Skip to content

Mathematical Modeling Highlights the Complex Role of AKT in TRAIL-Induced Apoptosis of Colorectal Carcinoma Cells

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)182-193
Number of pages36
JournaliScience
Volume12
Early online date14 Jan 2019
DOIs
DateAccepted/In press - 8 Jan 2019
DateE-pub ahead of print - 14 Jan 2019
DatePublished (current) - 22 Feb 2019

Abstract

Protein kinase B/AKT is a highly connected protein involved in a range of signaling pathways. Although it is known to regulate several proteins in the apoptotic pathway, its system level effects remain poorly understood. We investigated the dynamic interactions between AKT and key apoptotic proteins, and constructed a deterministic Ordinary Differential Equation protein interaction model of extrinsic apoptosis. Incorporating AKT and its indirect inhibitor, PTEN, this was used to generate predictions of system dynamics. Using eigenanalysis, we identified AKT and cytochrome c as the protein species most sensitive to perturbations. Cell death assays in Type II HCT116 colorectal carcinoma cells revealed a tendency towards Type I cell death behavior in the XIAP-/- background, with cells displaying accelerated TRAIL-induced apoptosis. Finally, AKT inhibition experiments implicated AKT and not PTEN in influencing apoptotic proteins during early phases of TRAIL-induced apoptosis.

Additional information

Copyright © 2019 The Author(s). Published by Elsevier Inc. All rights reserved.

    Research areas

  • Cancer, Cell Biology, In Silico Biology

Download statistics

No data available

Documents

Documents

  • Full-text PDF (final published version)

    Rights statement: This is the final published version of the article (version of record). It first appeared online via Elsevier at https://www.sciencedirect.com/science/article/pii/S258900421930015X?via%3Dihub. Please refer to any applicable terms of use of the publisher.

    Final published version, 3.76 MB, PDF document

    Licence: CC BY

DOI

View research connections

Related faculties, schools or groups