Biomarkers of response to proteasome inhibitors
View Patent ↗Disclosed are markers associated with sensitivity to treatment with proteasome inhibitors. Sensitivity is observed when RAS gene is wild type in tumor cells. Compositions and methods are further provided to assess markers of marker genes to predict outcome of treatment using proteasome inhibitors to patients having a solid tumor, such as a lung tumor or a colon tumor.
1. A method for treating a patient having a solid tumor comprising wild type KRAS status, comprising the step of administering to the patient a therapeutically effective amount of Ixazomib citrate, MLN2238 or a boronate ester thereof, wherein the solid tumor comprising wild type KRAS status is selected from the group consisting of a lung tumor and a colon tumor.
2. The method of claim 1 , further comprising the steps of:
a) measuring at least one characteristic of at least one marker associated with at least one marker gene in a patient sample comprising tumor cells, wherein the at least one characteristic is selected from the group consisting of size, sequence, composition, activity and amount, and wherein at least one marker gene is v-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog (KRAS);
b) identifying whether the at least one characteristic measured in step a) is informative for outcome of treatment with the compound; and
c) administering the Ixazomib citrate, MLN2238 or a boronate ester thereof to the patient with tumor cells that comprise wild type KRAS.
3. The method of claim 2 , wherein the at least one marker is selected from the group consisting of nucleic acid and protein corresponding to the at least one marker gene.
4. The method of claim 3 , wherein the at least one marker is sequence.
5. The method of claim 3 , wherein the at least one marker is nucleic acid.
6. The method of claim 5 , wherein the nucleic acid is selected from the group consisting of DNA, mRNA and cDNA or a portion of any of the foregoing, wherein the portion comprises at least one mutation site of the at least one marker gene.
7. The method of claim 6 , wherein the nucleic acid comprises a codon of SEQ ID NO:2 selected from the group consisting of codon 12, codon 13 and codon 61, or a variant thereof, or a complement thereof.
8. The method of claim 2 , wherein the at least one marker gene is at least two marker genes.
9. The method of claim 1 , wherein the amount of GLUT4 in the patient sample is measured.
10. The method of claim 8 , wherein the amount of GLUT4 in the patient sample is measured.
11. The method of claim 10 , wherein the amount of GLUT4 is normal or low.
12. The method of claim 2 , wherein the sample comprises tumor exudate.
13. The method of claim 12 , further comprising enriching the sample for tumor cells.
14. The method of claim 9 , wherein the amount of GLUT4 is normal or low.
15. The method of claim 1 , wherein the wild type KRAS status is identified from a sample that comprises tumor exudate.
16. The method of claim 15 , further comprising enriching the sample for tumor cells.
17. The method of claim 1 , wherein the Ixazomib citrate, MLN2238 or a boronate ester thereof is the compound of formula (III-A):
or a pharmaceutically acceptable salt or a pharmaceutical composition thereof.
18. The method of claim 2 , wherein the Ixazomib citrate, MLN2238 or a boronate ester thereof is the compound of formula (III-A):
or a pharmaceutically acceptable salt or a pharmaceutical composition thereof.