Evidence map›Paper›PMID 29259016›Full record

ArticleCancer research2018

Oncogenic RAS-Induced Perinuclear Signaling Complexes Requiring KSR1 Regulate Signal Transmission to Downstream Targets.

Sandip K Basu, Sook Lee, Jacqueline Salotti, Srikanta Basu, Krisada Sakchaisri, Zhen Xiao, Vijay Walia, Christopher J Westlake, Deborah K Morrison, Peter F Johnson

Abstract read
In one paragraph

Article in Cancer research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. The Paradoxical Role of Cellular Senescence in Cancer.Frontiers in cell and developmental biology · 2021
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. 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

10 authors at 2 institutions in 1 country.

Sandip K BasuMouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland.
Sook LeeMouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland.
Jacqueline SalottiMouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland.
Srikanta BasuMouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland.
Krisada SakchaisriMouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland.
Zhen XiaoLaboratory of Proteomics and Analytical Technologies, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, Maryland.
Vijay WaliaLaboratory of Cell and Developmental Signaling, Center for Cancer Research, National Cancer Institute, Frederick, Maryland.
Christopher J WestlakeLaboratory of Cell and Developmental Signaling, Center for Cancer Research, National Cancer Institute, Frederick, Maryland.
Deborah K MorrisonLaboratory of Cell and Developmental Signaling, Center for Cancer Research, National Cancer Institute, Frederick, Maryland.
Peter F JohnsonMouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland. johnsope@mail.nih.gov.
Frederick National Laboratory for Cancer Research · USLeidos (United States) · US

Funding

Role of CEBP transcription factors in regulating cell growth and tumorigenesisZIABC010328 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI JOHNSON, PETER F · 2009 to 2021
$17.5M
Role of Protein Scaffolds in RTKRas-dependent Signal TransductionZIABC011107 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MORRISON, DEBORAH · 2009 to 2025
$7.3M
Role of CEBP transcription factors in regulating cell growth and tumorigenesisZ01BC010328 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI JOHNSON, PETER · 2000 to 2008
$3.0M
Intramural NIH HHS Z01 BC010328Intramural NIH HHS Z99 CA999999Intramural NIH HHS ZIA BC010328
6 · The paper itself

Abstract

The precise characteristics that distinguish normal and oncogenic RAS signaling remain obscure. Here, we show that oncogenic RAS and BRAF induce perinuclear relocalization of several RAS pathway proteins, including the kinases CK2 and p-ERK1/2 and the signaling scaffold KSR1. This spatial reorganization requires endocytosis, the kinase activities of MEK-ERK and CK2, and the presence of KSR1. CK2α colocalizes with KSR1 and Rab11, a marker of recycling endosomes, whereas p-ERK associates predominantly with a distinct KSR1-positive endosomal population. Notably, these perinuclear signaling complexes (PSC) are present in tumor cell lines, mouse lung tumors, and mouse embryonic fibroblasts undergoing RAS-induced senescence. PSCs are also transiently induced by growth factors (GF) in nontransformed cells with delayed kinetics (4-6 hours), establishing a novel late phase of GF signaling that appears to be constitutively activated in tumor cells. PSCs provide an essential platform for RAS-induced phosphorylation and activation of the prosenescence transcription factor C/EBPβ in primary MEFs undergoing senescence. Conversely, in tumor cells, C/EBPβ activation is suppressed by 3'UTR-mediated localization of

Indexed as

A549 CellsAnimalsCCAAT-Enhancer-Binding Protein-betaCell Line, TumorHEK293 CellsHeLa CellsHep G2 CellsHumansMAP Kinase Signaling SystemMiceNIH 3T3 CellsPhosphorylationProtein Kinasesras ProteinsSignal TransductionCCAAT-Enhancer-Binding Protein-betaKSR-1 protein kinaseProtein Kinasesras Proteins

Identifiers

PMID29259016
PMCPMC5815900
OpenAlexW2780887074

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.