Dataset Information


Lectin-type oxidized LDL receptor 1 defines population of polymorphonuclear myeloid-derived suppressor cells in cancer patients

ABSTRACT: Polymorphonuclear myeloid-derived suppressor cells (PMN-MDSC) are important regulators of immune responses and promoters of tumor progression in cancer1,2. The heterogeneity of these cells as well as their distinction from neutrophils hampers the progress in understanding of the biology and clinical significance of these cells. PMN-MDSC had a distinct gene signature from neutrophils isolated from the same patients with most prominent changes in genes associated with endoplasmic reticulum (ER) stress response. Surprisingly, low-density lipoprotein (LDL) was one of the most enriched gene regulators and oxidized LDL receptor 1 (OLR1) was one of the most overexpressed genes in PMN-MDSC. Lectin-type oxidized LDL receptor 1 (LOX-1) encoded by OLR1 was expressed in only 0.7% of neutrophils in peripheral blood of healthy donors, whereas 5-15% of neutrophils in cancer patients and 15-50% of neutrophils in tumor tissues were LOX-1+. In contrast to their LOX-1- counterparts, LOX-1+ neutrophils had gene signature, biochemical and functional characteristics of PMN-MDSC. Induction of ER stress in neutrophils from healthy donors up-regulated LOX-1 expression and converted these cells to suppressive PMN-MDSC. Thus, PMN-MDSC have distinct gene signature and LOX-1 can define this population of cells, which may provide new insight to the biology and clinical evaluation of these cells. Examination of LOX1+/LOX1- and PMN/MDSC cells in cancer patient samples

ORGANISM(S): Homo sapiens  

SUBMITTER: T Condamine   D Gabrilovich  Priyankara J Wickramasinghe 

PROVIDER: E-GEOD-79404 | ArrayExpress | 2016-07-22



Dataset's files

Action DRS Other
E-GEOD-79404.idf.txt Idf Processed
E-GEOD-79404.sdrf.txt Txt
Items per page:
1 - 4 of 4

Similar Datasets

2016-01-01 | S-EPMC5391495 | BioStudies
2015-01-01 | S-EPMC4436670 | BioStudies
2019-05-09 | GSE126885 | GEO
2020-01-01 | S-EPMC7455061 | BioStudies
2018-01-01 | S-EPMC6085951 | BioStudies
1000-01-01 | S-EPMC2322963 | BioStudies
2020-01-01 | S-EPMC7270107 | BioStudies
2017-01-01 | S-EPMC5343826 | BioStudies
2016-01-01 | S-EPMC4717858 | BioStudies
2020-05-19 | E-MTAB-8389 | BioStudies