Evidence map›Paper›PMID 20851183›Full record

ReviewSeminars in cancer biology2011

Gene signatures in hepatocellular carcinoma (HCC).

Ourania M Andrisani, Leo Studach, Philippe Merle

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in cancer biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

35 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Current Advances in RNA Therapeutics for Human Diseases.International journal of molecular sciences · 2022
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Integrative genomic analysis of mouse and human hepatocellular carcinoma.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  17. Review
  18. MCM2: An alternative to Ki-67 for measuring breast cancer cell proliferation.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2017
    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

3 authors at 2 institutions in 2 countries.

Ourania M AndrisaniBasic Medical Sciences Department and Purdue Center for Cancer Research, Purdue University, West Lafayette, IN 47907, United States. andrisao@purdue.edu
Leo Studach
Philippe Merle
Purdue University West Lafayette · USUniversité Claude Bernard Lyon 1 · FR

Funding

Role of CREB/ATF Proteins in Hepatocyte Growth ControlR01DK044533 · NIDDK · PURDUE UNIVERSITY WEST LAFAYETTE · PI ANDRISANI, OURANIA M. · 1999 to 2021
$5.1M
Role of Polo-like kinase (Plk-1) in Hepatitis B Virus-mediated Hepatocellular CarR21CA135192 · NCI · PURDUE UNIVERSITY · PI ANDRISANI, OURANIA M. · 2009 to 2010
$369k
SOMATOSTATIN GENE EXPRESSION--FUNCTIONAL DOMAINS OF CREBR29DK044533 · NIDDK · PURDUE UNIVERSITY WEST LAFAYETTE · PI ANDRISANI, OURANIA M. · 1993 to 1997
–
NCI NIH HHS CA135192NCI NIH HHS R21 CA135192NIDDK NIH HHS DK044533NIDDK NIH HHS R01 DK044533
6 · The paper itself

Abstract

Primary hepatocellular carcinoma (HCC) is a significant human cancer globally, with poor prognosis. New and efficacious therapy strategies are needed as well as new biomarkers for early detection of at-risk patients. In this review, we discuss select microarray studies of human HCCs, and propose a gene signature that has promise for clinical/translational application. This gene signature combines the proliferation cluster of genes and the hepatic cancer initiating/stem cell gene cluster for identification of HCCs with poor prognosis. Evidence from cell-based assays identifies the existence of a mechanistic link between these two gene clusters, involving the proliferation cluster gene polo-like kinase 1 (PLK1). We propose that PLK1 is a promising therapy target for HCC.

Indexed as

AnimalsAntigens, NeoplasmCarcinoma, HepatocellularCell Adhesion MoleculesCell Cycle ProteinsEpithelial Cell Adhesion MoleculeGene Expression ProfilingGene Expression Regulation, NeoplasticHumansLiver NeoplasmsMultigene FamilyNeoplastic Stem CellsPolo-Like Kinase 1Polycomb-Group ProteinsProtein Serine-Threonine KinasesProto-Oncogene ProteinsAntigens, NeoplasmCell Adhesion MoleculesCell Cycle ProteinsEpithelial Cell Adhesion MoleculePolo-Like Kinase 1Polycomb-Group ProteinsProtein Serine-Threonine KinasesProto-Oncogene ProteinsRepressor Proteins

Identifiers

PMID20851183
PMCPMC3030925
OpenAlexW1994537160

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.