2020
DOI: 10.1016/j.bbrc.2020.03.121
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Multi-omics integrative analysis to access role of coiled-coil domain-containing 80 in lipid metabolism

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Cited by 10 publications
(4 citation statements)
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“…In another study, it was also mentioned that CCDC80 may be involved in energy and insulin metabolism in vivo, which is of great value for the prediction, diagnosis, and treatment strategy selection of gestational diabetes [21], and it was also mentioned that CCDC80 de ciency increases plasma and liver cholesterol levels in mice, leading to a greater susceptibility to hypercholesterolemia [22] and that the adipokine CCDC80 could be a predictive target for atherosclerosis in patients with in ammatory bowel disease [23]. In addition, the knockdown of CCDC80 in mouse models was found to reduce PPAR signaling processes and fatty acid degradation, leading to decreased levels of arachidonic and -linolenic acid metabolism [24]and promoting fat accumulation. CCDC80 expression seems to be closely related to PC, and in a recent study it was mentioned that ectopic expression of CCDC80 in mouse models was found to inhibit the epithelial-to-mesenchymal transition (EMT) process in pancreatic tumor cells, and inhibition of CCD80 invasion improved overall survival in a mouse model of PC [25], but this nding has not been con rmed in human-related studies.…”
Section: Discussionmentioning
confidence: 99%
“…In another study, it was also mentioned that CCDC80 may be involved in energy and insulin metabolism in vivo, which is of great value for the prediction, diagnosis, and treatment strategy selection of gestational diabetes [21], and it was also mentioned that CCDC80 de ciency increases plasma and liver cholesterol levels in mice, leading to a greater susceptibility to hypercholesterolemia [22] and that the adipokine CCDC80 could be a predictive target for atherosclerosis in patients with in ammatory bowel disease [23]. In addition, the knockdown of CCDC80 in mouse models was found to reduce PPAR signaling processes and fatty acid degradation, leading to decreased levels of arachidonic and -linolenic acid metabolism [24]and promoting fat accumulation. CCDC80 expression seems to be closely related to PC, and in a recent study it was mentioned that ectopic expression of CCDC80 in mouse models was found to inhibit the epithelial-to-mesenchymal transition (EMT) process in pancreatic tumor cells, and inhibition of CCD80 invasion improved overall survival in a mouse model of PC [25], but this nding has not been con rmed in human-related studies.…”
Section: Discussionmentioning
confidence: 99%
“…The lipids establishing a high number of correlations were predominantly glycerolphospholipids (125 correlations), followed by glycerolipids (11), bile acids (11); sphingolipids (9); sulfonolipids (7); amino acids and derivatives (2), and sterol lipids (1). Among the genes found upregulated in L+P, those more specifically involved in lipid metabolism and glucose homeostasis were Apolipoprotein E (APOE), Caveolae Associated Protein 1 (CAVIN1), Coiled-Coil Recently, a multi-omics analysis in mice elucidated the role of CCDC80 in regulating arachidonic acid and α-linolenic acid metabolism [47]. At the same time, elongases and desaturases (SCD and ELOVL5) are essential players in fatty acid elongation and desaturation, also regulating fatty acid functions and metabolic fates [48].…”
Section: Plos Onementioning
confidence: 99%
“…The CCDC80 (Coiled-Coil Domain Containing 80) was shown as a central core of the network predicted by STRING, and showed a decrease of its expression at mRNA level in response to the presence of the G allele of the rs516857374A>G. Recently, Li et al [75] showed that CCDC80-knockout could down-regulate PPAR signaling and fatty acid degradation. Furthermore, we identified that the G allele of the rs516857374A>G creates binding sites to a total of 30 genes.…”
Section: A Bta-mir-193a-2-snp May Influence γ-Linolenic Acid and ω6/ω3 Ratio Profilesmentioning
confidence: 99%