Liliana Sokol
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Liliana Sokol has a total of 104 co-authors. Here are the top co-authors by number of shared publications:
- Peter Carmeliet
Laboratory of Angiogenesis and Vascular Metabolism, Department of Oncology, KU Leuven, Leuven, Belgium
8 shared publications - Joanna Kalucka
Department of Biomedicine, Aarhus University, Aarhus, Denmark
7 shared publications Luc Schoonjans
Laboratory of Angiogenesis and Vascular Metabolism, Center for Cancer Biology, VIB, & Department of Oncology and Leuven Cancer Institute (LKI), KU Leuven, Leuven, Belgium
7 shared publications- Lucas Treps
INSERM UMR 1307, CNRS UMR 6075, Nantes Université, Université d’Angers, Nantes, F-44000, France
7 shared publications - Melissa García-Caballero
Laboratory of Angiogenesis and Vascular Metabolism, VIB Center for Cancer Biology, VIB, Leuven, Belgium
7 shared publications Guy Eelen
Laboratory of Angiogenesis and Vascular Metabolism, Center for Cancer Biology, VIB, Department of Oncology and Leuven Cancer Institute (LKI), KU Leuven, Leuven, Belgium
6 shared publications
Latest Publications
- Open Access
- 6 November 2025
- Published by Elsevier in JHEP Reports
- Vol. 8 (2) , 101668
STAT1 drives the immune landscape of murine Toll-like receptor 9-induced liver inflammation
- 6 November 2025
- Published by Elsevier in JHEP Reports
- Vol. 8 (2) , 101668
Open AccessSTAT1 drives the immune landscape of murine Toll-like receptor 9-induced liver inflammation
- Open Access
- 21 September 2022
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 23 (19) , 11052
Metabolic Reprogramming in Tumor Endothelial Cells
The dynamic crosstalk between the different components of the tumor microenvironment is critical to determine cancer progression, metastatic dissemination, tumor immunity, and therapeutic responses. Angiogenesis is critical for tumor growth, and abnormal blood vessels contribute to hypoxia and acidosis in the tumor microenvironment. In this hostile environment, cancer and stromal cells have the ability to alter their metabolism in order to support the high energetic demands and favor rapid tumor proliferation. Recent advances have shown that tumor endothelial cell metabolism is reprogrammed, and that targeting endothelial metabolic pathways impacts developmental and pathological vessel sprouting. Therefore, the use of metabolic antiangiogenic therapies to normalize the blood vasculature, in combination with immunotherapies, offers a clinical niche to treat cancer.
- 21 September 2022
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 23 (19) , 11052
Open AccessMetabolic Reprogramming in Tumor Endothelial Cells
The dynamic crosstalk between the different components of the tumor microenvironment is critical to determine cancer progression, metastatic dissemination, tumor immunity, and therapeutic responses. Angiogenesis is critical for tumor growth, and abnormal blood vessels contribute to hypoxia and acidosis in the tumor microenvironment. In this hostile environment, cancer and stromal cells have the ability to alter their metabolism in order to support the high energetic demands and favor rapid tumor proliferation. Recent advances have shown that tumor endothelial cell metabolism is reprogrammed, and that targeting endothelial metabolic pathways impacts developmental and pathological vessel sprouting. Therefore, the use of metabolic antiangiogenic therapies to normalize the blood vasculature, in combination with immunotherapies, offers a clinical niche to treat cancer.
