Inositol metabolism is severely impaired in follicles obtained from cystic ovaries, leading to deregulated insulin transduction and steroid synthesis. On the contrary, inositol administration to women suffering from polycystic ovary syndrome (PCOS) has been proven to efficiently counteract most of the clinical hallmarks displayed by PCOS patients, including insulin resistance, hyperandrogenism and oligo-amenorrhea. We have recently observed that myo-inositol induces significant changes in cytoske- letal architecture of breast cancer cells, by modulating different biochemical pathways, eventually mod- ulating the epithelial–mesenchymal transition. We hypothesize that inositol and its monophosphate derivatives, besides their effects on insulin transduction, may efficiently revert histological and functional features of cystic ovary by inducing cytoskeleton rearrangements. We propose an experimental model that could address not only whether inositol modulates cytoskeleton dynamics in both normal and cystic ovary cells, but also whether this effect may interfere with ovarian steroidogenesis. A more compelling understanding of the mechanisms of action of inositol (and its derivatives) would greatly improve its therapeutic utilization, by conferring to current treatments a well-grounded scientific rationale.

Does myo-inositol effect on PCOS follicles involve cytoskeleton regulation? / Bizzarri, Mariano; Cucina, Alessandra; Dinicola, Simona; Harrath, Abdel Halim; Alwasel, Saleh H.; Unfer, Vittorio; Bevilacqua, Arturo. - In: MEDICAL HYPOTHESES. - ISSN 0306-9877. - STAMPA. - 91:(2016), pp. 1-5. [10.1016/j.mehy.2016.03.014]

Does myo-inositol effect on PCOS follicles involve cytoskeleton regulation?

BIZZARRI, Mariano;CUCINA, Alessandra;DINICOLA, SIMONA;BEVILACQUA, Arturo
2016

Abstract

Inositol metabolism is severely impaired in follicles obtained from cystic ovaries, leading to deregulated insulin transduction and steroid synthesis. On the contrary, inositol administration to women suffering from polycystic ovary syndrome (PCOS) has been proven to efficiently counteract most of the clinical hallmarks displayed by PCOS patients, including insulin resistance, hyperandrogenism and oligo-amenorrhea. We have recently observed that myo-inositol induces significant changes in cytoske- letal architecture of breast cancer cells, by modulating different biochemical pathways, eventually mod- ulating the epithelial–mesenchymal transition. We hypothesize that inositol and its monophosphate derivatives, besides their effects on insulin transduction, may efficiently revert histological and functional features of cystic ovary by inducing cytoskeleton rearrangements. We propose an experimental model that could address not only whether inositol modulates cytoskeleton dynamics in both normal and cystic ovary cells, but also whether this effect may interfere with ovarian steroidogenesis. A more compelling understanding of the mechanisms of action of inositol (and its derivatives) would greatly improve its therapeutic utilization, by conferring to current treatments a well-grounded scientific rationale.
2016
Myo-inositol, PCOS, steroidogenesis, cytoskeleton
01 Pubblicazione su rivista::01a Articolo in rivista
Does myo-inositol effect on PCOS follicles involve cytoskeleton regulation? / Bizzarri, Mariano; Cucina, Alessandra; Dinicola, Simona; Harrath, Abdel Halim; Alwasel, Saleh H.; Unfer, Vittorio; Bevilacqua, Arturo. - In: MEDICAL HYPOTHESES. - ISSN 0306-9877. - STAMPA. - 91:(2016), pp. 1-5. [10.1016/j.mehy.2016.03.014]
File allegati a questo prodotto
File Dimensione Formato  
Bizzarri_Myo-inositol_2016.pdf

solo gestori archivio

Note: Articolo principale
Tipologia: Documento in Post-print (versione successiva alla peer review e accettata per la pubblicazione)
Licenza: Tutti i diritti riservati (All rights reserved)
Dimensione 284.04 kB
Formato Adobe PDF
284.04 kB Adobe PDF   Contatta l'autore

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/865984
Citazioni
  • ???jsp.display-item.citation.pmc??? 9
  • Scopus 23
  • ???jsp.display-item.citation.isi??? 20
social impact