Method of predicting and reducing risk of metastasis of breast cancer to lung

摘要

A signature for breast cancer tissue derived from a patient is established that is indicative of the virulence and risk of lung metastasis by determining the expression levels to define a sample signature, and comparing this sample signature to a reference signature. This determination is used to define appropriate treatment and monitoring options for the patient. Risk of metastasis to the lung can be reduced by treatment with a therapeutic combination that either (1) contains a first agent effective to inhibit epiregulin activity and a second agent effective to inhibit activity of a protein selected from the group consisting of MMP1, MMP2 and PTGS2, or (2) contains a therapeutic agent or combination of agents effective to inhibit activity MMP1, MMP2 and PTGS2. Agents that inhibit the CXCL1 pathway also can be used individually or in combination with these combinations.

主权项

1. A method for evaluating breast cancer tissue derived from a patient, comprising the steps of:
(a) obtaining a sample of breast cancer tissue from the patient, (b) evaluating the sample of breast cancer tissues to determine expression levels of plurality of genes selected from the group consisting of SPARC, IL13RA2, KLRC1 and KLRC2, MMP1, KYNU, EREG, TNC, ISG20, ALDH3A1, KRTHB1, PTGS2, LAPTM5, C10orf116, ROBO1, SPANXC, ANGPTL4, FSCN1, SOX4, SPANXB1 and SPANXC, COL6A1, CXCL1, MMP2, STOM, GPR153, MAN1A1, C14orf139, CASP1, IGSF4, LTBP1, NR2F1, EMP1, ID1, CNOT2, VCAM1, OLFML2A, NEDD9, CSF2RA, MOCOS, EPHX1, MBNL2, LOC388483, GSN, MYH10, ARNT2, RARRES3, EFEMP1, MATN2, LY6E, HLA-DPA1, ASMTL, ABCC3, KIAA1199, CXCR4, and PARD6B to obtain a sample signature for the cancer tissue sample, wherein the evaluation is performed by a method selected from the group consisting of binding of complementary oligonucleotide probes, RT-PCR, nucleic acid microarray analysis, binding of RNA specific antibodies, protein-ligand binding assays, protein immunoassays and protein microarray assays, and (c) comparing the sample signature to a reference signature, wherein the reference signature defines a standard expression level for each gene and a significant change direction for each gene, wherein the significant change direction is upregulation if the gene is SPARC, IL13RA2, KLRC1 and KLRC2, MMP1, KYNU, EREG, TNC, ISG20, ALDH3A1, KRTHB1, PTGS2, LAPTM5, C10orf116, ROBO1, SPANXC, ANGPTL4, FSCN1, SOX4, SPANXB1 and SPANXC, COL6A1, CXCL1, MMP2, STOM, GPR153, MAN1A1, C14orf139, CASP1, IGSF4, LTBP1, NR2F1, EMP1, ID1, CNOT2, or VCAM1 and downregulation if the gene is OLFML2A, NEDD9, CSF2RA, MOCOS, EPHX1, MBNL2, LOC388483, GSN, MYH10, ARNT2, RARRES3, EFEMP1, MATN2, LY6E, HLA-DPA1, ASMTL, ABCC3, KIAA1199, CXCR4, or PARD6B, and wherein a difference in the expression level in the sample signature that differs from the reference signature level for the gene in the significant change direction for the gene for at least a predetermined number of the genes tested is indicative that the patient has an increased risk of lung metastasis of the breast cancer.