Publications by authors named "Maria-Fernanda Senosain"

Background: Lung cancer is the leading cause of cancer death worldwide, with poor survival despite recent therapeutic advances. A better understanding of the complexity of the tumor microenvironment is needed to improve patients' outcome.

Methods: We applied a computational immunology approach (involving immune cell proportion estimation by deconvolution, transcription factor activity inference, pathways and immune scores estimations) in order to characterize bulk transcriptomics of 62 primary lung adenocarcinoma (LUAD) samples from patients across disease stages.

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Article Synopsis
  • The study investigates the differences in immune gene expression and survival outcomes between HER2-low and HER2-zero breast cancers, focusing on the tumor immune microenvironment (TME).
  • Comprehensive genomic analysis was conducted on samples from 129 patients with advanced HER2-negative breast cancer, assessing immune-related gene expressions and their correlation with patient survival rates.
  • Results indicate that while there were no significant differences in immune gene expression between HER2-low and HER2-zero cancers, patients with HER2-low tumors exhibited a higher rate of estrogen receptor positivity and significantly better overall survival.
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KEYNOTE-522 resulted in FDA approval of the immune checkpoint inhibitor pembrolizumab in combination with neoadjuvant chemotherapy for patients with early-stage, high-risk, triple-negative breast cancer (TNBC). Unfortunately, pembrolizumab is associated with several immune-related adverse events (irAEs). We aimed to identify potential tumor microenvironment (TME) biomarkers which could predict patients who may attain pathological complete response (pCR) with chemotherapy alone and be spared the use of anti-PD-1 immunotherapy.

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Background: Cancer-testis antigens (CTAs) are tumor antigens that are normally expressed in the testes but are aberrantly expressed in several cancers. CTA overexpression drives the metastasis and progression of lung cancer, and is associated with poor prognosis. To improve lung cancer diagnosis, prognostic prediction, and drug discovery, robust CTA identification and quantitation is needed.

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Lung adenocarcinoma (LUAD) is the predominant type of lung cancer in the U.S. and exhibits a broad variety of behaviors ranging from indolent to aggressive.

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Article Synopsis
  • - Lung adenocarcinoma (LUAD) is a common and aggressive form of lung cancer, with its recurrence risk poorly understood, leading researchers to explore the role of immune response in tumor growth as a factor affecting patient outcomes.
  • - The study analyzed immune cell density in tumors from 100 LUAD patients (stages I and II), using advanced techniques to assess T-cell and mast cell presence in relation to recurrence-free survival (RFS).
  • - Findings indicate that higher densities of T-cells and mast cells in tumors are associated with significantly reduced recurrence risk, emphasizing the potential role of the immune environment in cancer prognosis, though further research is needed due to the small sample size.
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Unlabelled: Lung adenocarcinoma (LUAD) is a heterogeneous group of tumors associated with different survival rates, even when detected at an early stage. Here, we aim to investigate the biological determinants of early LUAD indolence or aggressiveness using radiomics as a surrogate of behavior. We present a set of 92 patients with LUAD with data collected across different methodologies.

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Modern technologies designed for tissue structure visualization like brightfield microscopy, fluorescent microscopy, mass cytometry imaging (MCI) and mass spectrometry imaging (MSI) provide large amounts of quantitative and spatial information about cells and tissue structures like vessels, bronchioles etc. Many published reports have demonstrated that the structural features of cells and extracellular matrix (ECM) and their interactions strongly predict disease development and progression. Computational image analysis methods in combination with spatial analysis and machine learning can reveal novel structural patterns in normal and diseased tissue.

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Lung adenocarcinoma (ADC) is a heterogeneous group of tumors associated with different survival rates, even when detected at an early stage. Here, we aim to investigate whether CyTOF identifies cellular and molecular predictors of tumor behavior. We developed and validated a CyTOF panel of 34 antibodies in four ADC cell lines and PBMC.

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Lung cancer is one of the deadliest diseases in the world and is the leading cause of cancer-related deaths. Among the histological types, adenocarcinoma is the most common, and it is characterized by a high degree of heterogeneity at many levels including clinical, behavioral, cellular and molecular. While most lung cancers are known for their aggressive behavior, up to 18.

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We have a limited understanding of the molecular underpinnings of early adenocarcinoma (ADC) progression. We hypothesized that the behavior of early ADC can be predicted based on genomic determinants. To identify genomic alterations associated with resected indolent and aggressive early lung ADCs.

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