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Buchner, Johannes

Biological Chemistry

Editor-in-Chief: Brüne, Bernhard

Editorial Board Member: Buchner, Johannes / Lei, Ming / Ludwig, Stephan / Sies, Helmut / Turk, Boris / Wittinghofer, Alfred


SCImago Journal Rank (SJR) 2015: 1.607
Source Normalized Impact per Paper (SNIP) 2015: 0.751
Impact per Publication (IPP) 2015: 2.609

Online
ISSN
1437-4315
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Mid-region parathyroid hormone-related protein (PTHrP) and gene expression of MDA-MB231 breast cancer cells

Rosalia Sirchia1 / Claudio Luparello2

1Dipartimento di Biologia Cellulare e dello Sviluppo, Università di Palermo, I-90128 Palermo, Italy

2Dipartimento di Biologia Cellulare e dello Sviluppo, Università di Palermo, I-90128 Palermo, Italy

Corresponding author

Citation Information: Biological Chemistry. Volume 388, Issue 5, Pages 457–465, ISSN (Online) 14316730, ISSN (Print) 14374315, DOI: https://doi.org/10.1515/BC.2007.059, May 2007

Publication History

Received:
2006-11-30
Accepted:
2007-02-14
Published Online:
2007-05-01

Abstract

We have previously shown that PTHrP(38–94) amide restrains growth and invasion in vitro, causes striking toxicity and accelerates death of some breast cancer cell lines, the most responsive being MDA-MB231, for which tumorigenesis was also attenuated in vivo. We have also demonstrated that mid-region PTHrP gains access to the nuclear compartment of these cells and displays DNA-binding properties in vitro by recognizing targets in both cellular chromatin and isolated oligonucleotides. Here, we examined whether PTHrP(38–94) amide was able to modulate gene expression of MDA-MB231 cells, employing a combination of conventional, differential display and semi-quantitative multiplex PCR techniques. The results obtained provide first evidence that PTHrP(38–94) amide can affect gene expression in tumor cells, identifying A4-differentiation protein/PLP2 as up-regulated, and HOX7/MSX1, COX6C, FZD6, OXR1 and TMCO4 as down-regulated genes in treated cells, and suggest that the cytotoxic activity of the peptide can be ascribed, at least in part, to such transcriptional reprogramming.

Keywords: breast cancer; differential display; gene expression; PCR; PTHrP

Citing Articles

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[2]
Claudio Luparello, Rosalia Sirchia, and Alessandra Longo
Molecular Carcinogenesis, 2013, Volume 52, Number 5, Page 348
[3]
Claudio Luparello, Alessandra Longo, and Marco Vetrano
Biochimie, 2012, Volume 94, Number 1, Page 207
[4]
Richard N. Re and Julia L. Cook
Journal of the American Society of Hypertension, 2011, Volume 5, Number 6, Page 435
[6]
Claudio Luparello, Rosalia Sirchia, and Bruna Lo Sasso
Breast Cancer Research and Treatment, 2008, Volume 111, Number 3, Page 461

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