Evidence map›Paper›PMID 27897000›Full record

ArticlePacific Symposium on Biocomputing. Pacific Symposium on Biocomputing2017

IDENTIFYING CANCER SPECIFIC METABOLIC SIGNATURES USING CONSTRAINT-BASED MODELS.

A Schultz, S Mehta, C W Hu, F W Hoff, T M Horton, S M Kornblau, A A Qutub

Abstract readValidation Study
In one paragraph

Article in Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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

7 authors.

A SchultzDepartment of Bioengineering, Rice University, Houston, Texas 77005, U.S.A.
S Mehta
C W Hu
F W Hoff
T M Horton
S M Kornblau
A A Qutub

Funding

Identifying Cell Stress Proteins that Predict Clinical Response in Pediatric AMLR01CA164024 · NCI · BAYLOR COLLEGE OF MEDICINE · PI HORTON, TERZAH M · 2013 to 2017
$1.7M
Spatially-delineated System-level Analyses and Control of Cytoskeletal RegulationR01GM106027 · NIGMS · RICE UNIVERSITY · PI BALAZSI, GABOR, DIEHL, MICHAEL R · 2013 to 2016
$1.2M
NCI NIH HHS R01 CA164024NIGMS NIH HHS R01 GM106027
6 · The paper itself

Abstract

Cancer metabolism differs remarkably from the metabolism of healthy surrounding tissues, and it is extremely heterogeneous across cancer types. While these metabolic differences provide promising avenues for cancer treatments, much work remains to be done in understanding how metabolism is rewired in malignant tissues. To that end, constraint-based models provide a powerful computational tool for the study of metabolism at the genome scale. To generate meaningful predictions, however, these generalized human models must first be tailored for specific cell or tissue sub-types. Here we first present two improved algorithms for (1) the generation of these context-specific metabolic models based on omics data, and (2) Monte-Carlo sampling of the metabolic model ux space. By applying these methods to generate and analyze context-specific metabolic models of diverse solid cancer cell line data, and primary leukemia pediatric patient biopsies, we demonstrate how the methodology presented in this study can generate insights into the rewiring differences across solid tumors and blood cancers.

Indexed as

Models, BiologicalAlgorithmsCell Line, TumorChildComputational BiologyHumansLeukemiaMetabolic Networks and PathwaysMonte Carlo MethodNeoplasmsProteomics

Identifiers

PMID27897000
PMCPMC5173378

What OpenQuestion holds

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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.