1. Septin 9 amplification and isoform-specific expression in peritumoral and tumor breast tissue
- Author
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Vahni Vishala Bernard, Cagdas Tazearslan, Diana Connolly, Esther Adler, Maja H. Oktay, Hien G. Hoang, Nichelle Simmons, Maria Castaldi, and Cristina Montagna
- Subjects
Adult ,Gene isoform ,Clinical Biochemistry ,Gene Dosage ,Breast Neoplasms ,Biology ,Biochemistry ,Gene dosage ,Breast cancer ,Downregulation and upregulation ,Pancreatic cancer ,Gene duplication ,medicine ,Humans ,Protein Isoforms ,Breast ,RNA, Messenger ,Molecular Biology ,Aged ,Aged, 80 and over ,Oncogene ,Gene Amplification ,Epithelial Cells ,Middle Aged ,medicine.disease ,Molecular biology ,Primary tumor ,Female ,Neoplasm Grading ,Septins - Abstract
Septins are a large family of GTP-binding proteins abnormally expressed in many solid tumors. Septin 9 (SEPT9) in particular has been found overexpressed in diverse human tumors including breast, head and neck, ovarian, endometrial, kidney, and pancreatic cancer. Although we previously reported SEPT9 amplification in breast cancer, we now show specifically that high-grade breast carcinomas, the subtype with worst clinical outcome, exhibit a significant increase in SEPT9 copy number when compared with other tumor grades. We also present, for the first time, a sensitive and quantitative measure of seven (SEPT9_v1 through SEPT9_v7) isoform variant mRNA levels in mammary epithelial cells. SEPT9_v1, SEPT9_v3, SEPT9_v6, and SEPT9_v7 isoforms were expressed at the highest levels followed by SEPT9_v2 and SEPT9_v5, whereas SEPT9_v4 was almost undetectable. Although most of the isoforms were upregulated in primary tumor tissues relative to the patient-matched peritumoral tissues, SEPT9_v4 remained the lowest expressing isoform. This comprehensive analysis of SEPT9 provides substantial evidence for increased SEPT9 expression as a consequence of genomic amplification and is the first study to profile SEPT9_v1 through SEPT9_v7 isoform-specific mRNA expression in tumor and nontumor tissues from patients with breast cancer. more...
- Published
- 2013
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