Evidence map›Paper›PMID 27819677›Full record

ArticleOncogene2017

InFlo: a novel systems biology framework identifies cAMP-CREB1 axis as a key modulator of platinum resistance in ovarian cancer.

N Dimitrova, A B Nagaraj, A Razi, S Singh, S Kamalakaran, N Banerjee, P Joseph, A Mankovich, P Mittal, A DiFeo and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.0field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

N DimitrovaDepartment of Clinical Informatics Solutions and Services, Philips Research North America, Briarcliff Manor, NY, USA.
A B NagarajCase Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH, USA.
A RaziCase Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH, USA.
S SinghCase Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH, USA.
S KamalakaranDepartment of Clinical Informatics Solutions and Services, Philips Research North America, Briarcliff Manor, NY, USA.
N BanerjeeDepartment of Clinical Informatics Solutions and Services, Philips Research North America, Briarcliff Manor, NY, USA.
P JosephCase Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH, USA.
A MankovichDepartment of Clinical Informatics Solutions and Services, Philips Research North America, Briarcliff Manor, NY, USA.
P MittalDepartment of Electrical Engineering, Princeton University, Princeton, NJ, USA.
A DiFeoCase Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH, USA.
V VaradanCase Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH, USA.
Case Western Reserve University · USPhilips (United States) · USPrinceton University · US

Funding

Targeting 15-PGDH in Colon Cancer Prognosis, Prediction, Treatment and PreventionP50CA150964 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MARKOWITZ, SANFORD D. · 2011 to 2022
$24.6M
TRAINING IN COMPUTATIONAL GENOMIC EPIDEMIOLOGY OF CANCERR25CA094186 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI LI, LI · 2002 to 2016
$6.8M
Computational Genomic Epidemiology of Cancer (CoGEC) Training ProgramT32CA094186 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI Thomas Louis LaFramboise, Rong Xu · 2017 to 2026
$2.6M
NCI NIH HHS P50 CA150964NCI NIH HHS R25 CA094186NCI NIH HHS T32 CA094186
6 · The paper itself

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.

Indexed as

Drug Resistance, NeoplasmCell Line, TumorCyclic AMPCyclic AMP Response Element-Binding ProteinFemaleGene Regulatory NetworksHumansOvarian NeoplasmsSignal TransductionSystems BiologyCREB1 protein, humanCyclic AMPCyclic AMP Response Element-Binding Protein

Identifiers

PMID27819677
PMCPMC5415943
OpenAlexW2554660074

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.