Role of the protein RECK in HPV-mediated cell transformation

• Grant number: 17/02997-3
• Support Opportunities: Regular Research Grants
• Duration: June 01, 2017 - May 31, 2019
• Field of knowledge: Biological Sciences - Biochemistry - Molecular Biology
• Principal Investigator: Enrique Mario Boccardo Pierulivo
• Grantee: Enrique Mario Boccardo Pierulivo
• Host Institution: Instituto de Ciências Biomédicas (ICB). Universidade de São Paulo (USP). São Paulo , SP, Brazil
• Associated researchers: Ana Paula Lepique

Abstract

Some HPV types, known as high-risk HPVs, are etiologically associated with almost all the cases of cervical cancer and mora than 50% or other genital carcinomas. High-risk HPVs express two oncoproteins, E6 e E7, that act on specific cellular factors promoting sustained cell proliferation, resistance to apoptosis, resistance to cytokines, immune evasion and numeric and structural chromosomal alterations. Besides, it was observed that alterations in components of the extracellular matrix (ECM), for instance the matrix metalloproteinases (MMPs) and some of their regulators, are among the mechanisms of carcinogenesis associated with HPV infection. MMPs are responsible for MEC remodeling and their up-regulation exerts a key role in several processes. Previous studies from our laboratory have shown that cells expressing HPV17 E7 oncoprotein exhibit increased MMP-9 expression levels and activity. Moreover, E7 expression is associated to the down-regulation of MMPs regulators TIMP-2 and RECK. The RECK (reversion inducing cysteine rich protein with kazal motifs) protein plays and essential function in tissue remodeling and tumor angiogenesis through the post-transcriptional regulation of MMP-2, MMP-9 and MMP-14 (MT1-MMP) activity. Furthermore, we showed that RECK expression is down-regulated in high-grade cervical lesions and cervical cancer samples when compared with cervicitis samples. Altogether, these data suggest that negative RECK regulation may constitute an important step in the natural history of cervical cancer. This study aims to determine the role of RECK in HPV-mediated carcinogenesis. To achieve this goal we will analyze the effect of RECK superexpression in the tumorigenic potential of cervical cnacer derived cell lines both in vitro and in vivo. Besides, we will analyze the effect of HPV proteins in the control of the transcriptional activity of RECK promoter. Our results will contribute to identify the role of RECK in HPV-associated tumors onset and progression. (AU)

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)

HERBSTER, SUELLEN; TROMBETTA-LIMA, MARINA; DE SOUZA-SANTOS, PAULO THIAGO; PALADINO, ANDRESSA; SILVEIRA, CAIO RAONY FARINA; SOGAYAR, MARI CLEIDE; VILLA, LUISA LINA; LEPIQUE, ANA PAULA; BOCCARDO, ENRIQUE. Low RECK Expression Is Part of the Cervical Carcinogenesis Mechanisms. CANCERS, v. 13, n. 9, MAY 2021. (08/57889-1, 17/02997-3, 10/20002-0, 13/27006-9)

CARRILLO-BELTRAN, DIEGO; MUNOZ, JUAN P.; GUERRERO-VASQUEZ, NAHIR; BLANCO, RANCES; LEON, OSCAR; DE SOUZA LINO, VANESCA; TAPIA, JULIO C.; MALDONADO, EDIO; DUBOIS-CAMACHO, KAREN; HERMOSO, MARCELA A.; et al. Human Papillomavirus 16 E7 Promotes EGFR/PI3K/AKT1/NRF2 Signaling Pathway Contributing to PIR/NF-kappa B Activation in Oral Cancer Cells. CANCERS, v. 12, n. 7, JUL 2020. (17/02997-3, 10/20002-0)

NUNES, EMILY MONTOSA; TALPE-NUNES, VALERIA; SOBRINHO, JOAO SIMAO; FERREIRA, SILVANEIDE; LINO, VANESCA DE SOUZA; TERMINI, LARA; FERNANDES SILVA, GABRIELA AVILA; BOCCARDO, ENRIQUE; VILLA, LUISA LINA; SICHERO, LAURA. E6/E7 Functional Differences among Two Natural Human Papillomavirus 18 Variants in Human Keratinocytes. Viruses-Basel, v. 13, n. 6, JUN 2021. (15/26346-6, 15/26345-0, 17/02997-3)