INTEGRATION OF HIGH-THROUGHPUT OMICS METHODS IN PENILE CANCER CELL CULTURES

• Grant number: 15/25373-0
• Support type: Scholarships abroad - Research Internship - Post-doctor
• Effective date (Start): April 08, 2016
• Effective date (End): April 07, 2017
• Field of knowledge: Health Sciences - Medicine - Pathological Anatomy and Clinical Pathology
• Principal researcher: Silvia Regina Rogatto
• Grantee: Hellen Kuasne
• Supervisor abroad: Jan Baumbach
• Home Institution: Faculdade de Medicina (FMB). Universidade Estadual Paulista (UNESP). Campus de Botucatu. Botucatu , SP, Brazil
• Research place: University of Southern Denmark (SDU), Denmark
• Associated to the scholarship: 13/03667-6 - Functional study in penis carcimomas for the validation of candidate molecular markers obtained from integrated global analyzes (genomics, transcriptomics and DNA methylation), BP.PD

Abstract

Penile carcinoma (PeCa) is a frequent disease in poor and developing countries showing high morbidity. Despite of the progress in the molecular research of PeCa, including very recently published high-throughput studies conducted by our group, the lack of well characterized in vitro models precludes new advances in the knowledge of cellular processes as well as in preclinical tests for anticancer drugs efficacy. During the post-doctoral period, we established and characterized six cell cultures derived from penile carcinomas aiming to provide reliable in vitro models for functional and pre-clinical studies in PeCa. The objective of this BEPE internship is to perform high-throughput methods to molecularly characterize these cell cultures. Since multiple mechanisms can modify gene expression and promote carcinogenesis, a multidimensional integrative analysis will be performed for a more comprehensive understanding of the signaling pathways that contribute to penile tumorigenesis. Transcriptomic and translatomic (HTA 2.0 Affymetrix), genomic (Cytoscan-Affymetrix), epigenomic (Infinium® Human Methylation450 BeadChip) and proteomic (Reverse phase protein array - RPPA) approaches will be performed in the six PeCa cell cultures and two foreskin cell lines. Integration of all omics profiles and interactome analysis will be performed in collaboration with Dr Jan Baumbach, University of Southern Denmark, DK. In addition, the data herein obtained will be compared with results previously obtained by our group in PeCa fresh tissues. From these analyses, we intend to reveal altered pathways in PeCa that could be used to develop targeted treatments. In addition, we also aim to investigate the potential of these cell models to be used in preclinical trials of PeCa.

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)

KUASNE, HELLEN; CANTO, LUISA MATOS DO; AAGAARD, MADS MALIK; MUNOZ, JUAN JOSE MOYANO; JAMBLINNE, CAMILLE DE; MARCHI, FABIO ALBUQUERQUE; SCAPULATEMPO-NETO, CRISTOVAM; FARIA, ELINEY FERREIRA; LOPES, ADEMAR; CARRENO, SEBASTIEN; ROGATTO, SILVIA REGINA. Penile Cancer-Derived Cells Molecularly Characterized as Models to Guide Targeted Therapies. CELLS, v. 10, n. 4 APR 2021. Web of Science Citations: 0.