Published online Sep 20, 2022. doi: 10.5662/wjm.v12.i5.428
Peer-review started: December 13, 2021
First decision: March 24, 2022
Revised: April 1, 2022
Accepted: July 24, 2022
Article in press: July 24, 2022
Published online: September 20, 2022
Processing time: 277 Days and 4.2 Hours
Interleukin (IL)-6 is a proinflammatory cytokine that is involved in immunity, inflammation, angiogenesis, neural development and reproduction. The tumor microenvironment containing tumor cells, tumor-infiltrating immune cells and fibroblast stromal cells releases IL-6. IL-6 acts on the Janus kinase and signal transducer and activator of transcription factor pathway. These pathways release or associate with proteins that are responsible for major cellular functions.
This systematic review was motivated by a number of research studies that investigated the association between IL-6 and glioma.
In this systematic-review, case-control studies investigating the role of IL-6 with glioma development and progression have been discussed to review the utility of IL-6 as a biomarker.
Preferred Reporting Items for Systematic Reviews and Meta-analysis (PRISMA) guidelines were applied to filter the relevant studies based on inclusion and exclusion criteria. We used a combination of keywords and Reference Citation Analysis (RCA) tool to search for potential studies and performed data extraction from selected studies.
Five case–control studies were included for full evaluation. Most studies found a significantly higher level of IL-6 in cases as compared to controls although a study with contradictory results and a study with no difference in IL-6 level was also observed. Il-6 level varies with glioma stage, and some studies have reported lower levels in high-stage of cancer, whereas others have reported higher levels of IL-6 in early-stage glioma. Age at the time of diagnosis of glioma and IL-6 level could also have a significant relationship with glioma.
IL-6 could be a potential biomarker for the diagnosis and prognosis of glioma as it was increased twofold in cases of glioma as compared to controls.
Immunotherapy based treatment can be implemented by trigging IL-6 protein associated pathways and re-sensitizing the immune response to inhibit tumor growth and enhance survival rate.