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New therapeutic proposal for cancer: combination of mitogen with a cell stress pathway inhibitor.

Grant number: 24/09407-0
Support Opportunities:Scholarships in Brazil - Post-Doctoral
Start date: August 01, 2024
End date: June 30, 2026
Field of knowledge:Biological Sciences - Biochemistry - Molecular Biology
Principal Investigator:Hugo Aguirre Armelin
Grantee:Thompson Eusébio Pavan Torres
Host Institution: Instituto Butantan. Secretaria da Saúde (São Paulo - Estado). São Paulo , SP, Brazil
Associated research grant:13/07467-1 - CeTICS - Center of Toxins, Immune-Response and Cell Signaling, AP.CEPID

Abstract

This research project aims to explore a novel therapeutic approach to cancer proposed by Dias and colleagues in 2019 and 2024, Torres and colleagues (in preparation) and the patent number BR 10 2024 006319-8. The central proposal states that malignant cells, unlike normal cells, undergo cell death when exposed to a specific combination of a mitogen and a defined stress pathway inhibitor. This pathophysiological difference between normal and malignant cells provides a unique therapeutic opportunity. Our results have demonstrated that in vitro combinations of FGF-2 (mitogen) + Bortezomib (a clinically used proteasome inhibitor) and LB-100 (a mitogen-like, inhibitor of phosphatase PP2A/PP5) + Bortezomib synergistically induce tumor cell death without harming normal cells. Furthermore, in vivo, these combinations inhibit tumor growth and metastasis without toxicity in xenograft models (human triple-negative breast cancer cell line, MDA-MB-231) and in orthotopic models (murine triple-negative breast cancer cell line, 4T1). The continuation of these studies will explore the applicability of this approach across different types of malignant cell lines (prostate triple-negative, glioblastoma, liver cancer, etc.) in xenograft models, identifying their specific vulnerabilities to mitogenic activation. By exploring stress response pathways after mitogenic activation, we seek to innovate in cancer therapy.

News published in Agência FAPESP Newsletter about the scholarship:
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