Methods for detection and eradication of myeloid leukemia stem cells
There are provided, inter alia, methods and compositions for diagnosis and treatment of acute myeloid leukemia (AML), secondary acute myeloid leukemia (sAML), and age-related diseases.
1. A method for treating acute myeloid leukemia in a subject in need thereof by modulation of acute myeloid leukemia stem cells, the method comprising administering to the subject an effective amount of a splicing modulator selected from a compound of Formula (I) or a pharmaceutically acceptable salt thereof; wherein the compound of Formula (I) is:
wherein:
X 1 is N, O, or CH 2 ;
X 2 is O or C(R 6 )(R 7 );
R 6 and R 7 are each independently hydrogen, halogen, substituted or unsubstituted alkyl, substituted or unsubstituted aryl, —OR 12 , —OC(O)R 12 , —OC(O)OR 12 , or —OC(O)NR 13 R 14 ;
R 1 is hydrogen, —C(O)R 8 , —OC(O)R 8 , —OC(O)OR 8 , or —NHC(O)NHR 8 ;
R 2 , R 3 , R 4 , and R 5 are each independently hydrogen, substituted or unsubstituted alkyl, —OR 9 , —OC(O)R 9 , —OC(O)OR 9 , or —OC(O)NR 10 R 11 ;
R 8 , R 9 , R 10 , R 11 , R 12 , R 13 and R 14 are each independently hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; and
R 15 is hydrogen, halogen, CF 3 , CCl 3 , CBr 3 , CI 3 , or substituted or unsubstituted alkyl;
wherein:
(i) when X 2 is O, then the chiral carbon at R 2 has (R) stereochemistry, and the chiral carbon at R 4 has (S) stereochemistry; or when X 2 is O, then the chiral carbon at R 2 has (S) stereochemistry, and the chiral carbon at R 4 has (R) stereochemistry;
(ii) when R 2 is attached to a chiral carbon having (S) stereochemistry, then R 4 is attached to a chiral carbon having (S) or (R) stereochemistry; and
(iii) when X 2 is C(R 6 )(R 7 ), then the chiral carbon at R 2 has (R) stereochemistry, and the chiral carbon at R 4 has (S) stereochemistry; or when X 2 is (R 6 )(R 7 ), then the chiral carbon at R 2 has (S) stereochemistry, and the chiral carbon at R 4 has (R) stereochemistry.
2. The method of claim 1 , wherein the compound of Formula (I) is:
wherein R 1 is hydrogen or acetyl; R 6 and R 7 are each independently hydrogen, halogen, or methyl; R 9 is hydrogen or C 1 -C 4 unsubstituted alkyl; and R 15 is hydrogen or C 1 -C 4 unsubstituted alkyl.
3. The method of claim 1 , wherein the compound of Formula (I) is:
4. The method of claim 1 , wherein the acute myeloid leukemia is secondary acute myeloid leukemia, refractory acute myeloid leukemia, or relapsed acute myeloid leukemia.
