Abstract B026: Modulation of signalling cross-talk between pJNK and pAKT generates optimal apoptotic response

Abstract Tumor necrosis factor alpha (TNFα) is a well-known modulator of apoptosis by maintaining a balance between proliferation and cell-death in normal cells. Cancer cells often evade apoptotic response following TNFα stimulation by altering signaling cross- talks. Thus, varying the extent of signaling cross-talk could enable optimal TNFα mediated apoptotic dynamics. Herein, we use an experimental data-driven mathematical modeling to quantitate the extent of synergistic signaling cross-talk between the intracellular entities phosphorylated JNK (pJNK) and phosphorylated AKT (pAKT) that orchestrate the phenotypic apoptosis level by modulating the activated Caspase3 dynamics. Our study reveals that this modulation is orchestrated by the distinct dynamic nature of the synergism at early and late phases. We show that this synergism in signal flow is governed by branches originating from either TNFα receptor and NFκB, which facilitates signaling through survival pathways. We demonstrate that the experimentally quantified apoptosis levels semi-quantitatively correlates with the model simulated Caspase3 transients. Interestingly, perturbing pJNK and pAKT transient dynamics fine-tunes this accumulated Caspase3 guided apoptotic response. Thus, our study offers useful insights for identifying potential targeted therapies for optimal apoptotic response. Citation Format: Baishakhi Tikader, Sharmila Biswas, Sandip Kar, Ganesh A. Viswanathan. Modulation of signalling cross-talk between pJNK and pAKT generates optimal apoptotic response [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Tumor Immunology and Immunotherapy; 2024 Oct 18-21; Boston, MA. Philadelphia (PA): AACR; Cancer Immunol Res 2024;12(10 Suppl):Abstract nr B026.

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Journal
Cancer Immunology Research
Published
2024-10-18
DOI
https://doi.org/10.1158/2326-6074.tumimm24-b026
Primary Topic
Phagocytosis and Immune Regulation
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article
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article

Abstract B026: Modulation of signalling cross-talk between pJNK and pAKT generates optimal apoptotic response

Baishakhi Tikader, Ganesh A. Viswanathan, Sharmila Biswas, Sandip Kar
Cancer Immunology Research
Phagocytosis and Immune Regulation
article

Abstract B026: Modulation of signalling cross-talk between pJNK and pAKT generates optimal apoptotic response

Baishakhi Tikader, Ganesh A. Viswanathan, Sharmila Biswas, Sandip Kar
article en

Abstract

Abstract Tumor necrosis factor alpha (TNFα) is a well-known modulator of apoptosis by maintaining a balance between proliferation and cell-death in normal cells. Cancer cells often evade apoptotic response following TNFα stimulation by altering signaling cross- talks. Thus, varying the extent of signaling cross-talk could enable optimal TNFα mediated apoptotic dynamics. Herein, we use an experimental data-driven mathematical modeling to quantitate the extent of synergistic signaling cross-talk between the intracellular entities phosphorylated JNK (pJNK) and phosphorylated AKT (pAKT) that orchestrate the phenotypic apoptosis level by modulating the activated Caspase3 dynamics. Our study reveals that this modulation is orchestrated by the distinct dynamic nature of the synergism at early and late phases. We show that this synergism in signal flow is governed by branches originating from either TNFα receptor and NFκB, which facilitates signaling through survival pathways. We demonstrate that the experimentally quantified apoptosis levels semi-quantitatively correlates with the model simulated Caspase3 transients. Interestingly, perturbing pJNK and pAKT transient dynamics fine-tunes this accumulated Caspase3 guided apoptotic response. Thus, our study offers useful insights for identifying potential targeted therapies for optimal apoptotic response. Citation Format: Baishakhi Tikader, Sharmila Biswas, Sandip Kar, Ganesh A. Viswanathan. Modulation of signalling cross-talk between pJNK and pAKT generates optimal apoptotic response [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Tumor Immunology and Immunotherapy; 2024 Oct 18-21; Boston, MA. Philadelphia (PA): AACR; Cancer Immunol Res 2024;12(10 Suppl):Abstract nr B026.

Cancer Immunology ResearchVol. 12(10_Supplement)
Indian Institute of Technology Bombay (IN), Indian Institute of Science Bangalore (IN)
Openalex Percentile: Top 77%
Phagocytosis and Immune Regulation
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