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. 2022 May 7;15:51. doi: 10.1186/s13045-022-01262-y

Table 1.

Small molecules and/or agents for activation of autophagy in the context of AML treatment

Agents Known for Mechanism Outcome/effects Study model Ref
Vitamin D Inhibition of miR-17-5p and induction of Beclin-1, Inhibition of cell proliferation HL-60, AML patients sample [149]
Dendrogenin A A mammalian cholesterol metabolite LXRβ-dependent sensitization of AML cells to Ara-C in vitro and in vivo Potentiation of Ara-C cytotoxicity HL-60, KG1, MV4-11, AML patients samples, AML xenograft in mice [185]
Inhibition of phosphorylation of Akt and JNK to maximize the idarubicin induced DNA damage and lethal autophagy Potentiation of Idarubicin-induced cell death KG1α, KG1, MOLM14, OCI-AML3, AML patients samples, xenograft in mice [184]
LXRβ-, Nur77-, and NOR1-dependent induction of lethal autophagy Anti-leukemic effect KG1, HL-60, AML patients samples, AML xenograft in mice [186]
Dihydroartemisinin Anti-malarial drug Inhibition of mTOR/p70S6k signaling and activation of AMPK leading to autophagy dependent ferroptosis Induction of ferroptosis, inhibition of cell/xenograft growth HL-60, KG1, THP-1, AML xenograft in mice [187]
AC-73 Specific inhibitor of CD147 Inhibition of ERK/STAT3 signaling and potentiation of ATO-induced autophagy Inhibition of cell proliferation U937, NB4, HL-60, MV4-11, AML patients samples [188]

LXRβ oxysterols receptor LXR-beta, Ara-C cytarabine, JNK c-Jun N-terminal kinase, Nur77 transcription factors NR4A1, NOR1 transcription factors NR4A3, CD147 cluster of differentiation 147, ATO arsenic trioxide