http://www.cnr.it/ontology/cnr/individuo/prodotto/ID215486
Regulation of the expression of CLU isoforms in endometrial proliferative diseases (Articolo in rivista)
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- Regulation of the expression of CLU isoforms in endometrial proliferative diseases (Articolo in rivista) (literal)
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- 2013-01-01T00:00:00+01:00 (literal)
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- Alternative label
Fuzio P, Valletti A, Napoli A, Napoli G, Cormio G, Selvaggi L, Liuni S, Pesole
G, Maiorano E, Perlino E. (2013)
Regulation of the expression of CLU isoforms in endometrial proliferative diseases
in International Journal of Oncology (Athens); D.A. Spandidos, Athens (Grecia)
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- Fuzio P, Valletti A, Napoli A, Napoli G, Cormio G, Selvaggi L, Liuni S, Pesole
G, Maiorano E, Perlino E. (literal)
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- 1Institute of Biomedical Technologies, ITB-CNR, I-70126 Bari; 2Institute of Biomembranes and Bioenergetics,
IBBE-CNR, I-70126 Bari; 3Department of Biosciences, Biotechnology and Biopharmaceutics, I-70126 Bari;
4Interdisciplinary Department of Medicine, University of Bari 'Aldo Moro', I-70124 Bari; 5Department of
Pathological Anatomy and Genetics, Hospital of SS. Annunziata, I-74100 Taranto; 6Department of Biomedical Sciences and Human Oncology, DIMO, University of Bari 'Aldo Moro', I-70124 Bari, Italy (literal)
- Titolo
- Regulation of the expression of CLU isoforms in endometrial proliferative diseases (literal)
- Abstract
- Clusterin (CLU) is a nearly ubiquitous multifunctional protein synthesized in different functionally divergent isoforms, sCLU and nCLU, playing a crucial role by keeping a balance between cell proliferation and death. Studying in vivo CLU expression we found a higher mRNA expression both in neoplastic and hyperplastic tissues in comparison to normal endometria; in particular, by RT-qPCR we demonstrated an increase of the specific sCLU isoform in the neoplastic and hyperplastic endometrial diseases. On the contrary, no CLU increase was detected at the protein level. The CLU gene transcriptional activity was upregulated in the hyperplastic and neoplastic tissues, indicating the existence of a fine post-trans-criptional regulation of CLU expression possibly responsible for the protein decrease in the malignant disease. A specific CLU immunoreactivity was present in all the endometrial glandular cells in comparison to the other cellular compartments where CLU immunoreactivity was lower or absent. In conclusion, our results suggest the existence of a complex regulatory mechanism of CLU gene expression during the progression from normal to malignant cells, possibly contributing to endometrial carcinogenesis. Moreover, the specific alteration of the sCLU:nCLU ratio associated with the pathological stage, suggests a possible usage of CLU as molecular biomarker for the diagnosis/prognosis of endometrial proliferative diseases. (literal)
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