Peptidomics-Driven Strategy Reveals Peptides and Predicted Proteases Associated With Oral Cancer Prognosis

Leandro Xavier Neves(Brazilian Biosciences National Laboratory), Daniela C. Granato(Brazilian Biosciences National Laboratory), Ariane F. Busso‐Lopes(Brazilian Biosciences National Laboratory), Carolina Moretto Carnielli(Brazilian Biosciences National Laboratory), Fábio Malta de Sá Patroni(Universidade Estadual de Campinas (UNICAMP)), Tatiane De Rossi(Brazilian Biosciences National Laboratory), Ana K. Oliveira(Brazilian Biosciences National Laboratory), Ana Carolina Prado Ribeiro(Instituto do Câncer do Estado de São Paulo), Thaís Bianca Brandão(Instituto do Câncer do Estado de São Paulo), André Nimtz Rodrigues(Faculdade de Medicina de Jundiaí), Pammela A. Lacerda(Faculdade de Medicina de Jundiaí), Miyuki Uno, Nilva K. Cervigne(Faculdade de Medicina de Jundiaí), Alan Roger Santos‐Silva(Universidade Estadual de Campinas (UNICAMP)), Luiz Paulo Kowalski(Universidade de São Paulo), Márcio Ajudarte Lopes(Universidade Estadual de Campinas (UNICAMP)), Adriana Franco Paes Leme(Brazilian Biosciences National Laboratory)
Molecular & Cellular Proteomics
November 11, 2020
Cited by 30Open Access
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Abstract

Protease activity has been associated with pathological processes that can lead to cancer development and progression. However, understanding the pathological unbalance in proteolysis is challenging because changes can occur simultaneously at protease, their inhibitor, and substrate levels. Here, we present a pipeline that combines peptidomics, proteomics, and peptidase predictions for studying proteolytic events in the saliva of 79 patients and their association with oral squamous cell carcinoma (OSCC) prognosis. Our findings revealed differences in the saliva peptidome of patients with (pN+) or without (pN0) lymph-node metastasis and delivered a panel of ten endogenous peptides correlated with poor prognostic factors plus five molecules able to classify pN0 and pN+ patients (area under the receiver operating characteristic curve > 0.85). In addition, endopeptidases and exopeptidases putatively implicated in the processing of differential peptides were investigated using cancer tissue gene expression data from public repositories, reinforcing their association with poorer survival rates and prognosis in oral cancer. The dynamics of the OSCC-related proteolysis were further explored via the proteomic profiling of saliva. This revealed that peptidase/endopeptidase inhibitors exhibited reduced levels in the saliva of pN+ patients, as confirmed by selected reaction monitoring-mass spectrometry, while minor changes were detected in the level of saliva proteases. Taken together, our results indicated that proteolytic activity is accentuated in the saliva of patients with OSCC and lymph-node metastasis and, at least in part, is modulated by reduced levels of salivary peptidase inhibitors. Therefore, this integrated pipeline provided better comprehension and discovery of molecular features with implications in the oral cancer metastasis prognosis.


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