María Sol Brassesco

Prof. Dr. María Sol Brassesco

orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

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

Representative Publications

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27 July 2010 in Genes, Chromosomes and Cancer
Verified
Journal Article
Closed access
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MCMaria Angelica Cortez
Maria Angelica Cortez
MNMilena Sabrina Nicoloso
Milena Sabrina Nicoloso
MSMasayoshi Shimizu
Masayoshi Shimizu
SRSimona Rossi
Simona Rossi
GGGopal Gopisetty
Gopal Gopisetty
George CalinGeorge Calin
George Calin

1 March 2012 in Leukemia Research
Verified
Journal Article
Closed access
Jaqueline Carvalho de OliveiraJaqueline Carvalho de Oliveira
Jaqueline Carvalho de Oliveira
CSCarlos Alberto Scrideli
Carlos Alberto Scrideli
MBMaría Sol Brassesco
María Sol Brassesco
AMAndressa Gois Morales
Andressa Gois Morales
JPJulia Pezuk
Julia Pezuk
LTLuiz Gonzaga Tone
Luiz Gonzaga Tone

26 July 2013 in Cancer Gene Therapy
Verified
Journal Article
Open access
PDF file
JPJulia Pezuk
Julia Pezuk
MBMaría Sol Brassesco
María Sol Brassesco
AMA G Morales
A G Morales
Jaqueline Carvalho de OliveiraJaqueline Carvalho de Oliveira
Jaqueline Carvalho de Oliveira
RQR G de Paula Queiroz
R G de Paula Queiroz
LTLuiz Gonzaga Tone
Luiz Gonzaga Tone
Glioblastoma (GBM) is one of the most aggressive central nervous system tumors with a patient’s median survival of <1 year. Polo-like kinases (PLKs) are a family of serine/threonine kinases that have key roles in cell cycle control and DNA-damage response. We evaluated PLK1, 2, 3 and 4 gene expression in 8 GBM cell lines and 17 tumor samples, and analyzed the effect of the PLK1 inhibition on SF188 and T98G GBM cell lines and 13 primary cultures. Our data showed PLK1 overexpression and a variable altered expression of PLK2, 3 and 4 genes in GBM tumor samples and cell lines. Treatments with nanomolar concentrations of BI 2536, BI 6727, GW843682X or GSK461364 caused a significant decrease in GBM cells proliferation. Colony formation was also found to be inhibited (P<0.05), whereas apoptosis rate and mitotic index were significantly increased (P<0.05) after PLK1 inhibition in both GBM cell lines. Cell cycle analysis showed an arrest at G2 (P<0.05) and cell invasion was also decreased after PLK1 inhibition. Furthermore, simultaneous combinations of BI 2536 and temozolomide produced synergistic effects for both the cell lines after 48 h of treatment. Our findings suggest that PLK1 might be a promising target for the treatment of GBMs.

6 June 2012 in Child's Nervous System
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Journal Article
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MSMarcelo Volpon Santos
Marcelo Volpon Santos
Luciano FurlanettiLuciano Furlanetti
Luciano Furlanetti
Elvis Terci ValeraElvis Terci Valera
Elvis Terci Valera
MBMaría Sol Brassesco
María Sol Brassesco
LTLuiz Gonzaga Tone
Luiz Gonzaga Tone
RORicardo Santos de Oliveira
Ricardo Santos de Oliveira

9 December 2011 in Journal of Cancer Research and Clinical Oncology
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Journal Article
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KBKleiton Silva Borges
Kleiton Silva Borges
ACAngel Maurício Castro-Gamero
Angel Maurício Castro-Gamero
DMDaniel Antunes Moreno
Daniel Antunes Moreno
VSVanessa da Silva Silveira
Vanessa da Silva Silveira
MBMaría Sol Brassesco
María Sol Brassesco
LTLuiz Gonzaga Tone
Luiz Gonzaga Tone

1 January 2011 in Genetics and Molecular Biology
Verified
Journal Article
Open access
PDF file
KBKleiton Silva Borges
Kleiton Silva Borges
MBMaría Sol Brassesco
María Sol Brassesco
CSCarlos Alberto Scrideli
Carlos Alberto Scrideli
ASAdemilson Espencer Egea Soares
Ademilson Espencer Egea Soares
LTLuiz Gonzaga Tone
Luiz Gonzaga Tone
Propolis is a resin formed by a complex chemical composition of substances that bees collect from plants. Since ancient times, propolis has been used in folk medicine, due to its biological properties, that include antimicrobial, anti-inflammatory, antitumoral and immunomodulatory activities. Glioblastoma is the most common human brain tumor. Despite the improvements in GBM standard treatment, patients’ prognosis is still very poor. The aim of this work was to evaluate in vitro the Tubi-bee propolis effects on human glioblastoma (U251 and U343) and fibroblast (MRC-5) cell lines. Proliferation, clonogenic capacity and apoptosis were analyzed after treatment with 1 mg/mL and 2 mg/mL propolis concentrations for different time periods. Additionally, glioblastoma cell lines were submitted to treatment with propolis combined with temozolomide (TMZ). Data showed an antiproliferative effect of tubi-bee propolis against glioblastoma and fibroblast cell lines. Combination of propolis with TMZ had a synergic anti-proliferative effect. Moreover, propolis caused decrease in colony formation in glioblastoma cell lines. Propolis treatment had no effects on apoptosis, demonstrating a cytostatic action. Further investigations are needed to elucidate the molecular mechanism of the antitumor effect of propolis, and the study of its individual components may reveal specific molecules with antiproliferative capacity.