Neutrophil extracellular traps regulate LDHA expression to promote colorectal cancer liver metastasis

Metastasis is the most common cause of colorectal cancer (CRC)-related death. Neutrophil extracellular traps (NETs) promote tumor progression and distant metastasis. This study aimed to explore the role of NETs in CRC liver metastasis. Through analysis of publicly available single-cell transcriptome sequencing databases, in vitro experiments and nude mouse liver xenograft model experiments, we revealed that NETs promote CRC metastatic progression. Using scRNA-Seq technology, we showed that NETs marker expression was higher in metastatic lesions than in primary tumors. NET marker expression was high in colorectal cancer tissues and correlated with advanced tumor pathological grade. In addition, treatment with NETs enhanced the proliferation, migration and invasion of CRC cells in vitro by inducing EMT, as indicated by downregulation of E-cadherin and upregulation of N-cadherin and Vimentin. Cell-cell communication analysis revealed that NETs are related to the PI3K/AKT pathway and regulate the expression of LDHA, a key enzyme in glucose metabolism. In vitro, treatment with NETs promoted LDHA production and cell invasion and migration in CRC, while knockdown of LDHA suppressed EMT. Further, inhibition of LDHA expression or NET formation effectively inhibited NET-induced liver metastasis. In summary, this study elucidates the mechanism by which NETs regulate LDHA expression to promote CRC liver metastasis.

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Publication Details

Journal
Journal of Translational Medicine
Published
2025-11-03
DOI
https://doi.org/10.1186/s12967-025-07174-y
Citations
2
Primary Topic
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Type
article
Field-Weighted Citation Impact
1.59
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article

Neutrophil extracellular traps regulate LDHA expression to promote colorectal cancer liver metastasis

Congxue Hu, Jie Zheng, Sajid Khan, Tianming Jiang et al.
2 citations
Journal of Translational Medicine
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
1.59
article

Neutrophil extracellular traps regulate LDHA expression to promote colorectal cancer liver metastasis

Congxue Hu, Jie Zheng, Sajid Khan, Tianming Jiang, Qun Han, Xiaodong Li, Xinyu Zhang, Boshi Sun, Nana Li, Hao Yang, Shifeng Yang, Yanmei Yang
article en
2 citations

Abstract

Metastasis is the most common cause of colorectal cancer (CRC)-related death. Neutrophil extracellular traps (NETs) promote tumor progression and distant metastasis. This study aimed to explore the role of NETs in CRC liver metastasis. Through analysis of publicly available single-cell transcriptome sequencing databases, in vitro experiments and nude mouse liver xenograft model experiments, we revealed that NETs promote CRC metastatic progression. Using scRNA-Seq technology, we showed that NETs marker expression was higher in metastatic lesions than in primary tumors. NET marker expression was high in colorectal cancer tissues and correlated with advanced tumor pathological grade. In addition, treatment with NETs enhanced the proliferation, migration and invasion of CRC cells in vitro by inducing EMT, as indicated by downregulation of E-cadherin and upregulation of N-cadherin and Vimentin. Cell-cell communication analysis revealed that NETs are related to the PI3K/AKT pathway and regulate the expression of LDHA, a key enzyme in glucose metabolism. In vitro, treatment with NETs promoted LDHA production and cell invasion and migration in CRC, while knockdown of LDHA suppressed EMT. Further, inhibition of LDHA expression or NET formation effectively inhibited NET-induced liver metastasis. In summary, this study elucidates the mechanism by which NETs regulate LDHA expression to promote CRC liver metastasis.

Journal of Translational MedicineVol. 23(1)
Ministry of Education of the People's Republic of China (CN), Harbin Medical University (CN), Yale University (US), Third Affiliated Hospital of Harbin Medical University (CN), Second Affiliated Hospital of Harbin Medical University (CN), Ministry of Education (KN)
Openalex Percentile: Top 14%
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
1.59
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