2020
DOI: 10.1016/j.jff.2019.103755
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Japonicone V, a sesquiterpene lactone derivative from the flowers of Inula japonica, inhibits hepatitis E virus replication by targeting virus-associated autophagy

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Cited by 5 publications
(5 citation statements)
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“…Furthermore, HEV infection had an inhibitory effect on the PI3K/AKT and mTOR signaling pathways; however, japonicone V therapy was able to counteract this effect in some cases. Following the findings (Zhao et al, 2020), it was discovered that inhibition of the AKT, PI3K, and mTOR pathways was effective in suppressing HEV reproduction by targeting virus-associated autophagy (Shen et al, 2016). This was accomplished, at least in part, by targeting the AKT, PI3K, and mTOR pathways, according to the findings (Zhao et al, 2020).…”
Section: Inula Japonicamentioning
confidence: 98%
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“…Furthermore, HEV infection had an inhibitory effect on the PI3K/AKT and mTOR signaling pathways; however, japonicone V therapy was able to counteract this effect in some cases. Following the findings (Zhao et al, 2020), it was discovered that inhibition of the AKT, PI3K, and mTOR pathways was effective in suppressing HEV reproduction by targeting virus-associated autophagy (Shen et al, 2016). This was accomplished, at least in part, by targeting the AKT, PI3K, and mTOR pathways, according to the findings (Zhao et al, 2020).…”
Section: Inula Japonicamentioning
confidence: 98%
“…Following the findings (Zhao et al, 2020), it was discovered that inhibition of the AKT, PI3K, and mTOR pathways was effective in suppressing HEV reproduction by targeting virus-associated autophagy (Shen et al, 2016). This was accomplished, at least in part, by targeting the AKT, PI3K, and mTOR pathways, according to the findings (Zhao et al, 2020).…”
Section: Inula Japonicamentioning
confidence: 98%
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“…Further, p62, an autophagosomal adaptor [412], displays a slightly elevated half-life in HEV-infected cells (Figure 24C). HEV-mediated effects on (auto-)lysosomal degradation could therefore also affect GBP1 co-degradation, as it is present on structures targeted for destruction [197,413]. In essence, this cross-talk of GBP1, HEV and the lysosomal system is of central interest for this study.…”
Section: Discussionmentioning
confidence: 99%