Journal of Advanced Research · 2020 · 77 citations · 37 references
MedicineImmunologyOncologyCancer ImmunologyTumor ImmunologyTumor MicroenvironmentCancer GenomicsDendritic Cell BiologyImmune Cell InfiltrationPancreatic CancerTumor Immune MicroenvironmentTumor-associated MacrophagesImmune Cell Infiltration DensityImmune Cell TranscriptomicsImmune Gene Expression SignaturesImmune Infiltration BiomarkersImmune Signature ProfilingPeripheral Immune Cell InfiltrationTumor Immune Cell InfiltrationTumor Immune Microenvironment Profiling
The details of the immunological microenvironment and its clinical implications for pancreatic cancer are still unclear. In this study, we obtained data from public databases, such as the Gene Expression Omnibus, the Cancer Genome Atlas Program, the International Cancer Genome Consortium Data Portal, the ArrayExpress Data Warehouse, and the cBioPortal for Cancer Genomics. We used these data to evaluate the pattern of immune cells infiltration in pancreatic ductal adenocarcinoma (PDAC) tissues. We observed that the levels of M0 macrophages and activated dendritic cells in tumor tissues were significantly higher than that in para-tumor tissues. M0 macrophages, gamma delta T cells and naive CD4 T cells were independent predictive factors of a poor outcome for PDAC patients. An immune score determined by M0 macrophages, gamma delta T cells and naive CD4 T cells could predict the survival of patients. The results of this study suggest that the infiltration of immune cells, such as M0 macrophages, may be a possible target for the treatment of PDAC. However, these findings need to be confirmed by additional studies.
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