High blood levels of soluble OX40 (CD134), an immune costimulatory molecule, indicate reduced survival in patients with advanced colorectal cancer.
Adult
Aged
Aged, 80 and over
Antigens, Tumor-Associated, Carbohydrate
/ blood
C-Reactive Protein
/ metabolism
Carcinoembryonic Antigen
/ blood
Colorectal Neoplasms
/ genetics
Female
Gene Expression Regulation, Neoplastic
Humans
Jurkat Cells
Male
Middle Aged
Neoplasm Staging
Organothiophosphorus Compounds
/ blood
Receptors, OX40
/ blood
Serum Albumin, Human
/ metabolism
Survival Analysis
Up-Regulation
Journal
Oncology reports
ISSN: 1791-2431
Titre abrégé: Oncol Rep
Pays: Greece
ID NLM: 9422756
Informations de publication
Date de publication:
Nov 2019
Nov 2019
Historique:
received:
13
03
2019
accepted:
12
07
2019
pubmed:
24
9
2019
medline:
28
2
2020
entrez:
24
9
2019
Statut:
ppublish
Résumé
The interaction between tumor necrosis factor receptor superfamily, member 4 (OX40) on T cells and the OX40 ligand (OX40L) on antigen‑presenting cells (APCs) is a pivotal step for T‑cell activation and the promotion of antitumor immunity. However, it is hypothesized that soluble OX40 (sOX40) in blood suppresses T‑cell activation by blocking the OX40/OX40L interaction. In the present study, the association between blood sOX40 levels and the clinical characteristics of advanced colorectal cancer (CRC) patients was investigated. Blood was collected from 22 patients with advanced CRC. Blood sOX40 levels were determined by enzyme‑linked immunosorbent assay (ELISA). Messenger RNA (mRNA) expression encoding OX40 or cytokines was analyzed by quantitative RT‑PCR. Blood sOX40 levels were positively correlated with the blood levels of carbohydrate antigen (CA) 19‑9, carcinoembryonic antigen (CEA), C‑reactive protein (CRP) and soluble programmed cell death ligand‑1 (PD‑L1) in patients but negatively correlated with the blood levels of albumin. Blood sOX40 levels were not correlated with the mRNA expression of interferon (IFN)‑gamma, interleukin (IL)‑6, IL‑10 and IL‑4 in the peripheral blood mononuclear cells (PBMCs) of the patients and were not correlated with the frequency of programmed cell death‑1 (PD‑1) expressing CD4+, CD8+ and CD56+ cells. Notably, according to both univariate and multivariate analyses, high blood sOX40 levels were significantly correlated with a reduced survival time in patients. Although activated Jurkat cells (a human T cell line) exhibited an upregulation of sOX40 production and OX40 mRNA expression, the OX40 mRNA expression of the PBMCs of patients was not correlated with blood sOX40 levels. High blood levels of sOX40 were correlated with a reduced survival time in patients with advanced CRC, possibly associated with the suppression of antitumor immunity by sOX40.
Identifiants
pubmed: 31545443
doi: 10.3892/or.2019.7304
doi:
Substances chimiques
Antigens, Tumor-Associated, Carbohydrate
0
Carcinoembryonic Antigen
0
Organothiophosphorus Compounds
0
Receptors, OX40
0
TNFRSF4 protein, human
0
carbohydrate antigen 199, human
0
C-Reactive Protein
9007-41-4
phosfolan
CHJ98J84AY
Serum Albumin, Human
ZIF514RVZR
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM