Inverse correlation between Interleukin-34 and gastric cancer, a potential biomarker for prognosis
| Field | Value | Language |
| dc.contributor.author | Liu, Qinghua | en |
| dc.contributor.author | Zhang, Ying | en |
| dc.contributor.author | Zhang, Jiwei | en |
| dc.contributor.author | Tao, Kun | en |
| dc.contributor.author | Hambly, Brett D | en |
| dc.contributor.author | Bao, Shisan | en |
| dc.date.accessioned | 2020-08-14 | |
| dc.date.available | 2020-08-14 | |
| dc.date.issued | 2020 | en |
| dc.identifier.uri | https://hdl.handle.net/2123/23073 | |
| dc.description.abstract | Gastric cancer (GC) is a malignancy with high morbidity/mortality, partly due to a lack of reliable biomarkers for early diagnosis. It is important to develop reliable biomarker(s) with specificity, sensitivity and convenience for early diagnosis. The role of tumour-associated macrophages (TAMs) and survival of GC patients are controversial. Macrophage colony stimulating factor (MCSF) regulates monocytes/macrophages. Elevated MCSF is correlated with invasion, metastasis and poor survival of tumour patients. IL-34, a ligand of the M-CSF receptor, acts as a “twin” to M-CSF, demonstrating overlapping and complimentary actions. IL-34 involvement in tumours is controversial, possibly due to the levels of M-CSF receptors. While the IL-34/M-CSF/M-CSFR axis is very important for regulating macrophage differentiation, the specific interplay between these cytokines, macrophages and tumour development is unclear. | en |
| dc.language.iso | en | en |
| dc.rights | Other | |
| dc.subject | COVID-19 | en |
| dc.subject | Coronavirus | en |
| dc.title | Inverse correlation between Interleukin-34 and gastric cancer, a potential biomarker for prognosis | en |
| dc.type | Preprint | en |
| dc.identifier.doi | 10.21203/rs.3.rs-26741/v2 | |
| usyd.faculty | Faculty of Medicine and Health, Sydney Medical School | en |
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