Evidence map›Paper›PMID 18922900›Full record

ArticleCancer research2008

Suppression of the negative regulator LRIG1 contributes to ErbB2 overexpression in breast cancer.

Jamie K Miller, David L Shattuck, Ellen Q Ingalla, Lily Yen, Alexander D Borowsky, Lawrence J T Young, Robert D Cardiff, Kermit L Carraway, Colleen Sweeney

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

70 citing papers in PubMed, 1 synthesis or guideline pooled it, 120 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  11. The European respiratory journal · 2022
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  17. Review
  18. Development of thermosensitive resiquimod-loaded liposomes for enhanced cancer immunotherapy.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Article
  19. Low-frequency ultrasound-mediated cytokine transfection enhances T cell recruitment at local and distant tumor sites.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  20. Article

10 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

9 authors at 1 institution in 1 country.

Jamie K MillerSchool of Medicine, Davis Cancer Center, University of California at Davis, Sacramento, California 95817, USA.
David L Shattuck
Ellen Q Ingalla
Lily Yen
Alexander D Borowsky
Lawrence J T Young
Robert D Cardiff
Kermit L Carraway
Colleen Sweeney
University of California, Davis · US

Funding

Mechanisms of Receptor Tyrosine Kinase InhibitionR01CA118384 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI SWEENEY, COLLEEN ANN · 2006 to 2016
$2.4M
Modulation of ErbB Receptor Tyrosine Kinase SignalingR01GM068994 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI CARRAWAY, KERMIT L · 2003 to 2011
$2.4M
NCI NIH HHS CA118384NCI NIH HHS R01 CA118384NIGMS NIH HHS GM068994NIGMS NIH HHS R01 GM068994
6 · The paper itself

Abstract

The ErbB2 receptor tyrosine kinase is overexpressed in approximately 25% of breast tumors and contributes to poor patient prognosis and therapeutic resistance. Here, we examine the role of the recently discovered ErbB negative regulator LRIG1 in ErbB2(+) breast cancer. We observe that LRIG1 protein levels are significantly suppressed in ErbB2-induced mammary tumors in transgenic mice as well as in the majority of ErbB2(+) human breast tumors. These observations raise the possibility that LRIG1 loss could contribute to the initiation or growth of ErbB2(+) breast tumors. RNA interference-mediated knockdown of endogenous LRIG1 in the ErbB2-overexpressing breast tumor cell lines MDA-MB-453 and BT474 further elevates ErbB2 in these cells and augments cellular proliferation. In contrast, ectopic expression of LRIG1 reverses these trends. Interestingly, we observe that LRIG1 protein levels are suppressed in response to ErbB receptor activation in breast tumor cells but are unaffected by ErbB activation in immortalized nontransformed breast epithelial cells. Our observations indicate that the suppression of LRIG1 protein levels is a common feature of breast tumors. Moreover, our observations point to the existence of a feed-forward regulatory loop in breast tumor cells where aberrant ErbB2 signaling suppresses LRIG1 protein levels, which in turn contributes to ErbB2 overexpression.

Indexed as

AnimalsBreast NeoplasmsCell Line, TumorErb-b2 Receptor Tyrosine KinasesFemaleGenes, erbB-2HumansMembrane GlycoproteinsMiceMice, TransgenicNerve Tissue ProteinsSignal TransductionERBB2 protein, humanErbb2 protein, mouseErb-b2 Receptor Tyrosine KinasesLRIG1 protein, humanLrig1 protein, mouseMembrane GlycoproteinsNerve Tissue Proteins

Identifiers

PMID18922900
PMCPMC2597648
OpenAlexW2155626507

What OpenQuestion holds

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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.