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Copyright ©The Author(s) 2016.
World J Virol. Nov 12, 2016; 5(4): 144-154
Published online Nov 12, 2016. doi: 10.5501/wjv.v5.i4.144
Table 1 Wnt/β-catenin molecular manipulations by human Herpesviridae
VirusPathway componentStabilization, activation or inhibition of pathway componentOutcomeRef.
Alphaherpesvirinae
HSV-1β-cateninStabilizedβ-catenin stabilized, increased transcriptional activity of β-catenin[35]
AxinStabilizedReduced host cell apoptosis[37,38]
GSK-3StabilizedPhosphorylation of APP[39]
Betaherpesvirinae
HCMVβ-cateninInhibitedβ-catenin degradation, decrease in β-catenin transcriptional targets[41]
AxinStabilizedTNKS PARsylation activity inhibited resulting in β-catenin degradation[50]
ROR2ActivatedRepression of β-catenin TCF/LEF-1 transcriptional activity[42]
GSK-3StabilizedStabilization of pAP and promotion of HCMV replication[52,53]
Gammaherpesvirinae
EBVβ-cateninStabilizedAccumulation of β-catenin in type III latency[59]
GSK-3InhibitedLMP2A activation of Akt inactivates GSK-3 resulting in β-catenin accumulation[60,61]
APCActivated/inhibited (conflicting results)LMP1 represses Siah-1 promoting β-catenin accumulation. LMP1 does not promote β-catenin stabilization[63,64]
KSHVβ-cateninStabilized/inhibited (dependent on viral stage?)Increased transcriptional activity, induction of viral latency/inhibition of LANA mediated transactivation of β-catenin[66,76,77]
GSK-3InhibitedLANA promotes nuclear accumulation of GSK-3[67,70]