hsa-miR-93 regulates MUCIN family gene expression via WNT/β-catenin pathway in intrahepatic stone disease

•Mucins family, miR-93 and wnt pathway play an important role in the pathogenesis of intrahepatic stone.•Mucin3/4/5ac/B levels were found increased in patients with intrahepatic bile duct stones, and miR-93 levels were decreased.•Beta-catenin and wnt4 levels were higher also in subjects with intrahe...

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Published inClinics and research in hepatology and gastroenterology Vol. 42; no. 5; pp. 453 - 461
Main Authors Ma, Hua, Li, Wenyi, Bi, Pinduan, Wang, Qiang, Li, Jian, Yang, Bin
Format Journal Article
LanguageEnglish
Published France Elsevier Masson SAS 01.10.2018
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ISSN2210-7401
2210-741X
2210-741X
DOI10.1016/j.clinre.2018.03.013

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Abstract •Mucins family, miR-93 and wnt pathway play an important role in the pathogenesis of intrahepatic stone.•Mucin3/4/5ac/B levels were found increased in patients with intrahepatic bile duct stones, and miR-93 levels were decreased.•Beta-catenin and wnt4 levels were higher also in subjects with intrahepatic bile duct stones.•Activition of wnt pathway up-regulated the expression of MUC4 and MUC5B, not MUC3 and MUC5ac.•miR-93 directly targeted TCF7 and repressed the activation of non-canonical, not canonical Wnt pathway.•miR-93 decreases the expression of MUC4/5ac/5B induced by wnt4. Mucin plays an essential role in the intrahepatic stone formation, but the mechanism of mucin regulation is unclear. To investigate the potential implication of miR-93 and WNT pathway in the regulation of intrahepatic bile duct mucin expression. Thirty patients with or without intrahepatic bile duct stones are involved; Reverse-transcription polymerase chain reaction was performed to evaluate the expression of MUC3, MUC4, MUC5B, MUC5AC mRNA and miR-93 levels. miR-NC or miR-93 mimics was transfected into intrahepatic biliary epithelial cells. Then mucins and Wnt pathway proteins were detected by the immunoblotting, and the target gene TCF7 were validated using the dual luciferase assay. β-catenin, wnt4, and mucins were an immunohistochemical stain of the intrahepatic biliary epithelial tissues. The expression levels of MUC3, MUC4, MUC5B, and MUC5AC in patients with intrahepatic bile duct stones are higher than control, as well as Wnt pathway proteins (especially β-catenin and wnt4). Mucins levels increased in wnt4, wnt5a or SB216763-treated HIBECs, and reduced by miR-93 mimics transfection. miR-93 directly targeted TCF7 and repressed Wnt pathway protein expression, which reversed the upregulation of mucin levels induced by wnt4 or wnt5a, but not SB216763. These results suggest a new potential mechanism in intrahepatic stones, regulating by miR-93/TCF7, non-canonical Wnt pathway, and mucins.
AbstractList •Mucins family, miR-93 and wnt pathway play an important role in the pathogenesis of intrahepatic stone.•Mucin3/4/5ac/B levels were found increased in patients with intrahepatic bile duct stones, and miR-93 levels were decreased.•Beta-catenin and wnt4 levels were higher also in subjects with intrahepatic bile duct stones.•Activition of wnt pathway up-regulated the expression of MUC4 and MUC5B, not MUC3 and MUC5ac.•miR-93 directly targeted TCF7 and repressed the activation of non-canonical, not canonical Wnt pathway.•miR-93 decreases the expression of MUC4/5ac/5B induced by wnt4. Mucin plays an essential role in the intrahepatic stone formation, but the mechanism of mucin regulation is unclear. To investigate the potential implication of miR-93 and WNT pathway in the regulation of intrahepatic bile duct mucin expression. Thirty patients with or without intrahepatic bile duct stones are involved; Reverse-transcription polymerase chain reaction was performed to evaluate the expression of MUC3, MUC4, MUC5B, MUC5AC mRNA and miR-93 levels. miR-NC or miR-93 mimics was transfected into intrahepatic biliary epithelial cells. Then mucins and Wnt pathway proteins were detected by the immunoblotting, and the target gene TCF7 were validated using the dual luciferase assay. β-catenin, wnt4, and mucins were an immunohistochemical stain of the intrahepatic biliary epithelial tissues. The expression levels of MUC3, MUC4, MUC5B, and MUC5AC in patients with intrahepatic bile duct stones are higher than control, as well as Wnt pathway proteins (especially β-catenin and wnt4). Mucins levels increased in wnt4, wnt5a or SB216763-treated HIBECs, and reduced by miR-93 mimics transfection. miR-93 directly targeted TCF7 and repressed Wnt pathway protein expression, which reversed the upregulation of mucin levels induced by wnt4 or wnt5a, but not SB216763. These results suggest a new potential mechanism in intrahepatic stones, regulating by miR-93/TCF7, non-canonical Wnt pathway, and mucins.
