Determination of MAPK-AP-1 pathway activity using unique combination of target genes

1. A method for correcting a calculated activity level of a MAPK-AP-1 cellular signaling pathway in a subject diagnosed with cancer, comprising:

a) calculating an activity level of an AP-1 transcription factor element in a sample isolated from the subject, wherein the activity level of the AP-1 transcription factor element in the sample is associated with MAPK-AP-1 cellular signaling, wherein the activity level of the MAPK-AP-1 cellular signaling pathway is active, and wherein the activity level of the AP-1 transcription factor element in the sample is calculated by:

i) receiving data on expression levels of at least three target genes derived from the sample, wherein the AP-1 transcription factor element controls transcription of the at least three target genes, and wherein the at least three target genes are selected from BCL2L11, CCND1, DDIT3, DNMT1, EGFR, ENPP2, EZR, FASLG, FIGF, GLRX, IL2, IVL, LOR, MMP1, MMP3, MMP9, SERPINE1, PLAU, PLAUR, PTGS2, SNCG, TIMP1, TP53, and VIM;

ii) calculating the activity level of the AP-1 transcription factor element in the sample using a calibrated pathway model, wherein the calibrated pathway model compares the expression levels of the at least three target genes in the sample with expression levels of the at least three target genes in the calibrated pathway model which define an activity level of the AP-1 transcription factor element; and,

b) calculating the activity level of the MAPK-AP-1 cellular signaling pathway in the sample based on the calculated activity level of the AP-1 transcription factor element in the sample, wherein the calculated activity level of the MAPK-AP-1 cellular signaling pathway in the sample is active;

c) selecting, based on the calculated activity level of the MAPK-AP-1 cellular signaling pathway in the sample, a specific treatment configured to correct the calculated activity level, wherein the specific treatment is a MAPK-AP-1 cellular signaling pathway inhibitor; and

d) administering, in response to the calculated activity level of the MAPK-AP-1 cellular signaling pathway in the sample and the selection of the specific treatment configured to correct the calculated activity level, the MAPK-AP-1 cellular signaling pathway inhibitor.

2. The method of claim 1 , wherein the at least three target genes are selected from CCND1, EGFR, EZR, GLRX, MMP1, MMP3, PLAU, PLAUR, SERPINE1, SNCG, and TIMP1.

3. The method of claim 1 , further comprising assigning a MAPK-AP-1 cellular signaling pathway activity status to the calculated activity level of the MAPK-AP-1 cellular signaling pathway in the sample.

4. The method of claim 3 , further comprising displaying the MAPK-AP-1 cellular signaling pathway activity status.

5. The method of claim 1 , wherein the calibrated pathway model is a probabilistic model incorporating conditional probabilistic relationships that compare the expression levels of the at least three target genes in the sample with expression levels of the at least three target genes in the calibrated pathway model which define a level of the AP-1 transcription factor element to determine the activity level of AP-1 transcription factor element in the sample.

6. The method of claim 1 , wherein the calibrated pathway model is a linear model incorporating relationships that compare the expression levels of the at least three target genes in the sample with expression levels of the at least three target genes in the calibrated pathway model which define a level of the AP-1 transcription factor element to determine the activity level of the AP-1 transcription factor element in the sample.

7. A method of treating a subject suffering from a disease associated with an activated MAPK-AP-1 cellular signaling pathway comprising:

a) receiving information regarding an activity level of a MAPK-AP-1 cellular signaling pathway derived from a sample isolated from the subject, wherein the activity level of the MAPK-AP-1 cellular signaling pathway is active, and wherein the activity level of the MAPK-AP-1 cellular signaling pathway is determined by:

i) calculating an activity level of an AP-1 transcription factor element in a sample isolated from the subject, wherein the activity level of the AP-1 transcription factor element in the sample is associated with MAPK-AP-1 cellular signaling, and wherein the activity level of the AP-1 transcription factor element in the sample is calculated by:

1) Receiving data on expression levels of at least three target genes derived from the sample, wherein the AP-1 transcription factor element controls transcription of the at least three target genes, and wherein the at least three target genes are selected from BCL2L11, CCND1, DDIT3, DNMT1, EGFR, ENPP2, EZR, FASLG, FIGF, GLRX, IL2, IVL, LOR, MMP1, MMP3, MMP9, SERPINE1, PLAU, PLAUR, PTGS2, SNCG, TIMP1, TP53, and VIM;

2) Calculating the activity level of the AP-1 transcription factor element in the sample using a calibrated pathway model, wherein the calibrated pathway model compares the expression levels of the at least three target genes in the sample with expression levels of the at least three target genes in the calibrated pathway model which define an activity level of AP-1 transcription factor element; and,

ii) calculating the activity level of the MAPK-AP-1 cellular signaling pathway in the sample based on the calculated activity level of the AP-1 transcription factor element in the sample; and,

b) administering to the subject a MAPK-AP-1 inhibitor in response to the received information regarding the activity level of the MAPK-AP-1 cellular signaling pathway.

8. The method of claim 7 , wherein the at least three target genes are selected from CCND1, EGFR, EZR, GLRX, MMP1, MMP3, PLAU, PLAUR, SERPINE1, SNCG, and TIMP1.

9. The method of claim 7 , wherein the MAPK-AP-1 inhibitor is SP600125, PD98059, PD184352, U0126, Ro092210, or LLZ16402.

10. The method of claim 7 , wherein the disease is a cancer or an immune disorder.