PD-L1 neutrophils induced NETs in malignant ascites is a potential biomarker in HCC.

Xiaoyu Sun, Yaoqi Gui, Tai Yang, Lingbing Chen, Yi Zhang, Ling Yan, Weixian Chen, Bo Wang
Author Information
  1. Xiaoyu Sun: Department of Laboratory Medicine, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, China.
  2. Yaoqi Gui: Department of Laboratory Medicine, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, China.
  3. Tai Yang: Department of Laboratory Medicine, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, China.
  4. Lingbing Chen: Department of Laboratory Medicine, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, China.
  5. Yi Zhang: Department of Laboratory Medicine, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, China.
  6. Ling Yan: Department of Laboratory Medicine, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, China.
  7. Weixian Chen: Department of Laboratory Medicine, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, China.
  8. Bo Wang: Department of Laboratory Medicine, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, China. wang_bo@cqmu.edu.cn.

Abstract

BACKGROUND: Since differentiating malignant ascites from benign ascites has always been a clinical difficult, recognition of novel biomarkers in malignant ascites of hepatocellular carcinoma (HCC) patients could be helpful for establishing a diagnosis for HCC patients with ascitic fluids.
METHODS: Thirty-five HCC patients with malignant ascites and chronic liver diseases patients with benign ascites were enrolled. Serum and ascites specimens were collected to determine TAN subpopulations and NETs concentration. Then, the correlation between ascitic NETs levels and clinical features were analyzed, and ROC curves were generated to evaluate the diagnostic value of NETs. For in vitro study, fresh neutrophils were employed to explore the underlying mechanism of TAN polarization and NETs formation using RNAseq analysis.
RESULTS: Significantly increased pro-tumor PD-L1 TANs and higher lactate levels were measured in HCC ascites. RNAseq data showed that lactate regulated genes expression involving PD-L1 expression and NETs formation, suggesting that ascitic lactate might be responsible for tumor progression in TME. Then, NETs-related markers including calprotectin, dsDNA, CitH3, MPO and MPO-DNA were found dramatically elevated in malignant ascites. Next, correlation analysis revealed that ascitic NETs levels positively correlated with LDH, a classic ascitic biochemical indicator. Furthermore, we identified the diagnostic values of NETs in discriminating malignant ascites from benign ascites.
CONCLUSIONS: Our findings highlighted that elevated ascitic NETs served as a biomarker in HCC patients with malignant ascites, which provided useful insights for both clinical and basic research for malignant ascites diagnosis and management.

Keywords

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Grants

  1. 82302011/National Natural Science Foundation of China
  2. 202417-45/Kuanren Talents Program of the second affiliated hospital of Chongqing Medical University
  3. No. cstc2018jcyjAX0745/Natural Science Foundation of Chongqing Municipality

MeSH Term

Humans
Carcinoma, Hepatocellular
Liver Neoplasms
Neutrophils
Ascites
Biomarkers, Tumor
Male
B7-H1 Antigen
Female
Middle Aged
Extracellular Traps
Aged

Chemicals

Biomarkers, Tumor
B7-H1 Antigen
CD274 protein, human

Word Cloud

Created with Highcharts 10.0.0ascitesNETsmalignantHCCasciticpatientsPD-L1benignclinicallevelslactatediagnosisTANcorrelationdiagnosticneutrophilsformationRNAseqanalysisexpressionelevatedbiomarkerBACKGROUND:SincedifferentiatingalwaysdifficultrecognitionnovelbiomarkershepatocellularcarcinomahelpfulestablishingfluidsMETHODS:Thirty-fivechronicliverdiseasesenrolledSerumspecimenscollecteddeterminesubpopulationsconcentrationfeaturesanalyzedROCcurvesgeneratedevaluatevaluevitrostudyfreshemployedexploreunderlyingmechanismpolarizationusingRESULTS:Significantlyincreasedpro-tumorTANshighermeasureddatashowedregulatedgenesinvolvingsuggestingmightresponsibletumorprogressionTMENETs-relatedmarkersincludingcalprotectindsDNACitH3MPOMPO-DNAfounddramaticallyNextrevealedpositivelycorrelatedLDHclassicbiochemicalindicatorFurthermoreidentifiedvaluesdiscriminatingCONCLUSIONS:findingshighlightedservedprovidedusefulinsightsbasicresearchmanagementinducedpotentialBiomarkerMalignantNeutrophilextracellulartraps

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