Advanced search
Start date
Betweenand

Vasohibin aptamer (VASH-aptamer): a potential theranostic agent in colorectal cancer

Grant number: 19/23592-7
Support Opportunities:Regular Research Grants
Start date: March 01, 2021
End date: February 28, 2022
Field of knowledge:Health Sciences - Medicine - Surgery
Agreement: Carleton University
Mobility Program: SPRINT - Projetos de pesquisa - Mobilidade
Principal Investigator:Denise Gonçalves Priolli
Grantee:Denise Gonçalves Priolli
Principal researcher abroad: Maria C DeRosa
Institution abroad: Carleton University, Canada
Host Institution: Universidade São Francisco (USF). Campus Bragança Paulista. Bragança Paulista , SP, Brazil
Associated researchers:Thalita Rocha
Associated research grant:18/21471-5 - VASOHIBIN: POTENTIAL TARGETING INHIBITOR OF ANGIOGENESIS IN COLORECTAL CANCER, AP.R

Abstract

Angiogenesis is a term that describes blood vessels formation, a physiological process involved in growth and healing, which is also linked to the development of diseases, including cancer, its progression and metastasis development. Differently, tumor angiogenesis is characterized by the neovessels formation through the stimulation and proliferation of preexisting endothelial vessel cells and thus is called neo-angiogenesis. Among the most recently described angiogenesis regulators are vasohibins (VASHs). The vasohibin family is composed of two members: vasohibin-1 (VASH-1), which is expressed in vessels and in colorectal cancer and is prognostic-related, and vasohibin-2 (VASH-2), its homolog, which is expressed in the tumor tissue and seems to have a stimulatory effect on angiogenesis. Currently, antiangiogenic therapy is an option, especially in cancer advanced stages, but their side effects are still broad, due to their action in tumor endothelium and in normal endothelium. In addition, drug resistance development has been a problem. The specific target identification, such as VASH, arouses interest in antiangiogenic therapy. The project was divided into three distinct phases. In phase I (Brazil) the aim was to understand the VASH behavior in colorectal cancer (CCR) carcinogenesis from biopsies of human normal tissue, adenoma and adenocarcinoma; in phase II (Brazil) a new antiangiogenic agent has been studied in an animal model of human colon cancer, while in phase III we intend to develop an aptamer of VASH as a theranostic agent in colon cancer (Canada). (AU)

Articles published in Agência FAPESP Newsletter about the research grant:
More itemsLess items
Articles published in other media outlets ( ):
More itemsLess items
VEICULO: TITULO (DATA)
VEICULO: TITULO (DATA)

Scientific publications
(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)
PELOSI, ANDREA; FERNANDES, ANNA MARIA A. P. C.; MACIEL, LEONARDO; SILVA, ALEX A. R.; MENDES, GIULIA F.; BUENO, LUISA F. G.; SILVA, LIVIA MARIA F. M.; BREDARIOL, RAFAEL G.; SANTANA, MAYCON; PORCARI, ANDREIA; et al. Liquid chromatography coupled to high-resolution mass spectrometry metabolomics: A useful tool for investigating tumor secretome based on a three-dimensional co-culture model. PLoS One, v. 17, n. 9, p. 8-pg., . (19/04314-6, 18/21471-5, 19/23592-7, 18/21906-1)
KRAEMER, MAURICIO BEITIA; SILVA, KAREN CHRISTINE; KRAEMER, CAMILA CUNHA FRANCA; PEREIRA, JULIANA SILVA; DOS REIS, IVAN GUSTAVO MASSELI; PRIOLLI, DENISE GONCALVES; MESSIAS, LEONARDO HENRIQUE DALCHECO. Validity of the peak velocity to detect physical training improvements in athymic mice. FRONTIERS IN PHYSIOLOGY, v. 13, p. 11-pg., . (19/23592-7, 18/21471-5)