Mirella Falconi

Mirella Falconi


Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

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

Representative Publications

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24 December 2016 in Oncotarget
Verified
Journal Article
Open access
PDF file
VSViviana Salvatore
Viviana Salvatore
GTGabriella Teti
Gabriella Teti
SFStefano Focaroli
Stefano Focaroli
MMMaria Carla Mazzotti
Maria Carla Mazzotti
Antonio MazzottiAntonio Mazzotti
Antonio Mazzotti
MFMirella Falconi
Mirella Falconi
The tumor microenvironment promotes cancer progression and cell migration

1 September 2014 in Carbohydrate Polymers
Verified
Journal Article
Closed access
MMMonica Mattioli-Belmonte
Monica Mattioli-Belmonte
SCStefania Cometa
Stefania Cometa
CFConcetta Ferretti
Concetta Ferretti
RIRoberta Iatta
Roberta Iatta
ATAdriana Trapani
Adriana Trapani
Elvira De GiglioElvira De Giglio
Elvira De Giglio

13 March 2018 in Stem Cells International
Verified
Journal Article
Open access
PDF file
GTGabriella Teti
Gabriella Teti
SFStefano Focaroli
Stefano Focaroli
VSViviana Salvatore
Viviana Salvatore
EMEleonora Mazzotti
Eleonora Mazzotti
LILaura Ingra’
Laura Ingra’
MFMirella Falconi
Mirella Falconi
Adult stem cells are a promising cell source for cartilage regeneration. They resided in a special microenvironment known as the stem-cell niche, characterized by the presence of low oxygen concentration. Cobalt chloride (CoCl2) imitates hypoxia in vitro by stabilizing hypoxia-inducible factor-alpha (HIF-1α), which is the master regulator in the cellular adaptive response to hypoxia. In this study, the influence of CoCl2 on the chondrogenic potential of human MSCs, isolated from dental pulp, umbilical cord, and adipose tissue, was investigated. Cells were treated with concentrations of CoCl2 ranging from 50 to 400 μM. Cell viability, HIF-1α protein synthesis, and the expression of the chondrogenic markers were analyzed. The results showed that the CoCl2 supplementation had no effect on cell viability, while the upregulation of chondrogenic markers such as SOX9, COL2A1, VCAN, and ACAN was dependent on the cellular source. This study shows that hypoxia, induced by CoCl2 treatment, can differently influence the behavior of MSCs, isolated from different sources, in their chondrogenic potential. These findings should be taken into consideration in the treatment of cartilage repair and regeneration based on stem cell therapies.

Verified
Journal Article
Open access
PDF file
Manuela DicarloManuela Dicarlo
Manuela Dicarlo
GTGabriella Teti
Gabriella Teti
Giulio VernaGiulio Verna
Giulio Verna
MLMarina Liso
Marina Liso
ECElisabetta Cavalcanti
Elisabetta Cavalcanti
Marcello ChieppaMarcello Chieppa
Marcello Chieppa
Inflammatory bowel diseases (IBDs) are chronic and relapsing immune disorders that result, or possibly originate, from epithelial barrier defects. Intestinal organoids are a new reliable tool to investigate epithelial response in models of chronic inflammation. We produced organoids from the ulcerative colitis murine model Winnie to explore if the chronic inflammatory features observed in the parental intestine were preserved by the organoids. Furthermore, we investigated if quercetin administration to in vitro cultured organoids could suppress LPS-induced inflammation in wild-type organoids (WT-organoids) and spontaneous inflammation in ulcerative colitis organoids (UC-organoids). Our data demonstrate that small intestinal organoids obtained from Winnie mice retain the chronic intestinal inflammatory features characteristic of the parental tissue. Quercetin administration was able to suppress inflammation both in UC-organoids and in LPS-treated WT-organoids. Altogether, our data demonstrate that UC-organoids are a reliable experimental system for investigating chronic intestinal inflammation and pharmacological responses.

4 May 2007 in Cell Biology and Toxicology
Verified
Journal Article
Closed access
PDF file
MFMirella Falconi
Mirella Falconi
GTGabriella Teti
Gabriella Teti
MZM. Zago
M. Zago
SPS. Pelotti
S. Pelotti
Lorenzo BreschiLorenzo Breschi
Lorenzo Breschi
GMG. Mazzotti
G. Mazzotti

ABAnna Bartoletti-Stella
Anna Bartoletti-Stella
VGValentina Gatta
Valentina Gatta
GMGiulia Adalgisa Mariani
Giulia Adalgisa Mariani
Pietro GobbiPietro Gobbi
Pietro Gobbi
MFMirella Falconi
Mirella Falconi
Sara SalucciSara Salucci
Sara Salucci
Most medical and health science schools adopt innovative tools to implement the teaching of anatomy to their undergraduate students. The increase in technological resources for educational purposes allows the use of virtual systems in the field of medicine, which can be considered decisive for improving anatomical knowledge, a requisite for safe and competent medical practice. Among these virtual tools, the Anatomage Table 7.0 represents, to date, a pivotal anatomical device for student education and training medical professionals. This review focuses attention on the potential of the Anatomage Table in the anatomical learning process and clinical practice by discussing these topics based on recent publication findings and describing their trends during the COVID-19 pandemic period. The reports documented a great interest in and a positive impact of the use of this technological table by medical students for teaching gross anatomy. Anatomage allows to describe, with accuracy and at high resolution, organ structure, vascularization, and innervation, as well as enables to familiarize with radiological images of real patients by improving knowledge in the radiological and surgical fields. Furthermore, its use can be considered strategic in a pandemic period, since it ensures, through an online platform, the continuation of anatomical and surgical training on dissecting cadavers.