Review
Copyright ©The Author(s) 2019.
World J Gastroenterol. Aug 14, 2019; 25(30): 4074-4091
Published online Aug 14, 2019. doi: 10.3748/wjg.v25.i30.4074
Table 1 Expression of hepatocyte nuclear factor 4alpha and variants in various disease states
Disease stateHNF4α expressionOrganismModelRef.
Development
Hypertriglyceridemia (preterm infants, children)Decreased, P1 promoter methylationHuman-[8,9]
Intrauterine growth restrictionDecreased, hypermethylated promoterHuman-[73]
High fat diet (in utero)IncreasedMouseHFD[87]
Metformin exposure (in utero)Increased, hypomethylated promoterMouseMetformin[74]
Liver
Acute phase responseDecreased activityMouseInjury[15]
Inflammation (IL-1β)DecreasedHuman, mouseHepatoma cells[14]
TNFα-induced hepatotoxicityDecreasedHuman, MouseHepatoma cells[88,89]
Alcoholic liver diseaseDecreasedMouseEthanol, MCD diets[17,89]
α1-antitrypsinDecreasedMouseHuman ATZ[90]
FibrosisDecreasedHumanHepatocytes[24]
CirrhosisDecreasedHuman, ratDEN[41,91]
Hepatocellular carcinomaP2 increased, P1 decreasedHuman, ratDEN[32,41,59]
Decreased, expressed in metastases, increased P1:P2Human, mouse, ratHCC cells, DEN[13,31,33,40,41,59,92]
Hepatitis B virusDecreasedHumanHepatoma cells[46,47]
Hepatitis C virusIncreasedHumanHepatoma cells[93,94]
DecreasedHuman, mouseHepatocytes, hepatoma cells, HCV+ HCC[35,95]
Hepatitis E virusIncreased phosphorylation, cytoplasmic retentionHumanHepatoma cells[48]
Non-alcoholic steatohepatitisModestly increasedHuman-[21]
Decreased, cytoplasmic retentionMousedb/db or HFD[18,22]
Iron overloadDecreasedHuman, mouseHepatoma cells, iron rich diet[49]
Endocrine
Type 2 diabetesDecreased, P1 promoter hypermethylationHuman-[72]
Increased in livermouseHFD, steptozotocin[76]
Mature onset diabetes of the young (MODY)HNF4α variantsHuman-[66-69]
ObesityHNF4α variantHuman-[79]
Islet cell hypoxiaDecreasedmouseob/ob[96]
Intestine
Micrbiome colonizationDecreasedZebrafish-[52]
IBDDecreasedHuman, mouse-[56,57]
Crohn diseaseHNF4α variant, decreasedHuman-[55,56,98]
Ulcerative colitisHNF4α variantHuman-[53,54]
Colorectal carcinomaDecreased or cytoplasmic retention, altered P1:P2, expressed in metastasesHuman, mouseMutagen[59,99,100]
Intestinal type ampullary carcinomaIncreasedHuman-[10]
Upper GI
Gastric carcinomaIncreased, altered P1:P2HumanCarcinoma cells[59,62,78,102]
Barrett esophagus (intestinal metaplasia)IncreasedHuman, mouseExplant[63,64]
Stomach intestinal metaplasiaIncreasedHuman-[59]
Kidney
Renal cell carcinomaDecreased, expressed in metastases, increased P1:P2Human-[59,103,104]
Atypical fanconi syndromeHNF4α variantHuman-[66]
Lung
Mucinous adenocarcinomasIncreased in someHuman-[82,100]
Ovary
Ovarian mucionous neoplasmExpressedHuman-[81]
Heart
Cardiac fibrosisIncreasedMouseAngiotensin II[83]
Table 2 Effects of experimental perturbations of hepatocyte nuclear factor 4alpha
HNF4α manipulationOrganismModelEffectRef.
Development
Overexpression of α1DHumaniPSCsPromoted endoderm differentiation[105]
Liver
OverexpressionHumanMarrow-derived mesenchymal stem cellsEpithelioid changes, glycogen storage, albumin secretion[6]
RatDENSuppressed carcinogenesis, suppressed EMT, decreased fibrosis, restored hepatic function in cirrhosis[5,26,41]
Ratmst1/2 conditional mutantReduced liver size and HCC proliferative indices[31]
MouseHepatoma cell xenograftDecreased tumorigenesis and proliferation[39,40]
MouseAcute liver failureIncreased survival, urea production[86]
KnockdownHumanHepatocyte culture, HBV infectionIncreased hepcidin expression, impaired transcription and replication of HBV, transformation and tumorigenicity in mice[13,36,42,43,106]
Liver targeted knockdownMouse-Increased hepatocyte proliferation and promitogenic transcription[38]
Expression of α7 onlyMouse-Steatosis, downregulation of CAR[75]
Liver targeted knockoutMouseDENUpregulation of miR-194 and -192, reduced transcriptional response to extracellular matrix rigidity, increased hepatocyte proliferation, HCC risk, steatosis[20,24,107,108]
Intestine
OverexpressionMouse, ratEmbryonal carcinoma cells, co-cultureDifferentiation to polarized epithelium, tight junction proteins[109,110]
Exon swapping, P1 or P2 onlyMouseDSSAltered enterocyte migration, ion transport, barrier function, susceptibility to DSS colitis and associated cancer[2]
Intestine targeted knockoutMouseDSSTranscription profiles similar to IBD, altered embyonic development, Paneth cell alterations, susceptibility to colitis[50,56,111,112]
Intestine targeted knockout of P1 and P2Mouse-Spontaneous intestinal inflammation[57]
Dominant negative expressionMouse, HumanEnterocytesDecreased expression of apolipoprotein A[113]
Upper GI
Esophagus overexpressionMouseEsophageal explantsInduced partial columnar cell phenotype[63]
Stomach overexpressionHumanGastric carcinoma cellsResistance to multiple chemotherapeutics[102]
Stomach knockdownHumanGastric carcinoma cellsIncreased susceptibility to chemotherapeutics[102]
Stomach targeted knockoutMouse-Reduced chief cell size, epithelial proliferation and migration[61]
Endocrine
HNF4α7 only expressionMouse-Dyslipidemia, mild steatosis[75]
HNF4α1 only expressionMouse-Impaired glucose tolerance, hyperinsulinemia[75]
Knockout in pancreatic beta cellsMouse-Reduced glucose stimulated insulin secretin, similar to MODY[65,70,71]
Overexpression in pancreatic beta cellsHumanislet cellsInduced cell cycle entry without expansion[114]