A graph-based multi-sample test for identifying pathways associated with cancer progression. (August 2020)

• Record Type: Journal Article
• Authors: Zhang, Qingyang; Mahdi, Ghadeer; Tinker, Jian; Chen, Hao
• Is Part Of: Computational biology and chemistry. Volume 87(2020)
• Publication Date: 2020-08
• Subjects: TCGA The Cancer Genome Atlas -- MST minimum spanning tree -- CNV copy number variation -- BH Benjamini-Hochberg -- MDS multidimensional scaling -- BN Bayesian network; Edge-count test -- Tumorigenesis -- Serous ovarian cancer -- Pathway analysis -- The Cancer Genome Atlas; Chemistry -- Data processing -- Periodicals; Biology -- Data processing -- Periodicals; Biochemistry -- Data processing; Biology -- Data processing; Molecular biology -- Data processing; Periodicals; Electronic journals; 542.85
• DOI: 10.1016/j.compbiolchem.2020.107285
• Languages: English
• ISSNs: 1476-9271

Abstract

Graphical abstract: Highlights: We develop a new approach to testing pathway dynamics over cancer progression. The proposed method is based on a novel graph-based multivariate test. We found several KEGG pathways that contribute to ovarian cancer progression. Abstract: Cancer is in general not a result of an abnormality of a single gene but a consequence of changes in many genes, it is therefore of great importance to understand the roles of different oncogenic and tumor suppressor pathways in tumorigenesis. In recent years, there have been many computational models developed to study the genetic alterations of different pathways in the evolutionary process of cancer. However, most of the methods are knowledge-based enrichment analyses and inflexible to analyze user-defined pathways or gene sets. In this paper, we develop a nonparametric and data-driven approach to testing for the dynamic changes of pathways over the cancer progression. Our method is based on an expansion and refinement of the pathway being studied, followed by a graph-based multivariate test, which is very easy to implement in practice. The new test is applied to the rich Cancer Genome Atlas data to study the (epi)genetic alterations of 186 KEGG pathways in the development of serous ovarian cancer. To make use of the comprehensive data, we incorporate three data types in the analysis representing gene expression level, copy number and DNA methylation level. Our analysis suggests a list of nine pathways that are closely associated with serous ovarian cancer progression, including cell cycle, ERBB, JAK-STAT signaling and p53 signaling pathways. By pairwise tests, we found that most of the identified pathways contribute only to a particular transition step. For instance, the cell cycle and ERBB pathways play key roles in the early-stage transition, while the ECM receptor and apoptosis pathways contribute to the progression from stage III to stage IV. The proposed computational pipeline is powerful in detecting important pathways and gene sets that drive cancers at certain stage(s). It offers new insights into the understanding of molecular mechanism of cancer initiation and progression.