Evidence map›Paper›PMID 28657426›Full record

ReviewSmall GTPases2019

Oncogenic Ect2 signaling regulates rRNA synthesis in NSCLC.

Verline Justilien, Kayla C Lewis, Nicole R Murray, Alan P Fields

Open access · bronzeAbstract readReviewVideo-Audio Media
In one paragraph

Review in Small GTPases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

20 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. The homeostatic regulation of ribosome biogenesis.Seminars in cell & developmental biology · 2023
    Review
  6. Article
  7. Cancers · 2022
    Article
  8. Cancers · 2022
    Article
  9. Article
  10. Article
  11. Protein kinase CCell reports · 2021
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  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

4 authors at 1 institution in 1 country.

Verline Justiliena Department of Cancer Biology, Mayo Clinic Comprehensive Cancer Center , Jacksonville , FL , USA.
Kayla C Lewisa Department of Cancer Biology, Mayo Clinic Comprehensive Cancer Center , Jacksonville , FL , USA.
Nicole R Murraya Department of Cancer Biology, Mayo Clinic Comprehensive Cancer Center , Jacksonville , FL , USA.
Alan P Fieldsa Department of Cancer Biology, Mayo Clinic Comprehensive Cancer Center , Jacksonville , FL , USA.
Mayo Clinic in Florida · US

Funding

Three-Dimensional Organoid Cultures to Investigate 3q26 Driver Functions in Multiple Lung Cancer Cells of OriginR01CA081436 · NCI · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI FIELDS, ALAN P. · 1999 to 2022
$9.9M
Atypical PKC signaling in lung cancer stem cellsR21CA151250 · NCI · MAYO CLINIC JACKSONVILLE · PI FIELDS, ALAN P. · 2010 to 2011
$529k
Ect2 Function in Lung Adenocarcinoma Initiation and MaintenanceR21CA204938 · NCI · MAYO CLINIC JACKSONVILLE · PI JUSTILIEN, VERLINE · 2016 to 2017
$402k
The pathophysiology and palliation of the paclitaxel-induced acute pain syndromeR21CA180997 · NCI · MAYO CLINIC ROCHESTER · PI FIELDS, ALAN P., JATOI, AMINAH · 2014 to 2015
$365k
NCI NIH HHS R01 CA081436NCI NIH HHS R21 CA151250NCI NIH HHS R21 CA180997NCI NIH HHS R21 CA204938
6 · The paper itself

Abstract

The Rho GTPase family members Rac1, Cdc42 and RhoA play key contributory roles in the transformed phenotype of human cancers. Epithelial Cell Transforming Sequence 2 (Ect2), a guanine nucleotide exchange factor (GEF) for these Rho GTPases, has also been implicated in a variety of human cancers. We have shown that Ect2 is frequently overexpressed in both major forms of non-small cell lung cancer (NSCLC), lung adenocarcinoma (LADC) and lung squamous cell carcinoma (LSCC), which together make up approximately 70% of all lung cancer diagnoses. Furthermore, we have found that Ect2 is required for multiple aspects of the transformed phenotype of NSCLC cells including transformed growth and invasion

Indexed as

Signal TransductionAnimalsCarcinogenesisCarcinoma, Non-Small-Cell LungHumansLung NeoplasmsNeoplasm InvasivenessProto-Oncogene ProteinsRibosomesRNA, NeoplasmRNA, RibosomalECT2 protein, humanProto-Oncogene ProteinsRNA, NeoplasmRNA, RibosomalEct2non-small cell lung cancerribosome biogenesisrRNA synthesis

Identifiers

PMID28657426
PMCPMC6748369
OpenAlexW2729569868

What OpenQuestion holds

Textmetadata
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.