Francesca Angileri
University of Palermo
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Featured researches published by Francesca Angileri.
Current Pharmaceutical Design | 2013
Andrea Pace; Giampaolo Barone; Antonino Lauria; Annamaria Martorana; Antonio Palumbo Piccionello; Paola Pierro; Alessio Terenzi; Anna Maria Almerico; Silvestre Buscemi; Claudia Campanella; Francesca Angileri; Francesco Carini; Giovanni Zummo; Everly Conway de Macario; Francesco Cappello; Alberto J.L. Macario
Heat shock protein 60 kDa (Hsp60) is a chaperone classically believed to be involved in assisting the correct folding of other mitochondrial proteins. Hsp60 also plays a role in cytoprotection against cell stressors, displaying for example, antiapoptotic potential. Despite the plethora of studies devoted to the mechanism of Hsp60s function, especially in prokaryotes, fundamental issues still remain unexplored, including the definition of its role in cancer. Key questions still unanswered pertain to the differences in structure-function features that might exist between the well-studied prokaryotic GroEL and the largely unexplored eukaryotic Hsp60 proteins. In this article we discuss these differences in sequence, structure, and roles of Hsp60, focusing on the human ortholog with the view of devising compounds to block its ability to favour tumor-cell growth and survival. Compounds currently known to directly or indirectly affect Hsp60 functions, such as protein folding, HIF-1α accumulation, or Hsp60-induced cell proliferation, are discussed along with strategies that might prove effective for developing Hsp60-targeting drugs for anticancer therapy.
Scientific Reports | 2015
Wonki Min; Francesca Angileri; Haibin Luo; Antonino Lauria; Maruda Shanmugasundaram; Anna Maria Almerico; Francesco Cappello; Everly Conway de Macario; Igor K. Lednev; Alberto J.L. Macario; Frank T. Robb
Chaperonins mediate protein folding in a cavity formed by multisubunit rings. The human CCT has eight non-identical subunits and the His147Arg mutation in one subunit, CCT5, causes neuropathy. Knowledge is scarce on the impact of this and other mutations upon the chaperones structure and functions. To make progress, experimental models must be developed. We used an archaeal mutant homolog and demonstrated that the His147Arg mutant has impaired oligomeric assembly, ATPase activity, and defective protein homeostasis functions. These results establish for the first time that a human chaperonin gene defect can be reproduced and studied at the molecular level with an archaeal homolog. The major advantage of the system, consisting of rings with eight identical subunits, is that it amplifies the effects of a mutation as compared with the human counterpart, in which just one subunit per ring is defective. Therefore, the slight deficit of a non-lethal mutation can be detected and characterized.
Journal of Medicinal Chemistry | 2013
Antonino Lauria; Ilenia Abbate; Carla Gentile; Francesca Angileri; Annamaria Martorana; Anna Maria Almerico
The design through energy-based pharmacophore virtual screening has led to aminocyanopyridine derivatives as efficacious new inhibitors of Hsp90. The synthesized compounds showed a good affinity for the Hsp90 ATP binding site in the competitive binding assay. Moreover, they showed an excellent antiproliferative activity against a large number of human tumor cell lines. Further biological studies on the derivative with the higher EC50 confirmed its specific influence on the cellular pathways involving Hsp90.
Scientific Reports | 2016
Chong Tian; Qiao Huang; Liangle Yang; Sébastien Légaré; Francesca Angileri; Handong Yang; Xiulou Li; Xinwen Min; Ce Zhang; Chengwei Xu; Jing Yuan; Xiaoping Miao; Meian He; Tangchun Wu; Xiaomin Zhang
Prospective studies on the association of green tea with risk of coronary heart disease (CHD) incidence were scarce. This study examined whether green tea can reduce CHD incidence and have a beneficial effect on CHD-related risk markers in middle-aged and older Chinese population. We included 19 471 participants who were free of CHD, stroke or cancer at baseline from September 2008 to June 2010, and were followed until October 2013. Cox proportional hazard models were used to examine the hazard ratios (HR) of CHD incidence in relation to green tea consumption. Linear regression models were used to evaluate the effect of green tea on 5-year changes of CHD-related biomarkers. Compared with non-green tea consumers, the multivariable-adjusted HR for CHD was 0.89 (95% CI, 0.81-0.98) in green tea consumers. Particularly, the reduced risk of CHD incidence with green tea consumption was more evident among participants who were male, more than 60 years old, overweight, or with diabetes mellitus. In addition, green tea consumption improved multiple CHD-related risk markers including total cholesterol, HDL-cholesterol, triglycerides, mean platelet volume, and uric acid. In conclusion, green tea consumption was associated with a reduced risk of CHD incidence in the middle-aged and older Chinese populations, and the association might be partly due to altered CHD-related biomarkers.