Mucin plays an essential role in the intrahepatic stone formation, but the mechanism of mucin regulation is unclear. To investigate the potential implication of miR-93 and WNT pathway in the regulation of intrahepatic bile duct mucin expression. Thirty patients with or without intrahepatic bile duct stones are involved; Reverse-transcription polymerase chain reaction was performed to evaluate the expression of MUC3, MUC4, MUC5B, MUC5AC mRNA and miR-93 levels. miR-NC or miR-93 mimics was transfected into intrahepatic biliary epithelial cells. Then mucins and Wnt pathway proteins were detected by the immunoblotting, and the target gene TCF7 were validated using the dual luciferase assay. β-catenin, wnt4, and mucins were an immunohistochemical stain of the intrahepatic biliary epithelial tissues. The expression levels of MUC3, MUC4, MUC5B, and MUC5AC in patients with intrahepatic bile duct stones are higher than control, as well as Wnt pathway proteins (especially β-catenin and wnt4). Mucins levels increased in wnt4, wnt5a or SB216763-treated HIBECs, and reduced by miR-93 mimics transfection. miR-93 directly targeted TCF7 and repressed Wnt pathway protein expression, which reversed the upregulation of mucin levels induced by wnt4 or wnt5a, but not SB216763. These results suggest a new potential mechanism in intrahepatic stones, regulating by miR-93/TCF7, non-canonical Wnt pathway, and mucins.
Mucin plays an essential role in the intrahepatic stone formation, but the mechanism of mucin regulation is unclear.BACKGROUNDMucin plays an essential role in the intrahepatic stone formation, but the mechanism of mucin regulation is unclear.To investigate the potential implication of miR-93 and WNT pathway in the regulation of intrahepatic bile duct mucin expression.OBJECTIVETo investigate the potential implication of miR-93 and WNT pathway in the regulation of intrahepatic bile duct mucin expression.Thirty patients with or without intrahepatic bile duct stones are involved; Reverse-transcription polymerase chain reaction was performed to evaluate the expression of MUC3, MUC4, MUC5B, MUC5AC mRNA and miR-93 levels. miR-NC or miR-93 mimics was transfected into intrahepatic biliary epithelial cells. Then mucins and Wnt pathway proteins were detected by the immunoblotting, and the target gene TCF7 were validated using the dual luciferase assay. β-catenin, wnt4, and mucins were an immunohistochemical stain of the intrahepatic biliary epithelial tissues.METHODSThirty patients with or without intrahepatic bile duct stones are involved; Reverse-transcription polymerase chain reaction was performed to evaluate the expression of MUC3, MUC4, MUC5B, MUC5AC mRNA and miR-93 levels. miR-NC or miR-93 mimics was transfected into intrahepatic biliary epithelial cells. Then mucins and Wnt pathway proteins were detected by the immunoblotting, and the target gene TCF7 were validated using the dual luciferase assay. β-catenin, wnt4, and mucins were an immunohistochemical stain of the intrahepatic biliary epithelial tissues.The expression levels of MUC3, MUC4, MUC5B, and MUC5AC in patients with intrahepatic bile duct stones are higher than control, as well as Wnt pathway proteins (especially β-catenin and wnt4). Mucins levels increased in wnt4, wnt5a or SB216763-treated HIBECs, and reduced by miR-93 mimics transfection. miR-93 directly targeted TCF7 and repressed Wnt pathway protein expression, which reversed the upregulation of mucin levels induced by wnt4 or wnt5a, but not SB216763.RESULTSThe expression levels of MUC3, MUC4, MUC5B, and MUC5AC in patients with intrahepatic bile duct stones are higher than control, as well as Wnt pathway proteins (especially β-catenin and wnt4). Mucins levels increased in wnt4, wnt5a or SB216763-treated HIBECs, and reduced by miR-93 mimics transfection. miR-93 directly targeted TCF7 and repressed Wnt pathway protein expression, which reversed the upregulation of mucin levels induced by wnt4 or wnt5a, but not SB216763.These results suggest a new potential mechanism in intrahepatic stones, regulating by miR-93/TCF7, non-canonical Wnt pathway, and mucins.CONCLUSIONThese results suggest a new potential mechanism in intrahepatic stones, regulating by miR-93/TCF7, non-canonical Wnt pathway, and mucins.
Author Bi, Pinduan
Wang, Qiang
Yang, Bin
Li, Wenyi
Ma, Hua
Li, Jian
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  email: allan11182@163.com
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/29705272$$D View this record in MEDLINE/PubMed
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Keywords Wnt pathways
Mucin
miR-93
Intrahepatic stones
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Snippet •Mucins family, miR-93 and wnt pathway play an important role in the pathogenesis of intrahepatic stone.•Mucin3/4/5ac/B levels were found increased in patients...
Mucin plays an essential role in the intrahepatic stone formation, but the mechanism of mucin regulation is unclear. To investigate the potential implication...
Mucin plays an essential role in the intrahepatic stone formation, but the mechanism of mucin regulation is unclear.BACKGROUNDMucin plays an essential role in...
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SubjectTerms Intrahepatic stones
miR-93
Mucin
Wnt pathways
Title hsa-miR-93 regulates MUCIN family gene expression via WNT/β-catenin pathway in intrahepatic stone disease
URI https://www.clinicalkey.com/#!/content/1-s2.0-S2210740118300731
https://www.ncbi.nlm.nih.gov/pubmed/29705272
https://www.proquest.com/docview/2032800835
Volume 42
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