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- W4313373589 abstract "Abstract Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal forms of cancer as the overall five-year survival rate was less than 5%. More than 90% of PDAC patients harbor Kras mutation, but only mutant Kras is insufficient to give rise to PDAC. Inflammation is essential to cooperate with mutant Kras for the initiation of pancreatic precancerous lesion, and attracted M1-polarized macrophages-induced inflammation are known to contribute to the process. Among TRIM family proteins, TRIM37 is the only protein containing MATH domain that endows it being able to interact with proteins containing TRAF domain, indicating its possible role in regulating pattern recognition receptor-, TNFR- and cytokine-mediated signaling pathways. We have observed that, when TRIM37 was knocked-down, macrophage cytokines production, such as IL-1β, IFN-β, IL-12, TNF-a, IL-6 and CCL-2 in response to LPS was reduced, and the regulation was both epigenetically and non-epigenetically. Interestingly, pro-inflammatory cytokines also upregulated TRIM37 expression in macrophages. Thus our data implicated that upregulated TRIM37 that positively regulate macrophage cytokine production might contribute to the initiation of PDAC. However, when macrophages were co-cultured with pancreatic cancer cells, the expression level of TRIM37 in macrophages were downregulated, this led to the loss of its ability in maintaining macrophages in a stable M1 phenotype, and instead, skewing the macrophages into a M2 phenotype, which promotes cancer progression. In conclusion, our data demonstrate that during pancreatic cancer development, the expression of TRIM37 in macrophages are differential regulated to favor cancer development and progression." @default.
- W4313373589 created "2023-01-06" @default.
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- W4313373589 date "2020-05-01" @default.
- W4313373589 modified "2023-09-27" @default.
- W4313373589 title "Dynamic regulation of TRIM37 expression in macrophages facilitates pancreatic cancer development" @default.
- W4313373589 doi "https://doi.org/10.4049/jimmunol.204.supp.164.17" @default.
- W4313373589 hasPublicationYear "2020" @default.
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