Overview
Genomic medicine in cancer is the clinical application of high-throughput sequencing and molecular profiling to characterize the genetic and genomic alterations of an individual tumor and to guide diagnosis, prognosis, and treatment. Rather than classifying malignancies by tissue of origin alone, it interrogates the somatic mutations, copy-number changes, gene fusions, and expression patterns that drive oncogenesis, enabling therapy matched to a tumor's molecular characteristics. Core concepts include distinguishing driver from passenger mutations, mapping the mutational landscape of recurrently altered genes such as the tumor suppressor TP53, and identifying actionable targets for precision therapeutics. Profiling spans DNA, RNA, and protein layers and supports the development and validation of biomarkers for risk stratification, treatment selection, and monitoring of response and resistance. Multigene assays exemplify how expression signatures inform clinical decisions, as in estrogen-receptor-positive breast cancer where recurrence scores estimate prognosis and chemotherapy benefit. Genomic approaches also illuminate the contributions of inherited versus sporadic alterations, somatic signaling perturbations, and oncogenic viral associations to tumor development. Allied immunogenomic methods extend this framework to the tumor-immune interface, supporting immunomonitoring and immunotherapy selection. Together these strategies advance individualized cancer care while raising methodological priorities in assay standardization, data interpretation, and the translation of molecular findings into validated clinical practice.
Research published in this journal
7 peer-reviewed articles, ranked by relevance. Each links to its DOI.
Molecular and Cell Biological Considerations in the Initiation and Development of Sporadic Non-Hereditary Solid Cancers
Correlation of Oncotype DX Recurrence Score with the Expression of Insulin Receptor Substrate Proteins in Estrogen Receptor + Breast Cancer
The Current Immunoassays and Emerging Immunogenomic Approaches for Immunomonitoring Cancer and Infectious Diseases
High-Throughput Complex Disease Modeling for Ethical Drug Discovery: Clinical Relevance of a NAM Platform for Cancer Biomarker Development
The Identification of Somatic Mutations in Interferon-G Signal Molecules in Human Uterine Leiomyosarcoma
Association of Epstein-Barr Virus with Gastric Carcinoma among Sudanese Patients
How this research is being cited
The 7 articles above have been cited 24 times in the scholarly literature. Citation data via OpenAlex and Crossref, updated Jun 2026.
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2026 · Biomedical & Pharmacology Journal
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2026 · Genes
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2025 · Open Journal of Genetics
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2023 · Cells
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2023 · Cells
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2023 · Research Square (Research Square)
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CFTR-mediated monocyte/macrophage dysfunction revealed by cystic fibrosis proband-parent comparisons2022 · JCI Insight
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CFTR-mediated monocyte/macrophage dysfunction revealed by cystic fibrosis proband-parent comparisons2022 · JCI Insight
A sample of recent works citing this journal's research on Genomic Medicine in Cancer, linking to each citing work.