- Open Access
- 14 September 2021
- Published by Elsevier in STAR Protocols
- Vol. 2 (3) , 100508
Protocols for endothelial cell isolation from mouse tissues: brain, choroid, lung, and muscle
- 14 September 2021
- Published by Elsevier in STAR Protocols
- Vol. 2 (3) , 100508
Open AccessProtocols for endothelial cell isolation from mouse tissues: brain, choroid, lung, and muscle
- Open Access
- 1 September 2021
- Published by Elsevier in STAR Protocols
- Vol. 2 (3) , 100523
Protocols for endothelial cell isolation from mouse tissues: kidney, spleen, and testis
- 1 September 2021
- Published by Elsevier in STAR Protocols
- Vol. 2 (3) , 100523
Open AccessProtocols for endothelial cell isolation from mouse tissues: kidney, spleen, and testis
- Open Access
- 1 June 2021
- Published by Elsevier in STAR Protocols
- Vol. 2 (2) , 100489
Protocols for endothelial cell isolation from mouse tissues: small intestine, colon, heart, and liver
- 1 June 2021
- Published by Elsevier in STAR Protocols
- Vol. 2 (2) , 100489
Open AccessProtocols for endothelial cell isolation from mouse tissues: small intestine, colon, heart, and liver
- Top Cited Papers
- 1 April 2020
- Published by Elsevier in Cell Metabolism
- Vol. 31 (4) , 862-877.e14
Single-Cell RNA Sequencing Maps Endothelial Metabolic Plasticity in Pathological Angiogenesis
- 1 April 2020
- Published by Elsevier in Cell Metabolism
- Vol. 31 (4) , 862-877.e14
Top Cited PapersSingle-Cell RNA Sequencing Maps Endothelial Metabolic Plasticity in Pathological Angiogenesis
- Top Cited Papers
Single-Cell Transcriptome Atlas of Murine Endothelial Cells
- Top Cited Papers
- 1 January 2020
- Published by Elsevier in Cancer Cell
- Vol. 37 (1) , 21-36.e13
An Integrated Gene Expression Landscape Profiling Approach to Identify Lung Tumor Endothelial Cell Heterogeneity and Angiogenic Candidates
- 1 January 2020
- Published by Elsevier in Cancer Cell
- Vol. 37 (1) , 21-36.e13
Top Cited PapersAn Integrated Gene Expression Landscape Profiling Approach to Identify Lung Tumor Endothelial Cell Heterogeneity and Angiogenic Candidates
- Open Access
- 24 October 2018
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 47 (D1) , D736-D744
EndoDB: a database of endothelial cell transcriptomics data
Endothelial cells (ECs) line blood vessels, regulate homeostatic processes (blood flow, immune cell trafficking), but are also involved in many prevalent diseases. The increasing use of high-throughput technologies such as gene expression microarrays and (single cell) RNA sequencing generated a wealth of data on the molecular basis of EC (dys-)function. Extracting biological insight from these datasets is challenging for scientists who are not proficient in bioinformatics. To facilitate the re-use of publicly available EC transcriptomics data, we developed the endothelial database EndoDB, a web-accessible collection of expert curated, quality assured and pre-analyzed data collected from 360 datasets comprising a total of 4741 bulk and 5847 single cell endothelial transcriptomes from six different organisms. Unlike other added-value databases, EndoDB allows to easily retrieve and explore data of specific studies, determine under which conditions genes and pathways of interest are deregulated and assess reprogramming of metabolism via principal component analysis, differential gene expression analysis, gene set enrichment analysis, heatmaps and metabolic and transcription factor analysis, while single cell data are visualized as gene expression color-coded t-SNE plots. Plots and tables in EndoDB are customizable, downloadable and interactive. EndoDB is freely available at https://vibcancer.be/software-tools/endodb, and will be updated to include new studies.
- 24 October 2018
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 47 (D1) , D736-D744
Open AccessEndoDB: a database of endothelial cell transcriptomics data
Endothelial cells (ECs) line blood vessels, regulate homeostatic processes (blood flow, immune cell trafficking), but are also involved in many prevalent diseases. The increasing use of high-throughput technologies such as gene expression microarrays and (single cell) RNA sequencing generated a wealth of data on the molecular basis of EC (dys-)function. Extracting biological insight from these datasets is challenging for scientists who are not proficient in bioinformatics. To facilitate the re-use of publicly available EC transcriptomics data, we developed the endothelial database EndoDB, a web-accessible collection of expert curated, quality assured and pre-analyzed data collected from 360 datasets comprising a total of 4741 bulk and 5847 single cell endothelial transcriptomes from six different organisms. Unlike other added-value databases, EndoDB allows to easily retrieve and explore data of specific studies, determine under which conditions genes and pathways of interest are deregulated and assess reprogramming of metabolism via principal component analysis, differential gene expression analysis, gene set enrichment analysis, heatmaps and metabolic and transcription factor analysis, while single cell data are visualized as gene expression color-coded t-SNE plots. Plots and tables in EndoDB are customizable, downloadable and interactive. EndoDB is freely available at https://vibcancer.be/software-tools/endodb, and will be updated to include new studies.