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Omics · study · 2026

Molecular architecture of the tumor microenvironment caused by BRCA1 and BRCA2 somatic mutations in human lung adenocarcinoma

Listed in NCBI GEO

We have employed a single cell sequencing approach using 10x Genomics scRNAseq and scTCR-seq to study the heterogeneity and molecular architecture of tumor microenvironment (TME) caused by BRCA1 and BRCA2 somatic mutations in lung adenocarcinoma (LUAD).

Description

LUADs are considered to be a heterogeneity population in the lung epithelium. Homologous recombination repair (HRR) deficiency has been linked to enhanced immunotherapy responses in non-small cell lung cancer patients.

The HRR genes BRCA1 and BRCA2 are key regulators of DNA repair, yet their impact on the TME in LUAD remains unclear.This study provides a comprehensive characterization of the BRCA-mutant TME in LUAD patients, uncovering distinct immune response mechanisms and potential therapeutic strategies. These findings enhance our understanding of BRCA1/2-driven molecular architecture and offer novel insights into improving therapy efficacy in LUAD.

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From keywords
Life Sciences
Inferred from text
Cancer 75% · Genetics 72% · Sequencing 75%
Provenance · 1 source records, 11 field assertions
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NCBI GEOGSE29270014 d agoJSON v1
FieldAssertionExtractorEvidence
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concepts[modality].local:modality:sequencingenrichment · NCBI GEOkeyword-concept-rules@1.0.0title+description (75%)
concepts[organism].NCBITaxon:9606source · NCBI GEOconnector:ncbi_geo@1.0.0/taxon
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