5. The method of claim 1 , further comprising
(i) obtaining a biological sample from the subject prior to administering the compound of Formula (I) or the pharmaceutically acceptable salt thereof;
(ii) detecting a protein expression level of 1 to 100 proteins encoded by an RNA by contacting the biological sample with a detection agent capable of binding the one or more proteins, thereby forming a detectable complex; wherein the 1 to 100 proteins are encoded by an RNA selected from a first set or RNA and/or a second set of RNA, wherein
(a) the first set of RNA comprises FXYD5-009, RPS3-023, RPS24-002, NAP1L1-018, TRGC2-001, CD44-012, ACTG1-014, S100A10-001, EIF3A-201, ACTG1-006, NRD1-005, ITGB2-201, PTPN6-003, TYROBP-002, ARPC1B-001, ANPEP-001, LMAN1-005, TAC3-010, C1orf228-020, CEP57-011, TWF2-001, ARRB2-003, PTK2B-202, C1orf228-011, DCP2-008, PPP1R18-003, RPL37P2-001, TMUB2-002, OAZ2-001, PTK2B-001, RP11-7707.1-001, XPC-007, SDR39U1-003, MACF1-014, SWSAP1-001, MGA-002, FHL3-002, ZC3H15-005, GPSM3-001, RBM28-003, LPIN2-002, PXN-002, WASF2-001, EIF4A1-001, RN7SL182P-201, SSBP4-008, PRR12-001, GOLGA4-004, ANKRD11-011, and C1orf228-005;
(b) the second set of RNA comprises TMEM106C-007, RABL5-007, EIF4G2-022, HNRNPA1P7-001, RPLP0-008, CANX-005, TMEM106C-020, CTNNAL1-003, NPM1P27-001, NCAPH2-016, SRRM1-017, FAM129C-007, HMGB1-012, RC3H1-201, UGT3A2-001, WIPF3-002, RP11-315A17.1-001, ING3-006, ING3-005, CA1-009, IGHV5-78-001, CAST-038, CDH1-001, ING3-002, CXADR-001, HMHB1-001, AC015987.2-201, TYMS-002, ZFP36L2-001, CAST-039, VPREB1-002, EWSR1-019, FAM134A-004, AC096579.7-001, RNU1-78P-201, SELENBP1-001, HBB-001, EBF1-001, CLC-001, RGS2-001, UCA1-001, FTH1-002, AHSP-001, SNORA22-201, TMBIM6-006, NPY-001, RGS1-001, BLOC1S1-001, VPREB3-001, and RPL14-003; and
(iii) detecting and quantitating the detectable complex to detect the protein expression level.
6. The method of claim 5 , further comprising comparing the protein expression level to a subject that does not have acute myeloid leukemia.
7. The method of claim 6 , wherein the acute myeloid leukemia is responsive to treatment with the compound of Formula (I) if the protein expression level of the first set of RNA is higher than in the subject that does not have acute myeloid leukemia; or wherein the acute myeloid leukemia is responsive to treatment with the compound of Formula (I) if the protein expression level of the second set of RNA is lower than in the subject that does not have acute myeloid leukemia.
8. The method of claim 5 , wherein the 1 to 100 proteins is PTK2B, CD44, or a combination thereof.
9. The method of claim 5 , comprising detecting the expression level of 5 to 100 proteins encoded by the RNA selected from the first set or RNA and/or the second set of RNA.
10. The method of claim 9 , comprising detecting the expression level of 50 to 100 proteins encoded by the RNA selected from the first set or RNA and/or the second set of RNA.
11. The method of claim 1 , further comprising
(i) obtaining a biological sample from the subject prior to administering the compound of Formula (I) or the pharmaceutically acceptable salt thereof;
(ii) detecting an expression level in 1 to 100 RNA by contacting the biological sample with one or more probes capable of hybridizing the 1 to 100 RNA, thereby forming a hybridized complex; wherein the one or more RNA are selected from a first set of RNA and/or a second set of RNA, wherein:
(a) the first set of RNA comprises FXYD5-009, RPS3-023, RPS24-002, NAP1L1-018, TRGC2-001, CD44-012, ACTG1-014, S100A10-001, EIF3A-201, ACTG1-006, NRD1-005, ITGB2-201, PTPN6-003, TYROBP-002, ARPC1B-001, ANPEP-001, LMAN1-005, TAC3-010, C1orf228-020, CEP57-011, TWF2-001, ARRB2-003, PTK2B-202, C1orf228-011, DCP2-008, PPP1R18-003, RPL37P2-001, TMUB2-002, OAZ2-001, PTK2B-001, RP11-7707.1-001, XPC-007, SDR39U1-003, MACF1-014, SWSAP1-001, MGA-002, FHL3-002, ZC3H15-005, GPSM3-001, RBM28-003, LPIN2-002, PXN-002, WASF2-001, EIF4A1-001, RN7SL182P-201, SSBP4-008, PRR12-001, GOLGA4-004, ANKRD11-011, and C1orf228-005,
(b) the second set of RNA comprises TMEM106C-007, RABL5-007, EIF4G2-022, HNRNPA1P7-001, RPLP0-008, CANX-005, TMEM106C-020, CTNNAL1-003, NPM1P27-001, NCAPH2-016, SRRM1-017, FAM129C-007, HMGB1-012, RC3H1-201, UGT3A2-001, WIPF3-002, RP11-315A17.1-001, ING3-006, ING3-005, CA1-009, IGHV5-78-001, CAST-038, CDH1-001, ING3-002, CXADR-001, HMHB1-001, AC015987.2-201, TYMS-002, ZFP36L2-001, CAST-039, VPREB1-002, EWSR1-019, FAM134A-004, AC096579.7-001, RNU1-78P-201, SELENBP1-001, HBB-001, EBF1-001, CLC-001, RGS2-001, UCA1-001, FTH1-002, AHSP-001, SNORA22-201, TMBIM6-006, NPY-001, RGS1-001, BLOC1S1-001, VPREB3-001, and RPL14-003,
(iii) detecting and quantitating the hybridized complex to detect the RNA expression level.
