METTL3 |
Adenosine analogues |
NA |
Reduces RNA m6A |
[170] |
|
UZH1a |
AML |
Suppress proliferation and viability of tumor cells in vitro |
[171] |
|
UZH2 |
AML, prostate cancer |
More potent anti-proliferative effects in vitro |
[172] |
|
STM2457 |
AML |
Anti-leukemia efficacy in vitro and in vivo |
[173] |
FTO |
Rhein |
AML |
Anti-leukemia efficacyin vitro and in vivo |
[159] |
|
MA2 |
GBM |
reduces GBM stem cell proliferation in vitro and tumor progression in mic |
[160] |
|
CHTB |
NA |
Increases RNA m6A |
[161] |
|
N-CDPCB |
NA |
Increases RNA m6A |
[162] |
|
R-2HG |
AML, GBM |
Anti-leukemia efficacy in vitro and in vivo, suppresses GBM in viro, synergizes with chemotherapeutic drugs |
[86] |
|
FB23-2 |
AML |
Anti-leukemia efficacy in vitro and in vivo |
[163] |
|
CS1 and CS2 |
AML |
potent anti-leukemic efficacy in mouse models, sensitize leukemia cells to T-cell cytotoxicity, overcomes immune evasion |
[150] |
|
Dac5 |
Melanoma |
Promotes activation and effector state of T cell, improving anti-PD1 blockade effects |
[151] |
|
FB23-13a |
AML |
Stronger anti-leukemia efficacy in vitro and in vivo |
[164] |
|
18,097 |
Breast cancer |
restrain in vivo growth and lung colonization |
[165] |
|
FTO-43 |
GC, AML, GBM |
Potent anti-tumor effects in mouse model |
[166] |
|
Compound C6 |
Esophageal cancer |
Anti-tumor efficacy in vitro and in vivo |
[167] |
|
|
AML |
Anti-leukemia and improves anti-PD1 blockade efficacy |
[169] |
ALKBH5 |
ALK-04 |
Melanoma |
Improve anti-PD-1 therapy efficiency |
[140] |
|
Compound 1 and 2 |
AML |
Anti-proliferative effects in specific AML cell lines |
[174] |
IGF2BP1 |
BTYNB |
Ovarian cancer |
Anti-tumor efficacy in vitro and in vivo |
[175] |