Title : HMGB1 knockdown increases MM cell vulnerability by regulating autophagy and DNA damage repair.

Pub. Date : 2018 Aug 29

PMID : 30157958






5 Functional Relationships(s)
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Protein Name
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1 HMGB1 knockdown in MM cells enhanced the inhibitory effect of chemotherapy with dexamethasone (Dex) via apoptosis induction. Dexamethasone high mobility group box 1 Homo sapiens
2 HMGB1 knockdown in MM cells enhanced the inhibitory effect of chemotherapy with dexamethasone (Dex) via apoptosis induction. Dexamethasone high mobility group box 1 Homo sapiens
3 Furthermore, downregulation of HMGB1 activated the mTOR pathway, inhibited autophagy and increased DNA damage induced by Dex by modulating expression of related genes. Dexamethasone high mobility group box 1 Homo sapiens
4 CONCLUSIONS: Our research shows that HMGB1 participates in autophagy and DNA damage repair and that downregulation of HMGB1 enhances the sensitivity of MM cells to Dex, suggesting that HMGB1 may serve as a target for MM treatment. Dexamethasone high mobility group box 1 Homo sapiens
5 CONCLUSIONS: Our research shows that HMGB1 participates in autophagy and DNA damage repair and that downregulation of HMGB1 enhances the sensitivity of MM cells to Dex, suggesting that HMGB1 may serve as a target for MM treatment. Dexamethasone high mobility group box 1 Homo sapiens