4.7 Article

A multiple network-based bioinformatics pipeline for the study of molecular mechanisms in oncological diseases for personalized medicine

期刊

BRIEFINGS IN BIOINFORMATICS
卷 22, 期 6, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/bib/bbab180

关键词

colorectal cancer; personalized medicine; pipeline workflow; biological-biomedical networks

资金

  1. ELIXIR IT research infrastructure project
  2. project RARE.PLAT.NET [CUP B63D18000380007, SURF 17061BP000000012]
  3. project Combattare la resistenza tumorale: piattaforma integrata multidisciplinare per un approccio tecnologico alle oncoterapie [CUP B61G18000470007, SURF 17061BP000000010]
  4. University of Salerno, Fondi di Ateneo per la Ricerca di base [ORSA170308, ORSA180380, ORSA199808, ORSA177994, ORSA181753,, ORSA197335]
  5. Italian Ministry of University and Research [2017483NH8]

向作者/读者索取更多资源

The study focuses on improving cancer diagnostics through multiple network analysis and predicts the impact of gene mutations on human diseases using biological networks. Results demonstrate that the bioinformatics pipeline based on a multiple network approach can effectively identify molecular changes in cancer patients and determine the most suitable drug treatment for individual patients.
Motivation: Assessment of genetic mutations is an essential element in the modern era of personalized cancer treatment. Our strategy is focused on 'multiple network analysis' in which we try to improve cancer diagnostics by using biological networks. Genetic alterations in some important hubs or in driver genes such as BRAF and TP53 play a critical role in regulating many important molecular processes. Most of the studies are focused on the analysis of the effects of single mutations, while tumors often carry mutations of multiple driver genes. The aim of this work is to define an innovative bioinformatics pipeline focused on the design and analysis of networks (such as biomedical and molecular networks), in order to: (1) improve the disease diagnosis; (2) identify the patients that could better respond to a given drug treatment; and (3) predict what are the primary and secondary effects of gene mutations involved in human diseases. Results: By using our pipeline based on a multiple network approach, it has been possible to demonstrate and validate what are the joint effects and changes of the molecular profile that occur in patients with metastatic colorectal carcinoma (mCRC) carrying mutations in multiple genes. In this way, we can identify the most suitable drugs for the therapy for the individual patient. This information is useful to improve precision medicine in cancer patients. As an application of our pipeline, the clinically significant case studies of a cohort of mCRC patients with the BRAF V600E-TP53 I195N missense combined mutation were considered.

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