Lung adenocarcinoma (LUAD) is the most important subtype of lung cancer. It is well known that the gut microbiome plays an important role in the pathophysiology of various diseases, including cancer, but little research has been done on the intestinal microbiome associated with LUAD. Utilizing bioinformatics tools and data analysis, we identified novel potential prognostic biomarkers for LUAD.
View Article and Find Full Text PDFEquitable and accessible education in life sciences, bioengineering, and synthetic biology is crucial for training the next generation of scientists, fostering transparency in public decision-making, and ensuring biotechnology can benefit a wide-ranging population. As a groundbreaking technology for genome engineering, CRISPR has transformed research and therapeutics. However, hands-on exposure to this technology in educational settings remains limited due to the extensive resources required for CRISPR experiments.
View Article and Find Full Text PDFTissue-resident memory T cells (T) are a specialized subset of long-lived memory T cells that reside in peripheral tissues. However, the impact of T-related immunosurveillance on the tumor-immune microenvironment (TIME) and tumor progression across various non-small-cell lung cancer (NSCLC) patient populations is yet to be elucidated. Our comprehensive analysis of multiple independent single-cell and bulk RNA-seq datasets of patient NSCLC samples generated reliable, unique T signatures, through which we inferred the abundance of T in NSCLC.
View Article and Find Full Text PDFCancer immunotherapy represents a paradigm shift in oncology, offering a superior anti-tumor efficacy and the potential for durable remission. The success of personalized vaccines and cell therapies hinges on the identification of immunogenic epitopes capable of eliciting an effective immune response. Current limitations in the availability of immunogenic epitopes restrict the broader application of such therapies.
View Article and Find Full Text PDFTissue-resident memory T cells (T) are a specialized T cell population residing in peripheral tissues. The presence and potential impact of T in the tumor immune microenvironment (TIME) remain to be elucidated. Here, we systematically investigated the relationship between T and melanoma TIME based on multiple clinical single-cell RNA-seq datasets and developed signatures indicative of T infiltration.
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