Evidence map›Paper›PMID 31671657›Full record

ReviewGenes2019

The Many Faces of Gene Regulation in Cancer: A Computational Oncogenomics Outlook.

Enrique Hernández-Lemus, Helena Reyes-Gopar, Jesús Espinal-Enríquez, Soledad Ochoa

Abstract readReview
In one paragraph

Review in Genes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Review
  2. Loss of long-range co-expression is a common feature in cancer.NPJ systems biology and applications · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Potential Drug Synergy Through the ERBB2 Pathway in HER2+ Breast Tumors.International journal of molecular sciences · 2024
    Article
  7. Review
  8. Article
  9. Onco-Breastomics: An Eco-Evo-Devo Holistic Approach.International journal of molecular sciences · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Multi-Omics Model Applied to Cancer Genetics.International journal of molecular sciences · 2021
    Review
  16. Modularity in Biological Networks.Frontiers in genetics · 2021
    Review
  17. Computational and structural biotechnology journal · 2021
    Article
  18. Article
  19. Review
  20. On a Class of Tensor Markov Fields.Entropy (Basel, Switzerland) · 2020
    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.

Enrique Hernández-LemusComputational Genomics Division, National Institute of Genomic Medicine, Mexico City 14610, Mexico. ehernandez@inmegen.gob.mx.ORCID 0000-0002-1872-1397
Helena Reyes-GoparComputational Genomics Division, National Institute of Genomic Medicine, Mexico City 14610, Mexico. hreyes.gopar@gmail.com.
Jesús Espinal-EnríquezComputational Genomics Division, National Institute of Genomic Medicine, Mexico City 14610, Mexico. jespinal@inmegen.gob.mx.
Soledad OchoaComputational Genomics Division, National Institute of Genomic Medicine, Mexico City 14610, Mexico. mochoa@inmegen.edu.mx.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is a complex disease at many different levels. The molecular phenomenology of cancer is also quite rich. The mutational and genomic origins of cancer and their downstream effects on processes such as the reprogramming of the gene regulatory control and the molecular pathways depending on such control have been recognized as central to the characterization of the disease. More important though is the understanding of their causes, prognosis, and therapeutics. There is a multitude of factors associated with anomalous control of gene expression in cancer. Many of these factors are now amenable to be studied comprehensively by means of experiments based on diverse omic technologies. However, characterizing each dimension of the phenomenon individually has proven to fall short in presenting a clear picture of expression regulation as a whole. In this review article, we discuss some of the more relevant factors affecting gene expression control both, under normal conditions and in tumor settings. We describe the different omic approaches that we can use as well as the computational genomic analysis needed to track down these factors. Then we present theoretical and computational frameworks developed to integrate the amount of diverse information provided by such single-omic analyses. We contextualize this within a systems biology-based multi-omic regulation setting, aimed at better understanding the complex interplay of gene expression deregulation in cancer.

Indexed as

Computational BiologyGene Expression Regulation, NeoplasticGenomicsHumansMetabolomicsNeoplasmsProteomicsSystems Biologycomputational oncogenomicsgene expression regulationintegrative biologymulti-omics

Identifiers

PMID31671657
PMCPMC6896122

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Registered trials

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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.