Evidence map›Paper›PMID 21741599›Full record

ArticleCancer cell2011

Proinvasion metastasis drivers in early-stage melanoma are oncogenes.

Kenneth L Scott, Cristina Nogueira, Timothy P Heffernan, Remco van Doorn, Sabin Dhakal, Jason A Hanna, Chengyin Min, Mariela Jaskelioff, Yonghong Xiao, Chang-Jiun Wu and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

87 citing papers in PubMed, 138 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. FTO promotes multiple myeloma progression by posttranscriptional activation of HSF1 in an mMolecular therapy : the journal of the American Society of Gene Therapy · 2022
    Article
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  14. Article
  15. Article
  16. Article
  17. Rapamycin Promotes ROS-Mediated Cell DeathFrontiers in oncology · 2021
    Article
  18. Prognostic Significance of ACP5 in Human Gastric Cancer.Digestive diseases (Basel, Switzerland) · 2021
    Article
  19. Article
  20. Kockdown of ACP5 inhibits hepatocellular carcinoma progression.American journal of translational research · 2020
    Article

27 more citing papers are in PubMed but not listed here.

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

22 authors at 7 institutions in 3 countries.

Kenneth L ScottBelfer Institute for Applied Cancer Science, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Cristina Nogueira
Timothy P Heffernan
Remco van Doorn
Sabin Dhakal
Jason A Hanna
Chengyin Min
Mariela Jaskelioff
Yonghong Xiao
Chang-Jiun Wu
Lisa A Cameron
Samuel R Perry
Rhamy Zeid
Tamar Feinberg
Minjung Kim
George Vande Woude
Scott R Granter
Marcus Bosenberg
Gerald C Chu
Ronald A DePinho
David L Rimm
Lynda Chin
Dana-Farber Cancer Institute · USYale University · USBrigham and Women's Hospital · USHarvard University · USLeiden University Medical Center · NLUniversidade do Porto · PTVan Andel Institute · US

Funding

Targeting Raf in Melanoma: Mechanisms for Effect & Resistance & Opportunities forP50CA093683 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI GOLUB, TODD R. · 2001 to 2012
$25.8M
MOUSE MODEL OF MALIGNANT MELANOMAU01CA084313 · NCI · DANA-FARBER CANCER INSTITUTE · PI DEPINHO, RONALD ANTHONY · 1999 to 2008
$7.4M
The genetic Basis of Melanoma MetastasisR01CA093947 · NCI · DANA-FARBER CANCER INSTITUTE · PI CHIN, LYNDA · 2002 to 2011
$3.6M
NCI NIH HHS P50 CA093683NCI NIH HHS P50 CA93683NCI NIH HHS R01 CA093947NCI NIH HHS R01 CA93947NCI NIH HHS U01 CA084313NCI NIH HHS U01 CA84313
6 · The paper itself

Abstract

Clinical and genomic evidence suggests that the metastatic potential of a primary tumor may be dictated by prometastatic events that have additional oncogenic capability. To test this "deterministic" hypothesis, we adopted a comparative oncogenomics-guided function-based strategy involving: (1) comparison of global transcriptomes of two genetically engineered mouse models with contrasting metastatic potential, (2) genomic and transcriptomic profiles of human melanoma, (3) functional genetic screen for enhancers of cell invasion, and (4) evidence of expression selection in human melanoma tissues. This integrated effort identified six genes that are potently proinvasive and oncogenic. Furthermore, we show that one such gene, ACP5, confers spontaneous metastasis in vivo, engages a key pathway governing metastasis, and is prognostic in human primary melanomas.

Indexed as

Acid PhosphataseAnimalsCell LineageConserved SequenceEvolution, MolecularGene Expression ProfilingGene Expression Regulation, NeoplasticGenomeHumansIsoenzymesKaplan-Meier EstimateMelanomaMiceNeoplasm InvasivenessNeoplasm MetastasisNeoplasm StagingAcid PhosphataseACP5 protein, humanAcp5 protein, mouseIsoenzymesTartrate-Resistant Acid Phosphatase

Identifiers

PMID21741599
PMCPMC3176328
OpenAlexW2034550661

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.