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Splicing signature database development to delineate cancer pathways using literature mining and transcriptome machine learningopen access

Authors
Lee, KyubinHyung, DaejinCho, Soo YoungYu, NamheeHong, SewhaKim, JihyunKim, SunshinHan, Ji-YounPark, Charny
Issue Date
Mar-2023
Publisher
Research Network of Computational and Structural Biotechnology
Keywords
Machine -learning; Alternative splicing; Tumor transcriptome; Database; Gene signature
Citation
Computational and Structural Biotechnology Journal, v.21, pp 1978 - 1988
Pages
11
Indexed
SCIE
SCOPUS
Journal Title
Computational and Structural Biotechnology Journal
Volume
21
Start Page
1978
End Page
1988
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/112553
DOI
10.1016/j.csbj.2023.02.052
ISSN
2001-0370
Abstract
Alternative splicing (AS) events modulate certain pathways and phenotypic plasticity in cancer. Although previous studies have computationally analyzed splicing events, it is still a challenge to uncover biological functions induced by reliable AS events from tremendous candidates. To provide essential splicing event signatures to assess pathway regulation, we developed a database by collecting two datasets: (i) reported literature and (ii) cancer transcriptome profile. The former includes knowledge-based splicing signatures collected from 63,229 PubMed abstracts using natural language processing, extracted for 202 pathways. The latter is the machine learning-based splicing signatures identified from pan-cancer transcriptome for 16 cancer types and 42 pathways. We established six different learning models to classify pathway activities from splicing profiles as a learning dataset. Top-ranked AS events by learning model feature importance became the signature for each pathway. To validate our learning results, we performed evaluations by (i) performance metrics, (ii) differential AS sets acquired from external datasets, and (iii) our knowledge-based signatures. The area under the receiver operating characteristic values of the learning models did not exhibit any drastic difference. However, random-forest distinctly presented the best performance to compare with the AS sets identified from external datasets and our knowledge-based signatures. Therefore, we used the signatures obtained from the random-forest model. Our database provided the clinical characteristics of the AS signatures, including survival test, molecular subtype, and tumor microenvironment. The regulation by splicing factors was additionally investigated. Our database for developed signatures supported retrieval and visualization system.(c) 2023 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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ERICA 과학기술융합대학 (ERICA 의약생명과학과)
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