Investigator

Patrícia M. A. Silva

Invited Auxiliar Professor of Morfologia e Funções do Corpo Humano · Instituto Universitário de Ciências da Saúde, IUCS-CESPU

About

PMAPatrícia M. A. Si…
Papers(1)
Metformin Impairs Lin…
Collaborators(6)
Ricardo Jorge Dinis-O…Sara RicardoDiana Luísa Almeida-N…Hassan BousbaaJoão P. N. SilvaMariana Nunes
Institutions(3)
Cooperativa De Ensino…Instituto Universitár…Universidade do Porto…

Papers

Metformin Impairs Linsitinib Anti-Tumor Effect on Ovarian Cancer Cell Lines

Ovarian cancer (OC) remains one of the leading causes of cancer-related mortality among women. Targeting the insulin-like growth factor 1 (IGF-1) signaling pathway has emerged as a promising therapeutic strategy. Linsitinib, an IGF-1 receptor (IGF-1R) inhibitor, has shown potential in disrupting this pathway. Additionally, metformin, commonly used in the treatment of type 2 diabetes, has been studied for its anti-cancer properties due to its ability to inhibit metabolic pathways that intersect with IGF-1 signaling, making it a candidate for combination therapy in cancer treatments. This study explores the anti-cancer effects of linsitinib and metformin on OVCAR3 cells by the suppression of the IGF-1 signaling pathway by siRNA-mediated IGF-1 gene silencing. The goal is to evaluate their efficacy as therapeutic agents and to emphasize the critical role of this pathway in OC cell proliferation. Cellular viability was evaluated by resazurin-based assay, and apoptosis was assessed by flux cytometry. The results of this study indicate that the combination of linsitinib and metformin exhibits an antagonistic effect (obtained by SynergyFinder 2.0 Software), reducing their anti-neoplastic efficacy in OC cell lines. Statistical analyses were performed using ordinary one-way or two-way ANOVA, followed by Tukey’s or Šídák’s multiple comparison tests. While linsitinib shows promise as a therapeutic option for OC, further research is needed to identify agents that could synergize with it to enhance its therapeutic efficacy, like the combination with standard chemotherapy in OC (carboplatin and paclitaxel).

159Works
1Papers
6Collaborators
NeoplasmsCell Line, TumorApoptosisMitosisDrug Resistance, NeoplasmOvarian NeoplasmsDrug Screening Assays, Antitumor

Positions

2021–

Invited Auxiliar Professor of Morfologia e Funções do Corpo Humano

Instituto Universitário de Ciências da Saúde · IUCS-CESPU

2017–

Research Technician

Cooperativa de Ensino Superior Politécnico e Universitário (CESPU) · IUCS-CESPU

2011–

Invited Assistant Professor (Cellular and Molecular Biology)

Cooperativa de Ensino Superior Politécnico e Universitário · Department of Sciences

2013–

PhD Student in Biomedical Sciences

University of Algarve/CBMR

2008–

Monitor of Learning Internships I and II (Histochemistry area)

Cooperativa de Ensino Superior Politécnico e Universitário · Pathological, Cytological and Thanatological Anatomy

2011–

High Research technician

Cooperativa de Ensino Superior Politécnico e Universitário

2010–

Histology technician

INEB

2009–

Diagnostic and therapeutic technician

IPATIMUP

Education

2017

PhD in Biomedical Sciences

University of Algarve/CBMR · Ciências Biomédicas e Medicina

2011

Master in Molecular Biology Techniques and Cytomics in Health Sciences

Instituto Politécnico de Saude do Norte Escola Superior de Saúde do Vale do Ave

2008

Pathological, Cytological and Thanatological Anatomy

Instituto Politécnico de Saude do Norte Escola Superior de Saúde do Vale do Sousa

Keywords
Kinetochore-microtubule interactions; Cell division; Spindle assembly checkpoint; Drug screening