Phillip Koeffler
Catherine C. Hedrick
Li-Yan Xu
De-Chen Lin
En-Min Li
机构
[1] University of Wisconsin-Madison School of Medicine and Public Health,McArdle Laboratory for Cancer Research
[2] La Jolla Institute for Immunology,Division of Inflammation Biology
[3] Shantou University Medical College,Guangdong Provincial Key Laboratory of Infectious Diseases and Molecular Immunopathology, The Key Laboratory of Molecular Biology for High Cancer Incidence Coastal Chaoshan Area
[4] Guangdong Esophageal Cancer Research Institute,Department of Thoracic Surgery
[5] Shantou Sub-center,Department of Medicine
[6] Cancer Hospital of Shantou University Medical College,Department of Obstetrics and Gynecology and Samuel Oschin Comprehensive Cancer Institute
[7] Shantou Central Hospital,Board of Governors Regenerative Medicine Institute and Department of Biomedical Sciences
[8] Samuel Oschin Comprehensive Cancer Institute,undefined
[9] Cedars-Sinai Medical Center,undefined
[10] Cedars-Sinai Medical Center,undefined
[11] David Geffen School of Medicine at UCLA,undefined
[12] Cedars-Sinai Medical Center,undefined
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摘要
The tumor microenvironment is a highly complex ecosystem of diverse cell types, which shape cancer biology and impact the responsiveness to therapy. Here, we analyze the microenvironment of esophageal squamous cell carcinoma (ESCC) using single-cell transcriptome sequencing in 62,161 cells from blood, adjacent nonmalignant and matched tumor samples from 11 ESCC patients. We uncover heterogeneity in most cell types of the ESCC stroma, particularly in the fibroblast and immune cell compartments. We identify a tumor-specific subset of CST1+ myofibroblasts with prognostic values and potential biological significance. CST1+ myofibroblasts are also highly tumor-specific in other cancer types. Additionally, a subset of antigen-presenting fibroblasts is revealed and validated. Analyses of myeloid and T lymphoid lineages highlight the immunosuppressive nature of the ESCC microenvironment, and identify cancer-specific expression of immune checkpoint inhibitors. This work establishes a rich resource of stromal cell types of the ESCC microenvironment for further understanding of ESCC biology.
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