Evidence map›Paper›PMID 20015360›Full record

ArticleBMC systems biology2009

Human synthetic lethal inference as potential anti-cancer target gene detection.

Nuria Conde-Pueyo, Andreea Munteanu, Ricard V Solé, Carlos Rodríguez-Caso

Abstract read
In one paragraph

Article in BMC systems biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Causal relationships of inflammatory cytokines and serum metabolites with colorectal carcinoma: A Mendelian randomization study.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2026
    Article
  2. Review
  3. Review
  4. Overcoming selection bias in synthetic lethality prediction.Bioinformatics (Oxford, England) · 2022
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Precision Oncology: The Road Ahead.Trends in molecular medicine · 2017
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
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  17. Article
  18. Article
  19. Article
  20. Proposal for a new therapy for drug-resistant malaria using Plasmodium synthetic lethality inference.International journal for parasitology. Drugs and drug resistance · 2013
    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

4 authors.

Nuria Conde-PueyoICREA-Complex Systems Lab, Universitat Pompeu Fabra, Parc de Recerca Biomedica de Barcelona, Dr Aiguader 88, E-08003 Barcelona, Spain. nuria.conde@upf.edu
Andreea Munteanu
Ricard V Solé
Carlos Rodríguez-Caso

Funding

NCI NIH HHS CA 113004
6 · The paper itself

Abstract

backgroundTwo genes are called synthetic lethal (SL) if mutation of either alone is not lethal, but mutation of both leads to death or a significant decrease in organism's fitness. The detection of SL gene pairs constitutes a promising alternative for anti-cancer therapy. As cancer cells exhibit a large number of mutations, the identification of these mutated genes' SL partners may provide specific anti-cancer drug candidates, with minor perturbations to the healthy cells. Since existent SL data is mainly restricted to yeast screenings, the road towards human SL candidates is limited to inference methods.

resultsIn the present work, we use phylogenetic analysis and database manipulation (BioGRID for interactions, Ensembl and NCBI for homology, Gene Ontology for GO attributes) in order to reconstruct the phylogenetically-inferred SL gene network for human. In addition, available data on cancer mutated genes (COSMIC and Cancer Gene Census databases) as well as on existent approved drugs (DrugBank database) supports our selection of cancer-therapy candidates.

conclusionsOur work provides a complementary alternative to the current methods for drug discovering and gene target identification in anti-cancer research. Novel SL screening analysis and the use of highly curated databases would contribute to improve the results of this methodology.

Indexed as

Computational BiologyMutationAntineoplastic AgentsDatabases, GeneticDrug DesignGenes, LethalGenes, NeoplasmHumansNeoplasmsPhylogenySaccharomyces cerevisiaeAntineoplastic Agents

Identifiers

PMID20015360
PMCPMC2804737

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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.