Cell-free DNA promotes malignant transformation in non-tumor cells
Autor: | Ana Carolina Laus, Leandro M. Colli, Natássia Caroline Resende Corrêa, Patrícia Tieme Fujimura, Luiz Ricardo Goulart, Carolina Hassibe Thomé, Luciane Sussuchi da Silva, Victor Alexandre Felix Bastos, Leticia Ferro Leal, Rui Manuel Reis, Aline Gomes de Souza, Karina Marangoni, Vivian Alonso Goulart, Izabella C C Ferreira, Paula de Souza Santos, Mário Machado Martins |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
Male
Cell biology Molecular biology Urology Science Cell Gene Expression Article Metastasis Malignant transformation Circulating Tumor DNA Prostate cancer SANGUE Cell Movement Cell Line Tumor microRNA medicine Humans Gene Cancer Multidisciplinary biology Chemistry CD44 Tryptophan Prostatic Neoplasms Cell migration medicine.disease Gene Expression Regulation Neoplastic MicroRNAs medicine.anatomical_structure Cell Transformation Neoplastic Hyaluronan Receptors Matrix Metalloproteinase 9 Oncology biology.protein Cancer research Disease Progression Medicine |
Zdroj: | Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020) Scientific Reports Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual) Universidade de São Paulo (USP) instacron:USP |
ISSN: | 2045-2322 |
Popis: | Cell-free DNA is present in different biological fluids and when released by tumor cells may contribute to pro-tumor events such as malignant transformation of cells adjacent to the tumor and metastasis. Thus, this study analyzed the effect of tumor cell-free DNA, isolated from the blood of prostate cancer patients, on non-tumor prostate cell lines (RWPE-1 and PNT-2). To achieve this, we performed cell-free DNA quantification and characterization assays, evaluation of gene and miRNA expression profiling focused on cancer progression and EMT, and metabolomics by mass spectrometry and cellular migration. The results showed that tumor-free cell DNA was able to alter the gene expression of MMP9 and CD44, alter the expression profile of nine miRNAs, and increased the tryptophan consumption and cell migration rates in non-tumor cells. Therefore, tumor cell-free DNA was capable of altering the receptor cell phenotype, triggering events related to malignant transformation in these cells, and can thus be considered a potential target for cancer diagnosis and therapy. |
Databáze: | OpenAIRE |
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