Evidence map›Paper›PMID 33584816›Full record

ArticleFrontiers in genetics2020

Adverse Drug Reaction Discovery Using a Tumor-Biomarker Knowledge Graph.

Meng Wang, Xinyu Ma, Jingwen Si, Hongjia Tang, Haofen Wang, Tunliang Li, Wen Ouyang, Liying Gong, Yongzhong Tang, Xi He and 2 more

Abstract read
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Article in Frontiers in genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Meng WangSchool of Computer Science and Engineering, Southeast University, Nanjing, China.
Xinyu MaSchool of Computer Science and Engineering, Southeast University, Nanjing, China.
Jingwen SiDepartment of Pharmaceutical Sciences, Tsinghua University, Beijing, China.
Hongjia TangDepartment of Anesthesiology, Third Xiangya Hospital, Central South University, Changsha, China.
Haofen WangCollege of Design and Innovation, Tongji University, Shanghai, China.
Tunliang LiDepartment of Anesthesiology, Third Xiangya Hospital, Central South University, Changsha, China.
Wen OuyangDepartment of Anesthesiology, Third Xiangya Hospital, Central South University, Changsha, China.
Liying GongDepartment of Intensive Care Unit, Third Xiangya Hospital, Central South University, Changsha, China.
Yongzhong TangDepartment of Anesthesiology, Third Xiangya Hospital, Central South University, Changsha, China.
Xi HeDepartment of Anesthesiology, Third Xiangya Hospital, Central South University, Changsha, China.
Wei HuangDepartment of Cardiology, Third Xiangya Hospital, Central South University, Changsha, China.
Xing LiuDepartment of Anesthesiology, Third Xiangya Hospital, Central South University, Changsha, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adverse drug reactions (ADRs) are a major public health concern, and early detection is crucial for drug development and patient safety. Together with the increasing availability of large-scale literature data, machine learning has the potential to predict unknown ADRs from current knowledge. By the machine learning methods, we constructed a Tumor-Biomarker Knowledge Graph (TBKG) which contains four types of node: Tumor, Biomarker, Drug, and ADR using biomedical literatures. Based on this knowledge graph, we not only discovered potential ADRs of antitumor drugs but also provided explanations. Experiments on real-world data show that our model can achieve 0.81 accuracy of three cross-validation and the ADRs discovery of Osimertinib was chosen for the clinical validation. Calculated ADRs of Osimertinib by our model consisted of the known ADRs which were in line with the official manual and some unreported rare ADRs in clinical cases. Results also showed that our model outperformed traditional co-occurrence methods. Moreover, each calculated ADRs were attached with the corresponding paths of "tumor-biomarker-drug" in the knowledge graph which could help to obtain in-depth insights into the underlying mechanisms. In conclusion, the tumor-biomarker knowledge-graph based approach is an explainable method for potential ADRs discovery based on biomarkers and might be valuable to the community working on the emerging field of biomedical literature mining and provide impetus for the mechanism research of ADRs.

Indexed as

adverse drug reactionantitumor drugsbiomarkerexplainable modelknowledge graph

Identifiers

PMID33584816
PMCPMC7873847

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.