» Articles » PMID: 38761803

Subtype-WGME Enables Whole-genome-wide Multi-omics Cancer Subtyping

Overview
Specialty Cell Biology
Date 2024 May 18
PMID 38761803
Authors
Affiliations
Soon will be listed here.
Abstract

We present an innovative strategy for integrating whole-genome-wide multi-omics data, which facilitates adaptive amalgamation by leveraging hidden layer features derived from high-dimensional omics data through a multi-task encoder. Empirical evaluations on eight benchmark cancer datasets substantiated that our proposed framework outstripped the comparative algorithms in cancer subtyping, delivering superior subtyping outcomes. Building upon these subtyping results, we establish a robust pipeline for identifying whole-genome-wide biomarkers, unearthing 195 significant biomarkers. Furthermore, we conduct an exhaustive analysis to assess the importance of each omic and non-coding region features at the whole-genome-wide level during cancer subtyping. Our investigation shows that both omics and non-coding region features substantially impact cancer development and survival prognosis. This study emphasizes the potential and practical implications of integrating genome-wide data in cancer research, demonstrating the potency of comprehensive genomic characterization. Additionally, our findings offer insightful perspectives for multi-omics analysis employing deep learning methodologies.

References
1.
El-Ashmawy N, Hussien F, El-Feky O, Hamouda S, Al-Ashmawy G . Serum LncRNA-ATB and FAM83H-AS1 as diagnostic/prognostic non-invasive biomarkers for breast cancer. Life Sci. 2020; 259:118193. DOI: 10.1016/j.lfs.2020.118193. View

2.
Yan L, Wu X, Zhang Y, Tan Q, Xu J, Wang Y . LncRNA ENST00000370438 promotes cell proliferation by upregulating DHCR24 in breast cancer. Mol Carcinog. 2023; 62(6):855-865. DOI: 10.1002/mc.23529. View

3.
Nguyen H, Shrestha S, Draghici S, Nguyen T . PINSPlus: a tool for tumor subtype discovery in integrated genomic data. Bioinformatics. 2018; 35(16):2843-2846. DOI: 10.1093/bioinformatics/bty1049. View

4.
Toth R, Schiffmann H, Hube-Magg C, Buscheck F, Hoflmayer D, Weidemann S . Random forest-based modelling to detect biomarkers for prostate cancer progression. Clin Epigenetics. 2019; 11(1):148. PMC: 6805338. DOI: 10.1186/s13148-019-0736-8. View

5.
Elliott K, Larsson E . Non-coding driver mutations in human cancer. Nat Rev Cancer. 2021; 21(8):500-509. DOI: 10.1038/s41568-021-00371-z. View