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Updated: Mar 12, 2026

Author Spotlight: Unveiling the Role of TMOD3 in Platinum Resistance and Immune Infiltration in Ovarian Cancer
Published on: August 2, 2024
InFlo: a novel systems biology framework identifies cAMP-CREB1 axis as a key modulator of platinum resistance in
N Dimitrova1, A B Nagaraj2, A Razi2
1Department of Clinical Informatics Solutions and Services, Philips Research North America, Briarcliff Manor, NY, USA.
Abstract:
Characterizing the complex interplay of cellular processes in cancer would enable the discovery of key mechanisms underlying its development and progression. Published approaches to decipher driver mechanisms do not explicitly model tissue-specific changes in pathway networks and the regulatory disruptions related to genomic aberrations in cancers. We therefore developed InFlo, a novel systems biology approach for characterizing complex biological processes using a unique multidimensional framework integrating transcriptomic, genomic and/or epigenomic profiles for any given cancer sample. We show that InFlo robustly characterizes tissue-specific differences in activities of signalling networks on a genome scale using unique probabilistic models of molecular interactions on a per-sample basis. Using large-scale multi-omics cancer datasets, we show that InFlo exhibits higher sensitivity and specificity in detecting pathway networks associated with specific disease states when compared to published pathway network modelling approaches. Furthermore, InFlo's ability to infer the activity of unmeasured signalling network components was also validated using orthogonal gene expression signatures. We then evaluated multi-omics profiles of primary high-grade serous ovarian cancer tumours (N=357) to delineate mechanisms underlying resistance to frontline platinum-based chemotherapy. InFlo was the only algorithm to identify hyperactivation of the cAMP-CREB1 axis as a key mechanism associated with resistance to platinum-based therapy, a finding that we subsequently experimentally validated. We confirmed that inhibition of CREB1 phosphorylation potently sensitized resistant cells to platinum therapy and was effective in killing ovarian cancer stem cells that contribute to both platinum-resistance and tumour recurrence. Thus, we propose InFlo to be a scalable and widely applicable and robust integrative network modelling framework for the discovery of evidence-based biomarkers and therapeutic targets.
Insights
InFlo, a new systems biology tool, identifies cancer
Area of Science:
- Cancer Biology
- Systems Biology
- Genomics
Background:
- Understanding cancer requires characterizing complex cellular interactions.
- Existing methods lack tissue-specific pathway network modeling for genomic aberrations.
- This gap hinders the discovery of cancer development and progression mechanisms.
Purpose of the Study:
- To develop a novel systems biology approach, InFlo, for characterizing complex biological processes.
- To integrate multi-omics data (transcriptomic, genomic, epigenomic) for cancer sample analysis.
- To identify tissue-specific pathway network disruptions and therapeutic targets.
Main Methods:
- Developed InFlo, a multidimensional framework integrating multi-omics data.
- Utilized probabilistic models for per-sample molecular interaction analysis.
- Applied InFlo to large-scale multi-omics cancer datasets and ovarian cancer tumors.
Main Results:
- InFlo robustly identifies tissue-specific signaling network activities.
- InFlo demonstrates superior sensitivity and specificity compared to existing pathway modeling approaches.
- Identified cAMP-CREB1 axis hyperactivation as a key mechanism of platinum resistance in ovarian cancer.
Conclusions:
- InFlo is a scalable, robust integrative network modeling framework.
- InFlo facilitates the discovery of evidence-based biomarkers and therapeutic targets.
- Inhibition of CREB1 phosphorylation sensitizes resistant ovarian cancer cells and targets cancer stem cells.
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