Santina Di Bella

Dr. Santina Di Bella

orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2012 in Cell Biology International
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AGAnnalisa Guercio
Annalisa Guercio
PMPatrizia Di Marco
Patrizia Di Marco
SCStefania Casella
Stefania Casella
VCVincenza Cannella
Vincenza Cannella
LRLaura Russotto
Laura Russotto
GPGiuseppe Piccione
Giuseppe Piccione

30 October 2019 in BioMed Research International
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VCVincenza Cannella
Vincenza Cannella
RARoberta Altomare
Roberta Altomare
GCGabriele Chiaramonte
Gabriele Chiaramonte
SBSantina Di Bella
Santina Di Bella
FMFrancesco Mira
Francesco Mira
AGAnnalisa Guercio
Annalisa Guercio
Objective. The aim of this study was to evaluate the cytotoxic potential of a type of endodontic pin on L929 cell line according to the UNI EN ISO 10993/2009 rule. Methods. L929 cells were used for the assays; extracts were prepared from three different-diameter endodontic pins, made of epoxy resin and fiberglass matrix and from Reference Materials (ZDEC, ZDBC, and HDP films). MTS assay was performed after 24 h, 48 h, and 72 h of exposure of L929 cells to pin and Reference Material extracts, 5% phenol solution, and control reagent. Cells cultured with different media containing extracts were monitored for up to 72 h and stained with haematoxylin/eosin. Results. Pins of different diameters had no cytotoxic effects on L929 cells at 24 h, 48 h, and 72 h (all values >70%). Cells cultured in medium containing pin extracts grew without any differences compared to the control cells. Conclusion. The endodontic pins tested showed no cytotoxic effects and did not induce changes in morphology for up to 72 h.

31 October 2013 in Cell Death & Disease
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Antonella D'AnneoAntonella D'Anneo
Antonella D'Anneo
DCDaniela Carlisi
Daniela Carlisi
MLM Lauricella
M Lauricella
RPRoberto Puleio
Roberto Puleio
RMR Martinez
R Martinez
GTG Tesoriere
G Tesoriere
Triple-negative breast cancers (TNBCs) are clinically aggressive forms associated with a poor prognosis. We evaluated the cytotoxic effect exerted on triple-negative MDA-MB231 breast cancer cells both by parthenolide and its soluble analogue dimethylamino parthenolide (DMAPT) and explored the underlying molecular mechanism. The drugs induced a dose- and time-dependent decrement in cell viability, which was not prevented by the caspase inhibitor z-VAD-fmk. In particular in the first hours of treatment (1–3 h), parthenolide and DMAPT strongly stimulated reactive oxygen species (ROS) generation. The drugs induced production of superoxide anion by activating NADPH oxidase. ROS generation caused depletion of thiol groups and glutathione, activation of c-Jun N-terminal kinase (JNK) and downregulation of nuclear factor kB (NF-kB). During this first phase, parthenolide and DMAPT also stimulated autophagic process, as suggested by the enhanced expression of beclin-1, the conversion of microtubule-associated protein light chain 3-I (LC3-I) to LC3-II and the increase in the number of cells positive to monodansylcadaverine. Finally, the drugs increased RIP-1 expression. This effect was accompanied by a decrement of pro-caspase 8, while its cleaved form was not detected and the expression of c-FLIPS markedly increased. Prolonging the treatment (5–20 h) ROS generation favoured dissipation of mitochondrial membrane potential and the appearance of necrotic events, as suggested by the increased number of cells positive to propidium iodide staining. The administration of DMAPT in nude mice bearing xenografts of MDA-MB231 cells resulted in a significant inhibition of tumour growth, an increment of animal survival and a marked reduction of the lung area invaded by metastasis. Immunohistochemistry data revealed that treatment with DMAPT reduced the levels of NF-kB, metalloproteinase-2 and -9 and vascular endothelial growth factor, while induced upregulation of phosphorylated JNK. Taken together, our data suggest a possible use of parthenolide for the treatment of TNBCs.

1 March 2019 in International Journal of Infectious Diseases
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Journal Article
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GPGiuseppa Purpari
Giuseppa Purpari
GMGIUSI MACALUSO
GIUSI MACALUSO
SBSantina Di Bella
Santina Di Bella
FGFrancesca Gucciardi
Francesca Gucciardi
FMFrancesco Mira
Francesco Mira
AGAnnalisa Guercio
Annalisa Guercio
Enteric viruses are responsible for foodborne and waterborne infections affecting a large number of people. Data on food and water viral contamination in the south of Italy (Sicily) are scarce and fragmentary. The aim of this study was to evaluate the presence of viral contamination in food, water samples, and surface swabs collected in Sicily METHODS: The survey was conducted on 108 shellfish, 23 water samples (seawater, pipe water, and torrent water), 52 vegetables, one peach and 17 berries, 11 gastronomic preparations containing fish products and/or raw vegetables, and 28 surface swabs. Hepatitis A virus (HAV), genogroup GI, GII, and GIV norovirus (NoV), enterovirus (EV), rotavirus (RoV), hepatitis E virus (HEV), adenovirus (AdV), and bocavirus (BoV) were detected by nested (RT) PCR, real-time PCR, and sequence analysis. The most frequently detected viruses in shellfish were HAV (13%), NoV (18.5%), and EV (7.4%). Bocavirus was found in 3.7%, HEV in 0.9%, and AdV in 1.9% of the molluscs. Of the 23 water samples, 21.7% were positive for GII NoV and 4.3% for RoV and HEV genotype 3. Of the 70 vegetable samples, 2.9% were positive for NoV GI (GI.5 and GI.6), 2.9% for EV, and 1.4% for HEV. In the gastronomic preparations, only one EV (9%) was detected. No enteric viruses were detected in the berries, fruit, or swabs analyzed. Molecular surveillance of water and food samples clearly demonstrated that human pathogenic viruses are widely found in aquatic environments and on vegetables, and confirmed the role of vegetables and bivalve molluscs as the main reservoirs.

13 November 2017 in Transboundary and Emerging Diseases
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FMFrancesco Mira
Francesco Mira
GPG. Purpari
G. Purpari
ELE. Lorusso
E. Lorusso
SBSantina Di Bella
Santina Di Bella
FGFrancesca Gucciardi
Francesca Gucciardi
AGA. Guercio
A. Guercio

15 March 2013 in Cell Biology International
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AGAnnalisa Guercio
Annalisa Guercio
SBSantina Di Bella
Santina Di Bella
SCStefania Casella
Stefania Casella
PMPatrizia Di Marco
Patrizia Di Marco
CRCarmelo Russo
Carmelo Russo
GPGiuseppe Piccione
Giuseppe Piccione