Integrative multi-omics approaches in cancer research: from biological networks to clinical subtypes
Open accessAbstract
Multi-omics approaches are novel frameworks that integrate multiple omics datasets generated from the same patients to better understand the molecular and clinical features of cancers. A wide range of emerging omics and multi-view clustering algorithms now provide unprecedented opportunities to further classify cancers into subtypes, improve the survival prediction and therapeutic outcome of these subtypes, and understand key pathophysiological processes through different molecular layers. In this review, we overview the concept and rationale of multi-omics approaches in cancer research. We also introduce recent advances in the development of multi-omics algorithms and integration methods for multiple-layered datasets from cancer patients. Finally, we summarize the latest findings from large-scale multi-omics studies of various cancers and their implications for patient subtyping and drug development.
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The framework is grounded in a systems biology perspective at the biological level because the diagnostic data it processes reflects the multi-level organization of cancer.
“At the biological level, the diagnostic data it processes reflects the multi-level organization of cancer”
From A generative AI multi-agent framework with integrated XAI governance for cancer diagnostics: from multi-omics interpretation to lifestyle risk stratification (2026) · cites this paper as Heo et al., 2021
The Introduction describes multi-omics data at multiple levels and scales, and the Concluding Remarks say multiple data layers are needed to represent the molecular and clinical structures of cancer patients. These passages support the multi-level view of cancer, but they do not establish what diagnostic data the citing document’s particular framework processes. (LLM, conf=0.82)
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- Authors
- Heo, Y. J., Hwa, C., Lee, G.-H., Park, J.-M., & An, J.-Y.
- Affiliations
- Korea University (KR)
- Venue
- Molecules and Cells
- Publisher
- Elsevier BV
- Published
- 2021-07
- Volume
- 44
- Issue
- 7
- Pages
- 433-443
- ISSN
- 0219-1032 (ISSN-L)
- 1016-8478
- PMC
- PMC8334347
- OpenAlex
- W3180571536
- Cited by
- 294
- References
- 88
- Citations by year
- 2026: 66 · 2025: 81 · 2024: 75 · 2023: 56 · 2022: 15 · 2017: 1
- FWCI
- 3.86
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Molecules and Cells (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- Funders
- National Research Foundation of Korea (2019M3E5D3073568)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer Genomics and Diagnostics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene expression and cancer classification
- Keywords
- multi-omics integration, cancer subtyping, multi-view clustering, biological networks, survival prediction, therapeutic outcome prediction, drug development, cancer genomics
- MeSH terms
- Humans, Neoplasms, Survival Analysis, Computational Biology, Biomedical Research, Metabolomics
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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