Tumor immunity is related to 18 F-FDG uptake in thymic epithelial tumor

Cancer Med. 2021 Sep;10(18):6317-6326. doi: 10.1002/cam4.4176. Epub 2021 Aug 7.

Abstract

Background: 2-deoxy-2-[fluorine-18] fluoro-d-glucose (18 F-FDG) positron emission tomography (18 F-FDG-PET) is a convenient modality to assess the metabolic activity within tumor cells. However, there is no consensus regarding the relationship between 18 F-FDG uptake and the immune environment in thymic epithelial tumors (TETs). We conducted a clinicopathological study to elucidate the relationship between 18 F-FDG uptake and programmed death ligands 1 and 2 (PD-L1/PD-L2) expression in patients with TETs.

Methods: A total of 108 patients with histologically confirmed TETs classified as thymomas or thymic carcinomas who underwent surgical resection or biopsy or needle biopsy and 18 F-FDG PET before any treatment between August 2007 and March 2020 were enrolled in this study. Tumor specimens underwent immunohistochemical staining for PD-L1, PD-L2, GLUT1, HIF-1α, VEGFR2, VEGF-C, and β2 adrenergic receptor.

Results: High uptakes of SUVmax , SUVmean , MTV, and TLG were identified in 28 (25.9%), 61 (56.5%), 55 (50.9%), and 55 (50.9%) of 108 patients, respectively. High uptake of SUVmax significantly correlated with PS (performance status) of 1-2, thymic carcinoma, and advanced stage, and SUVmax on 18 F-FDG uptake displayed a close association with PD-L1 and PD-L2 expressions, but not with MTV and TLG. Our analysis revealed that SUVmax was identified as being significant relationship for positive PD-L1/PD-L2 expression. GLUT1, HIF-1α, and VEGFR2 were significantly associated with the expression of PD-L1/PD-L2 from the biological viewpoint.

Conclusion: 18 F-FDG accumulation was closely associated with the expression of PD-L1/PD-L2, which, in turn, was correlated with glucose metabolism and hypoxia. PD-L1/PD-L2 could affect the glucose metabolism and hypoxia in thymic tumor cells.

Keywords: 18F-FDG uptake; GLUT1; HIF-1α; PD-L1; PD-L2; immunohistochemistry; thymic epithelial tumor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • B7-H1 Antigen / analysis
  • B7-H1 Antigen / metabolism
  • Biopsy
  • Female
  • Fluorodeoxyglucose F18 / administration & dosage
  • Glucose Transporter Type 1 / analysis
  • Glucose Transporter Type 1 / metabolism
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / analysis
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Immunohistochemistry
  • Male
  • Middle Aged
  • Neoplasms, Glandular and Epithelial / diagnosis
  • Neoplasms, Glandular and Epithelial / immunology*
  • Neoplasms, Glandular and Epithelial / pathology
  • Neoplasms, Glandular and Epithelial / surgery
  • Positron-Emission Tomography / methods
  • Positron-Emission Tomography / statistics & numerical data
  • Programmed Cell Death 1 Ligand 2 Protein / analysis
  • Programmed Cell Death 1 Ligand 2 Protein / metabolism
  • Retrospective Studies
  • Thymectomy
  • Thymoma / diagnosis
  • Thymoma / immunology*
  • Thymoma / pathology
  • Thymoma / surgery
  • Thymus Gland / diagnostic imaging*
  • Thymus Gland / immunology
  • Thymus Gland / pathology
  • Thymus Gland / surgery
  • Thymus Neoplasms / diagnosis
  • Thymus Neoplasms / immunology*
  • Thymus Neoplasms / pathology
  • Thymus Neoplasms / surgery
  • Tumor Hypoxia / immunology
  • Warburg Effect, Oncologic

Substances

  • B7-H1 Antigen
  • CD274 protein, human
  • Glucose Transporter Type 1
  • HIF1A protein, human
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • PDCD1LG2 protein, human
  • Programmed Cell Death 1 Ligand 2 Protein
  • SLC2A1 protein, human
  • Fluorodeoxyglucose F18

Supplementary concepts

  • Thymic epithelial tumor