{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Jiang ZZ"],"funding":["National Key R&amp;D Program of China","Guangdong Basic and Applied Basic Research Foundation","National Natural Science Foundation of China","Guangdong Science and Technology Department"],"pagination":["2052418"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8928819"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["11(1)"],"pubmed_abstract":["Neutrophils constitute a major component in human hepatocellular carcinoma (HCC) and can facilitate disease progression via poorly understood mechanisms. Here, we show that neutrophil extracellular traps (NETs) formation was increased in human HCC tumor tissues than in paired non-tumor liver tissues. Mechanism study revealed that tumor-induced metabolic switch toward glycolysis and pentose phosphate pathway in tumor infiltrating neutrophils promoted NETs formation in a reactive oxygen species dependent-manner. NETs subsequently induced the migration of cancer cells and down-regulation of tight junction molecules on adjacent endothelial cells, thus facilitating tumor intravasation and metastasis. Accordingly, NETs depletion could inhibit tumor metastasis in mice <i>in vivo</i>, and the infi"],"journal":["Oncoimmunology"],"pubmed_title":["Neutrophil extracellular traps induce tumor metastasis through dual effects on cancer and endothelial cells."],"pmcid":["PMC8928819"],"funding_grant_id":["2020A1515111000","82071743","81730044","91842308","2020B1212060031","2021YFC2300601"],"pubmed_authors":["Peng ZP","Huang YF","Guo HF","Zhou MM","Ning WR","Zheng L","Jiang D","Jiang ZZ","Liu XC","Wu Y"],"additional_accession":[]},"is_claimable":false,"name":"Neutrophil extracellular traps induce tumor metastasis through dual effects on cancer and endothelial cells.","description":"Neutrophils constitute a major component in human hepatocellular carcinoma (HCC) and can facilitate disease progression via poorly understood mechanisms. Here, we show that neutrophil extracellular traps (NETs) formation was increased in human HCC tumor tissues than in paired non-tumor liver tissues. Mechanism study revealed that tumor-induced metabolic switch toward glycolysis and pentose phosphate pathway in tumor infiltrating neutrophils promoted NETs formation in a reactive oxygen species dependent-manner. NETs subsequently induced the migration of cancer cells and down-regulation of tight junction molecules on adjacent endothelial cells, thus facilitating tumor intravasation and metastasis. Accordingly, NETs depletion could inhibit tumor metastasis in mice <i>in vivo</i>, and the infi","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022","modification":"2025-04-05T13:25:36.011Z","creation":"2025-04-05T13:25:36.011Z"},"accession":"S-EPMC8928819","cross_references":{"pubmed":["35309732"],"doi":["10.1080/2162402X.2022.2052418"]}}