LION LBD: a literature-based discovery system for cancer biology
Open accessAbstract
Motivation: The overwhelming size and rapid growth of the biomedical literature make it impossible for scientists to read all studies related to their work, potentially leading to missed connections and wasted time and resources. Literature-based discovery (LBD) aims to alleviate these issues by identifying implicit links between disjoint parts of the literature. While LBD has been studied in depth since its introduction three decades ago, there has been limited work making use of recent advances in biomedical text processing methods in LBD. Results: We present LION LBD, a literature-based discovery system that enables researchers to navigate published information and supports hypothesis generation and testing. The system is built with a particular focus on the molecular biology of cancer using state-of-the-art machine learning and natural language processing methods, including named entity recognition and grounding to domain ontologies covering a wide range of entity types and a novel approach to detecting references to the hallmarks of cancer in text. LION LBD implements a broad selection of co-occurrence based metrics for analyzing the strength of entity associations, and its design allows real-time search to discover indirect associations between entities in a database of tens of millions of publications while preserving the ability of users to explore each mention in its original context in the literature. Evaluations of the system demonstrate its ability to identify undiscovered links and rank relevant concepts highly among potential connections. Availability and implementation: The LION LBD system is available via a web-based user interface and a programmable API, and all components of the system are made available under open licenses from the project home page http://lbd.lionproject.net. Supplementary information: Supplementary data are available at Bioinformatics online.
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Existing LBD methods and tools primarily quantify the strength of association without assessing relevance to or support of a specific scientific hypothesis.
“However, while existing LBD methods can efficiently identify statistically significant associations between biomedical terms, they generally lack a structured framework for evaluating whether these discovered associations meaningfully support or contradict a specific scientific hypothesis.”
From SKiM-GPT: combining biomedical literature-based discovery with large language model hypothesis evaluation (2025) · cites this paper as [27]
Section 3.3 describes LBD scores based on co-occurrence and statistical association, and Section 4.3 says the system can suggest unverifiable or causally invalid connections. These passages support the concern that association scores alone do not establish meaningful support for a hypothesis. The paper does not establish the broader claim that existing LBD methods generally lack a structured framework for assessing whether evidence supports or contradicts a specific hypothesis; its Introduction also describes closed discovery as hypothesis testing. (LLM, conf=0.82)
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- Authors
- Pyysalo, S., Baker, S., Ali, I., Haselwimmer, S., Shah, T., Young, A., Guo, Y., Högberg, J., Stenius, U., Narita, M., & Korhonen, A.
- Affiliations
- University of Cambridge (GB)
- Karolinska Institutet (SE)
- Corresponding author
- Pyysalo, Sampo
- ORCID
- Venue
- Bioinformatics
- Publisher
- Oxford University Press (OUP)
- Published
- 2018-10-09
- Volume
- 35
- Issue
- 9
- Pages
- 1553-1561
- ISSN
- 1367-4803 (ISSN-L)
- 1367-4811
- PMC
- PMC6499247
- OpenAlex
- W2896730986
- Cited by
- 65
- References
- 2
- Citations by year
- 2026: 1 · 2025: 8 · 2024: 10 · 2023: 11 · 2022: 7 · 2021: 7 · 2020: 10 · 2019: 11
- FWCI
- 2.49
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Bioinformatics (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Apollo (University of Cambridge) (submittedVersion, cc-by)
- Apollo (cc-by)
- Funders
- Research Councils UK (MR/M013049/1)
- Cancer Research UK Cambridge Institute Core (C14303/A17197)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Biomedical Text Mining and Ontologies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Physical Sciences › Computer Science › Artificial Intelligence › Advanced Text Analysis Techniques
- Keywords
- literature-based discovery, tumor biology, biomedical text mining, named entity recognition, ontology grounding, cancer hallmarks, entity association, hypothesis generation
- MeSH terms
- Algorithms, Humans, Natural Language Processing, Neoplasms, Publications, Databases, Factual
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