Evidence map›Paper›PMID 21062161›Full record

ReviewFuture oncology (London, England)2010

Integrative genomic approaches in cervical cancer: implications for molecular pathogenesis.

Gopeshwar Narayan, Vundavalli V Murty

Open access · greenAbstract readReview
In one paragraph

Review in Future oncology (London, England), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

30 citing papers in PubMed, 52 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Journal of Cancer · 2022
    Article
  11. Aberrant methylation-mediated downregulation of lncRNAJournal of biological research (Thessalonike, Greece) · 2020
    Article
  12. Article
  13. Research progress on KIF3B and related diseases.Annals of translational medicine · 2019
    Review
  14. Article
  15. CAS (CSE1L) signaling pathway in tumor progression and its potential as a biomarker and target for targeted therapy.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

2 authors at 1 institution in 2 countries.

Gopeshwar NarayanDepartment of Pathology & Cell Biology, Institute for Cancer Genetics, Columbia University Medical Center, 1130 St. Nicholas Avenue, New York, NY, USA.
Vundavalli V Murty
Cancer Genetics (United States) · US

Funding

Molecular Genetics of Cervical Cancer ProgressionR21CA095647 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI VUNDAVALLI, MURTY V V S · 2003 to 2004
$393k
NCI NIH HHS CA095647NCI NIH HHS R21 CA095647
6 · The paper itself

Abstract

Cervical cancer (CC) as a single diagnostic entity exhibits differences in clinical behavior and poor outcomes in response to therapy in advanced tumors. Although infection of high-risk human papillomavirus is recognized as an important initiating event in cervical tumorigenesis, stratification of CC into subclasses for progression and response to treatment remains elusive. Existing knowledge of genetic, epigenetic and transcriptional alterations is inadequate in addressing the issues of diagnosis, progression and response to treatment. Recent technological advances in high-throughput genomics and the application of integrative approaches have greatly accelerated gene discovery, facilitating the identification of molecular targets. In this article, we discuss the results obtained by preliminary integrative analysis of DNA copy number increases and gene expression, utilizing the two most common copy number-gained regions of 5p and 20q in identifying gene targets in CC. These analyses provide insights into the roles of genes such as RNASEN, POLS and SKP2 on 5p, KIF3B, RALY and E2F1 at 20q11.2 and CSE1L, ZNF313 and B4GALT5 at 20q13.13. Future integrative applications using additional datasets, such as mutations, DNA methylation and clinical outcomes, will raise the promise of accomplishing the identification of biological pathways and molecular targets for therapies for patients with CC.

Indexed as

Epigenesis, GeneticFemaleGene DosageGene Expression ProfilingGenomicsHumansUterine Cervical Neoplasms

Identifiers

PMID21062161
PMCPMC3037979
OpenAlexW2110015050

What OpenQuestion holds

Textmetadata
LicenceTDM
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.