Publications by authors named "Camila Ferreira de Souza"

Article Synopsis
  • Despite improvements in treatment, melanoma still often leads to poor patient outcomes, and there is a lack of effective biological models to study its progression.
  • Researchers analyzed the gene expression profiles of various melanoma cell lines representing different stages of the disease, finding distinct gene expression patterns linked to cell differentiation and mesenchymal transitions.
  • The study identified several genes that could serve as prognostic markers for melanoma progression, enhancing our understanding of the disease and suggesting potential new drug targets.
View Article and Find Full Text PDF

Glioma diagnosis is based on histomorphology and grading; however, such classification does not have predictive clinical outcome after glioblastomas have developed. To date, no bona fide biomarkers that significantly translate into a survival benefit to glioblastoma patients have been identified. We previously reported that the IDH mutant G-CIMP-high subtype would be a predecessor to the G-CIMP-low subtype.

View Article and Find Full Text PDF

The analysis of gene expression patterns in cancers has improved the understanding of the mechanisms underlying the process of metastatic progression. However, the acquisition of invasive behavior in melanoma is poorly understood. In melanoma, components of the immune system can contribute to tumor progression, and inflammatory cells can influence almost all aspects of cancer progression, including metastasis.

View Article and Find Full Text PDF

Background: Metastatic melanoma is a highly aggressive skin cancer and currently resistant to systemic therapy. Melanomas may involve genetic, epigenetic and metabolic abnormalities. Evidence is emerging that epigenetic changes might play a significant role in tumor cell plasticity and metastatic phenotype of melanoma cells.

View Article and Find Full Text PDF

Melanoma is a human neurocristopathy associated with developmental defects in the neural crest-derived epidermal melanocytes. At the present time, at least three hypotheses were identified that may explain melanoma aetiology, as follows: (1) a model of linear progression from differentiated melanocytes to metastatic cancer cells (2) a model involving the appearance of melanoma stem-like cells, and (3) an epigenetic progenitor model of cancer. Treating metastatic melanoma is one of the most serious challenges in the 21st century.

View Article and Find Full Text PDF