Current Pharmaceutical Design | 2012
Francesco Cappello; Francesca Angileri; Everly Conway de Macario; Alberto J.L. Macario
In this minireview we focus on Hsp60 as a target for anticancer therapy. We discuss the new concepts of chaperonopathies and chaperonotherapy and present information on Hsp60 localization in the cell membrane of human tumor cells. We describe novel mechanisms for Hsp60 reaching the extracellular environment that involve membrane-associated stages, as well as data on anti-Hsp60 antibodies found in human sera, both in normal subjects and patients affected by autoimmune diseases. Finally, we discuss possible therapeutic applications of anti-Hsp60 antibodies in cancer treatment, evaluating also side effects on non-tumor cells. In conclusion, the way for investigating Hsp60-targeted anti-tumor therapy is open, at least for those tumors that express Hsp60 on its surface and/or secrete it outside the cell, as is the search for the molecular mechanisms involved in Hsp60 translocation from cytosol to cell membrane: elucidation of this mechanism will greatly facilitate the optimization of chaperonotherapy centered on Hsp60 with anti-tumor efficacy and minimal side effects.
Journal of Neurosurgical Sciences | 2015
Giovanni Raffa; La Torre D; Alfredo Conti; Salvatore Cardali; Francesca Angileri; Antonino Germanò
BACKGROUND Ventriculoperitoneal (VP) shunt is one of the options for the treatment of hydrocephalus. The aim of this study is to describe the efficacy and safety of a 90cm-long peritoneal catheter in newborns and infants treated for hydrocephalus. We analyzed the incidence of distal-related complications and the need of successive surgeries for malfunction or for lengthening of the peritoneal catheter. METHODS We reviewed medical records of neonates and infants treated with a VP shunt using a 90cm-long peritoneal catheter. Function and integrity of shunts were assessed through abdominal echographic studies, skull, neck, chest and abdomen X-rays. We compared shunt revision rates due to distal complications and insufficient length of the peritoneal catheter in the study group with an historical control group composed by newborns and infants treated with a standard VP shunt at our Institution during the last twenty years. RESULTS Three neonates and 3 infants were treated with the insertion of the 90cm-long distal catheter into the peritoneal cavity for its total length. The mean follow-up was 7.6 years. As compared to controls, in the study group the revision rate for distal complications was not significantly increased (P=0.33), whereas revision surgeries due to insufficient peritoneal catheter length were significantly reduced (P=0.04). CONCLUSIONS This study demonstrates for the first time that the use of 90cm-long peritoneal catheters in neonates and infants is a safe and effective procedure. It does not increase the incidence of abdominal complications, avoiding the need of revision for insufficient length of the peritoneal catheter.
European Journal of Nutrition | 2013
Luisa Tesoriere; Carla Gentile; Francesca Angileri; Alessandro Attanzio; Marco Tutone; Mario Allegra; M. A. Livrea
European Journal of Nutrition | 2012
Carla Gentile; Mario Allegra; Francesca Angileri; Anna Maria Pintaudi; M. A. Livrea; Luisa Tesoriere
Sleep | 2016
Liangle Yang; Zengguang Xu; Meian He; Handong Yang; Xiulou Li; Xinwen Min; Ce Zhang; Chengwei Xu; Francesca Angileri; Sébastien Légaré; Jing Yuan; Xiaoping Miao; Huan Guo; Ping Yao; Tangchun Wu; Xiaomin Zhang
Archive | 2011
Maria A. Livrea; Luisa Tesoriere; Anna Maria Pintaudi; Mario Allegra; Carla Gentile; Francesca Angileri; Pintaudi. A M; Alessandro Attanzio; M. A. Livrea