Evidence map›Paper›PMID 12789268›Full record

ArticleOncogene2003

Atypical expression of ErbB3 in myeloma cells: cross-talk between ErbB3 and the interferon-alpha signaling complex.

Denise K Walters, Jena D French, Bonnie K Arendt, Diane F Jelinek

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Targeting ErbB3: the New RTK(id) on the Prostate Cancer Block.Immunology, endocrine & metabolic agents in medicinal chemistry · 2011
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Mechanisms of resistance to Erbitux (anti-epidermal growth factor receptor) combination therapy in pancreatic adenocarcinoma cells.Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract · 2004
    Article
  11. Article
  12. Article
  13. Review
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.

Denise K WaltersDepartment of Immunology, Tumor Biology Program, Mayo Graduate and Medical Schools, Mayo Clinic/Foundation, Rochester, MN 55905, USA.
Jena D French
Bonnie K Arendt
Diane F Jelinek
Mayo Clinic · US

Funding

TISSUE BANK AND CLINICAL/LABORATORY DATABASEP01CA062242 · NCI · MAYO CLINIC ROCHESTER · PI THERNEAU, TERRY M · 1994 to 2009
$12.9M
MOLECULAR AND BIOLOGICAL FUNCTION OF CD40 IN MYELOMAR01CA062228 · NCI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI JELINEK, DIANE F · 1995 to 2002
$629k
MOLECULAR AND BIOLOGICAL FUNCTIONS OF CD40 IN MYELOMAR55CA062228 · NCI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI JELINEK, DIANE F · 1994 to 1994
–
NCI NIH HHS CA62228NCI NIH HHS CA62242
6 · The paper itself

Abstract

We have previously demonstrated that the responsiveness of multiple myeloma (MM) cells to interferon-alpha (IFN-alpha) stimulation is variable, with an atypical growth response displayed by some cells. Here we report the ability of IFN-alpha to induce tyrosine phosphorylation of a 180 kDa band in the KAS-6/1 MM cell line, which is growth responsive to IFN-alpha. Further characterization demonstrated that this band corresponds to ErbB3. To our knowledge, this is the first report of ErbB3 expression in a cell type of the hematopoietic lineage. Although ErbB receptors have been shown to crosscommunicate with various other receptors, our results show for the first time that the IFN-alpha receptor can crosscommunicate with ErbB3. To address the significance of these observations, we transfected ErbB3-negative DP-6 MM cells with ErbB3 and used siRNA to silence ErbB3 in the KAS-6/1 cell line. Although IFN-alpha transactivated ErbB3 in the DP-6 transfectants, it did not confer growth responsiveness to IFN-alpha. Interestingly, silencing ErbB3 expression in the KAS-6/1 cells decreased the overall growth response to IFN-alpha and to interleukin-6. These results suggest that ErbB3 expression alone does not uniquely confer IFN-alpha growth responsiveness, but instead may amplify proliferation rates in MM cells that have acquired atypical expression of this receptor.

Indexed as

Cell DivisionDNA-Binding ProteinsDown-RegulationEnzyme ActivationFemaleGene Expression Regulation, NeoplasticHumansInterferon-alphaKineticsMacromolecular SubstancesMitogen-Activated Protein KinasesMultiple MyelomaPhosphorylationReceptor Cross-TalkReceptor, ErbB-3Receptor, Interferon alpha-betaDNA-Binding ProteinsInterferon-alphaMacromolecular SubstancesMitogen-Activated Protein KinasesReceptor, ErbB-3Receptor, Interferon alpha-betaReceptors, InterferonRNA, Small InterferingSTAT3 protein, humanSTAT3 Transcription FactorTrans-ActivatorsTyrosine

Identifiers

PMID12789268
OpenAlexW2142708037

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.