Overexpression of lipid metabolism genes and PBX1 in the contralateral breasts of women with estrogen receptor‐negative breast cancer. Issue 11 (21st March 2017)

• Record Type: Journal Article
• Authors: Wang, Jun; Shidfar, Ali; Ivancic, David; Ranjan, Manish; Liu, Liannian; Choi, Mi‐Ran; Parimi, Vamsi; Gursel, Demirkan B.; Sullivan, Megan E.; Najor, Matthew S.; Abukhdeir, Abde M.; Scholtens, Denise; Khan, Seema A.
• Is Part Of: International journal of cancer. Volume 140:Issue 11(2017:Jun. 01)
• Page Start: 2484
• Page End: 2497
• Publication Date: 2017-03-21
• Subjects: lipid metabolism -- estrogen receptor -- PBX1 -- contralateral breast; Cancer -- Periodicals; Cancer -- Prevention -- Periodicals; 616.994
• DOI: 10.1002/ijc.30680
• Languages: English
• ISSNs: 0020-7136

Abstract

Abstract : Risk biomarkers for estrogen receptor (ER)‐negative breast cancer have clear value for breast cancer prevention. We previously reported a set of lipid metabolism (LiMe) genes with high expression in the contralateral unaffected breasts (CUBs) of ER‐negative cancer cases. We now further examine LiMe gene expression in both tumor and CUB, and investigate the role of Pre‐B‐cell leukemia homeobox‐1 (PBX1) as a candidate common transcription factor for LiMe gene expression. mRNA was extracted from laser‐capture microdissected epithelium from tumor and CUB of 84 subjects (28 ER‐positive cases, 28 ER‐negative cases, 28 healthy controls). Gene expression was quantitated by qRT‐PCR. Logistic regression models were generated to predict ER status of the contralateral cancer. Protein expression of HMGCS2 and PBX1 was measured using immunohistochemistry. The effect of PBX1 on LiMe gene expression was examined by overexpressing PBX1 in MCF10A cells with or without ER, and by suppressing PBX1 in MDA‐MB‐453 cells. The expression of DHRS2, HMGCS2, UGT2B7, UGT2B11, ALOX15B, HPGD, UGT2B28 and GLYATL1 was significantly higher in ER‐negative versus ER‐positive CUBs, and predicted ER status of the tumor in test and validation sets. In contrast, LiMe gene expression was significantly lower in ER‐negative than ER‐positive tumors. PBX1 overexpression in MCF10A cells up‐regulated most LiMe genes, but not in MCF10A cells overexpressing ER. Suppressing PBX1 in MDA‐MB‐453 cells resulted in decrease of LiMe gene expression. Four binding sites of PBX1 and cofactor were identified in three lipid metabolism genes using ChIP‐qPCR. These data suggest a novel role for PBX1 in the regulation of lipid metabolism genes in benign breast, which may contribute to ER‐negative tumorigenesis. Abstract : What's new? The contralateral breast is the focus of intense interest in breast cancer research. Here the authors find a set of lipid metabolism genes highly expressed in the unaffected breast of women with estrogen (ER)‐negative breast cancer. They identify the transcription factor PBX1 as a master regulator controlling expression of these genes in cell line models. Importantly, expression of the lipid metabolism genes predicted ER status of the tumor in the affected breast, implicating metabolic pathways in the genesis of ER‐negative breast cancer.