Scientific Reports · 2023 · 15 citations · 23 references
MedicineMolecular GeneticsOncologyCancer GeneticsMolecular OncologyTumor MicroenvironmentCancer BiomarkersCancer GenomicsCancer ImmunotherapyImmuno-oncology BiomarkersMutational SignaturesT Cell Responses To TumorsBreast Cancer GenomicsImmune Microenvironment PrognosisMutational Signature PrognosticsTertiary Lymphoid StructuresTp53 MutationsTumor Cell ProliferationTumor Mutational BurdenTumor Mutational Burden Assessment
Tertiary lymphoid structures (TLSs) play a crucial role in determining prognosis and response to immunotherapy in several solid malignancies. Nevertheless, the effect of TLS-associated gene signature based on The Cancer Genome Atlas (TCGA) cohort in patients with breast cancer (BRCA) remains controversial. Based on TCGA-BRCA dataset (n = 866), 9-gene was identified to construct an TLS signature and further analyzed its prognostic value. Then, we explored the relationship of this TLS signature with molecular subtype, immune microenvironment, tumor mutational burden (TMB). High-TLS signature patients had a better overall survival (OS) than low-TLS signature patients, consistent with the results in the METABRIC cohort. Multivariate analysis revealed that TLS signature remained an independent prognostic indicator for OS. In addition, we established a nomogram with the integration of TLS signature and other independent variables to predict individual risk of death. The comprehensive results showed that patients with high TLS signature benefit from immunotherapy; the signature was also correlated with inhibition of cell proliferation pathways, low TP53 mutation rate, high infiltration of B cells, CD8 + T cells, CD4 + T cells, and M1 macrophages. Therefore, TLS signature is a promising biomarker to distinguish the prognosis and immune microenvironment in BRCA.
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Rebecca L. Siegel, Kimberly D. Miller, Hannah E. Fuchs et al. · CA A Cancer Journal for Clinicians · 2022 · 18.2K citations · Full text
KEGG for taxonomy-based analysis of pathways and genomes
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The genomic and transcriptomic architecture of 2,000 breast tumours reveals novel subgroups
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