Methods and compositions for detecting and modulating an immunotherapy resistance gene signature in cancer
The subject matter disclosed herein is generally directed to detecting and modulating novel gene signatures for the treatment and prognosis of cancer. The novel gene signatures predict overall survival in cancer and can be targeted therapeutically.
1. A method of treating a cancer in a subject comprising detecting whether an immune checkpoint inhibitor resistance (ICR) gene signature is expressed in malignant cells from a solid tumor sample obtained from the subject and administering a treatment,
wherein the ICR gene signature comprises upregulation of C1QBP, CCT2, CCT6A, DCAF13, EIF4A1, ILF2, MAGEA4, NONO, PA2G4, PGAM1, PPA1, PPIA, RPL18A, RPL26, RPL31, RPS11, RPS15, RPS21, RPS5, RUVBL2, SAE1, SNRPE, UBA52, UQCRH and VDAC2; and, optionally, downregulation of AEBP1, AHNAK, APOC2, APOD, APOE, B2M, C10orf54, CD63, CTSD, EEA1, EMP1, FBXO32, FYB, GATSL3, HCP5, HLA-A, HLA-B, HLA-C, HLA-E, HLA-F, HLA-H, ITGA3, LAMP2, LYRM9, MFGE8, MIA, NPC2, NSG1, PROS1, RDH5, SERPINA1, TAPBP, TIMP2, TNFSF4 and TRIML2, as compared to a reference level,
wherein if an ICR gene signature is detected in malignant cells the treatment comprises administering an agent capable of reducing expression or activity of said signature, wherein the agent comprises a small molecule CDK4/6 inhibitor selected from the group consisting of abemaciclib, palbociclib, and ribociclib, and
wherein if an ICR gene signature is not detected the treatment comprises administering an immunotherapy.
2. The method according to claim 1 , wherein the method further comprises:
detecting whether the ICR signature is expressed in a tumor obtained from the subject after the treatment with the agent comprising a small molecule CDK4/6 inhibitor and administering an immunotherapy if said signature is reduced or below a reference level.
3. The method according to claim 1 , wherein the immunotherapy comprises a check point inhibitor or adoptive cell transfer (ACT).
4. The method according to claim 3 , wherein adoptive cell transfer comprises a CAR T cell or activated autologous T cells and wherein the checkpoint inhibitor comprises anti-CTLA4 or anti-PD1 therapy.
5. A method of treating a cancer in a subject comprising administering to the subject a therapeutically effective amount of an agent comprising a small molecule CDK4/6 inhibitor selected from the group consisting of abemaciclib, palbociclib, and ribociclib,
wherein the subject was treated with immune checkpoint inhibitors (ICI) and is resistant, and
wherein the subject has a solid tumor that expresses an ICR gene signature in malignant cells, said gene signature comprising upregulation of C1QBP, CCT2, CCT6A, DCAF13, EIF4A1, ILF2, MAGEA4, NONO, PA2G4, PGAM1, PPA1, PPIA, RPL18A, RPL26, RPL31, RPS11, RPS15, RPS21, RPS5, RUVBL2, SAE1, SNRPE, UBA52, UQCRH and VDAC2; and, optionally, downregulation of AEBP1, AHNAK, APOC2, APOD, APOE, B2M, C10orf54, CD63, CTSD, EEA1, EMP1, FBXO32, FYB, GATSL3, HCP5, HLA-A, HLA-B, HLA-C, HLA-E, HLA-F, HLA-H, ITGA3, LAMP2, LYRM9, MFGE8, MIA, NPC2, NSG1, PROS1, RDH5, SERPINA1, TAPBP, TIMP2, TNFSF4 and TRIML2, as compared to a reference level.
6. The method according to claim 5 , wherein the small molecule CDK4/6 inhibitor is abemaciclib.
7. The method according to claim 5 , wherein the method further comprises administering an immunotherapy to the subject.
8. The method of claim 7 , wherein the immunotherapy comprises a check point inhibitor.
9. The method of claim 8 , wherein the checkpoint inhibitor comprises anti-CTLA4 or anti-PD1 therapy.
10. The method according to claim 1 , wherein the small molecule CDK4/6 inhibitor is abemaciclib.