BIOMARKERS FOR BREAST CANCER
Methods and compositions are provided for the detection of breast cancer based upon the identification of three biomarkers for non-normal breast cells. The biomarkers were identified based upon multiple sampling of reference breast tissue samples from independent cases of breast cancer. Two biomarkers display increased expression in non-normal cells while the third biomarker displays decreased expression in non-normal cells.
1 . A method to determine the presence of pre-malignant cells in a sample from a human subject comprising assaying a sample suspected of containing pre-malignant cells for decreased expression of human ESE-2/ELF5 sequences.
2 . The method of claim 1 wherein said sample is from a subject afflicted with, or suspected of having, atypical ductal hyperplasia (ADH) or breast cancer.
3 . The method of claim 1 wherein said sample is obtained by solid tissue biopsy or a non-invasive procedure.
4 . The method of claim 3 wherein said non-invasive procedure is selected from ductal lavage, fine needle aspiration, or a needle biopsy.
5 . The method of claim 4 wherein microdissection is used to isolate breast cells from said sample before assaying for nucleic acid expression.
6 . The method of claim 5 wherein said assaying is by hybridization to a polynucleotide comprising sequences of at least 24 nucleotides from the 3′ untranslated region, the coding region, or the 5′ untranslated region, of human ESE-2/ELF5.
7 . The method of claim 1 wherein said assaying is by PCR amplification of said ESE-2/ELF5 sequence.
8 . The method of claim 7 wherein said assaying is by quantitative PCR.
9 . The method of claim 1 wherein said assaying is for inactivation or methylation of ESE-2/ELF5 sequences.
10 . The method of claim 1 wherein said assaying comprises detection of increased mRNA degradation.
11 . A method to determine the presence of non-normal or abnormal breast cells in a sample from a human subject comprising assaying said sample for increased expression of one or more human CRIP1 or HN1 sequences.