12. The method of claim 11 , further comprising comparing the RNA expression level to a subject that does not have acute myeloid leukemia.
13. The method of claim 12 , wherein the acute myeloid leukemia is responsive to treatment with the compound of Formula (I) if the RNA expression level of the first set of RNA is higher than in the subject that does not have acute myeloid leukemia; or wherein the acute myeloid leukemia is responsive to treatment with the compound of Formula (I) if the RNA expression level of the second set of RNA is lower than in the subject that does not have acute myeloid leukemia.
14. The method of claim 11 , comprising detecting the expression level of 5 to 100 RNA selected from the first set or RNA and/or the second set of RNA.
15. The method of claim 14 , comprising detecting the expression level of 50 to 100 RNA selected from the first set or RNA and/or the second set of RNA.
16. A method for modulating acute myeloid leukemia stem cells, the method comprising contacting the acute myeloid leukemia stem cells with an effective amount of a splicing modulator selected from a compound of Formula (I) or a pharmaceutically acceptable salt thereof, thereby modulating the acute myeloid leukemia stem cells; wherein the compound of Formula (I) is:
wherein:
X 1 is N, O, or CH 2 ;
X 2 is O or C(R 6 )(R 7 );
R 6 and R 7 are each independently hydrogen, halogen, substituted or unsubstituted alkyl, substituted or unsubstituted aryl, —OR 12 , —OC(O)R 12 , —OC(O)OR 12 , or —OC(O)NR 13 R 14 ;
R 1 is hydrogen, —C(O)R 8 , —OC(O)R 8 , —OC(O)OR 8 , or —NHC(O)NHR 8 ;
R 2 , R 3 , R 4 , and R 5 are each independently hydrogen, substituted or unsubstituted alkyl, —OR 9 , —OC(O)R 9 , —OC(O)OR 9 , or —OC(O)NR 10 R 11 ;
R 8 , R 9 , R 10 , R 11 , R 12 , R 13 and R 14 are each independently hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; and
R 15 is hydrogen, halogen, CF 3 , CCl 3 , CBr 3 , CI 3 , or substituted or unsubstituted alkyl;
wherein:
(i) when X 2 is O, then the chiral carbon at R 2 has (R) stereochemistry, and the chiral carbon at R 4 has (S) stereochemistry; or when X 2 is O, then the chiral carbon at R 2 has (S) stereochemistry, and the chiral carbon at R 4 has (R) stereochemistry;
(ii) when R 2 is attached to a chiral carbon having (S) stereochemistry, then R 4 is attached to a chiral carbon having (S) or (R) stereochemistry; and
(iii) when X 2 is C(R 6 )(R 7 ), then the chiral carbon at R 2 has (R) stereochemistry, and the chiral carbon at R 4 has (S) stereochemistry; or when X 2 is (R 6 )(R 7 ), then the chiral carbon at R 2 has (S) stereochemistry, and the chiral carbon at R 4 has (R) stereochemistry.
17. The method of claim 15 , wherein the compound of Formula (I) is:
wherein R 1 is hydrogen or acetyl; R 6 and R 7 are each independently hydrogen, halogen, or methyl; R 9 is hydrogen or C 1 -C 4 unsubstituted alkyl; and R 15 is hydrogen or C 1 -C 4 unsubstituted alkyl.