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The clinicopathological significance of lamin A/C, lamin B1 and lamin B receptor mRNA expression in human breast cancer.
- Source :
-
Cellular & molecular biology letters [Cell Mol Biol Lett] 2013 Dec; Vol. 18 (4), pp. 595-611. Date of Electronic Publication: 2013 Nov 30. - Publication Year :
- 2013
-
Abstract
- Lamin A/C (LMNA), lamin B1 (LMNB1) and lamin B receptor (LBR) have key roles in nuclear structural integrity and chromosomal stability. In this study, we have studied the relationships between the mRNA expressions of A-type lamins, LMNB1 and LBR and the clinicopathological parameters in human breast cancer. Samples of breast cancer tissues (n = 115) and associated non-cancerous tissue (ANCT; n = 30) were assessed using reverse transcription and quantitative PCR. Transcript levels were correlated with clinicopathological data. Higher levels of A-type lamins and LMNB1 mRNA expression were seen in ANCT. Higher lamin A/C expression was associated with the early clinical stage (TNM1 vs. TNM3 - 13 vs. 0.21; p = 0.0515), with better clinical outcomes (disease-free survival vs. mortality - 11 vs. 1; p = 0.0326), and with better overall (p = 0.004) and disease-free survival (p = 0.062). The expression of LMNB1 declined with worsening clinical outcome (disease-free vs. mortalities - 0.0011 vs. 0.000; p = 0.0177). LBR mRNA expression was directly associated with tumor grade (grade 1 vs. grade 3 - 0.00 vs. 0.00; p = 0.0479) and Nottingham Prognostic Index (NPI1 vs. NPI3 - 0.00 vs. 0.00; p = 0.0551). To the best of our knowledge, this is the first study to suggest such a role for A-type lamins, lamin B1 and LBR in human breast cancer, identifying an important area for further research.
- Subjects :
- Breast metabolism
Cell Cycle
Chromosomal Instability
Female
Gene Expression Regulation, Neoplastic
Humans
RNA, Messenger genetics
Lamin B Receptor
Breast pathology
Breast Neoplasms genetics
Breast Neoplasms pathology
Lamin Type A genetics
Lamin Type B genetics
Receptors, Cytoplasmic and Nuclear genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1689-1392
- Volume :
- 18
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Cellular & molecular biology letters
- Publication Type :
- Academic Journal
- Accession number :
- 24293108
- Full Text :
- https://doi.org/10.2478/s11658-013-0109-9