Evidence map›Paper›PMID 19625303›Full record

ArticleJournal of the Royal Society, Interface2010

Systems-level cancer gene identification from protein interaction network topology applied to melanogenesis-related functional genomics data.

Tijana Milenkovic, Vesna Memisevic, Anand K Ganesan, Natasa Przulj

Abstract readEvaluation Study
In one paragraph

Article in Journal of the Royal Society, Interface, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Large-scale analysis of disease pathways in the human interactome.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2018
    Article
  7. Article
  8. Article
  9. PROSNET: INTEGRATING HOMOLOGY WITH MOLECULAR NETWORKS FOR PROTEIN FUNCTION PREDICTION.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2017
    Article
  10. Article
  11. Article
  12. The post-genomic era of biological network alignment.EURASIP journal on bioinformatics & systems biology · 2015
    Article
  13. Article
  14. Article
  15. Article
  16. Fair evaluation of global network aligners.Algorithms for molecular biology : AMB · 2015
    Article
  17. Article
  18. Article
  19. Article
  20. Protein-protein interaction networks (PPI) and complex diseases.Gastroenterology and hepatology from bed to bench · 2014
    Review
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

4 authors.

Tijana MilenkovicDepartment of Computer Science, University of California, Irvine, CA 92697-3435, USA.
Vesna Memisevic
Anand K Ganesan
Natasa Przulj

Funding

Uncover Strategies Used By Biological SystemsP50GM076516 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI CALOF, ANNE LEIGHTON · 2007 to 2016
$25.1M
Aldehyde dehydrogenase: A novel regulator of melanin biogenesisK08AR056001 · NIAMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI GANESAN, ANAND K · 2009 to 2013
$551k
Dissecting the Impact of Autophagy Regulators on Melanogenesis in Normal Human CeR03AR057150 · NIAMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI GANESAN, ANAND K · 2009 to 2011
$203k
NIAMS NIH HHS K08 AR056001NIAMS NIH HHS R03 AR057150NIGMS NIH HHS P50 GM076516
6 · The paper itself

Abstract

Many real-world phenomena have been described in terms of large networks. Networks have been invaluable models for the understanding of biological systems. Since proteins carry out most biological processes, we focus on analysing protein-protein interaction (PPI) networks. Proteins interact to perform a function. Thus, PPI networks reflect the interconnected nature of biological processes and analysing their structural properties could provide insights into biological function and disease. We have already demonstrated, by using a sensitive graph theoretic method for comparing topologies of node neighbourhoods called 'graphlet degree signatures', that proteins with similar surroundings in PPI networks tend to perform the same functions. Here, we explore whether the involvement of genes in cancer suggests the similarity of their topological 'signatures' as well. By applying a series of clustering methods to proteins' topological signature similarities, we demonstrate that the obtained clusters are significantly enriched with cancer genes. We apply this methodology to identify novel cancer gene candidates, validating 80 per cent of our predictions in the literature. We also validate predictions biologically by identifying cancer-related negative regulators of melanogenesis identified in our siRNA screen. This is encouraging, since we have done this solely from PPI network topology. We provide clear evidence that PPI network structure around cancer genes is different from the structure around non-cancer genes. Understanding the underlying principles of this phenomenon is an open question, with a potential for increasing our understanding of complex diseases.

Indexed as

Genes, NeoplasmCluster AnalysisGenomicsHumansMelaninsModels, GeneticNeoplasmsProtein Interaction MappingMelanins

Identifiers

PMID19625303
PMCPMC2842789

What OpenQuestion holds

Textmetadata
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.