Evidence map›Paper›PMID 15901826›Full record

ArticleMolecular & cellular proteomics : MCP2005

Metabolic activation-related CD147-CD98 complex.

Daosong Xu, Martin E Hemler

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

81 citing papers in PubMed, 160 citations in OpenAlex.

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  18. Heteromeric Solute Carriers: Function, Structure, Pathology and Pharmacology.Advances in experimental medicine and biology · 2021
    Review
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  20. Article

21 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

2 authors at 2 institutions in 1 country.

Daosong XuDana-Farber Cancer Institute and Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Martin E Hemler
Dana-Farber Cancer Institute · USHarvard University · US

Funding

Interactions of CD147 Involved in MMP InductionR01CA102034 · NCI · DANA-FARBER CANCER INSTITUTE · PI HEMLER, MARTIN E · 2004 to 2008
$1.4M
NCI NIH HHS CA102034NCI NIH HHS R01 CA102034
6 · The paper itself

Abstract

Cell surface CD147 protein promotes production of matrix metalloproteinases and hyaluronan, associates with monocarboxylate transporters and integrins, and is involved in reproductive, neural, inflammatory, and tumor functions. Here we combined covalent cross-linking, mass spectrometric protein identification, and co-immunoprecipitation to show selective CD147 association with three major types of transporters (CD98 heavy chain (CD98hc)-L-type amino acid transporter, ASCT2, and monocarboxylate transporters) as well as a regulator of cell proliferation (epithelial cell adhesion molecule). In the assembly of these multicomponent complexes, CD147 and CD98hc play a central organizing role. RNA interference knock-down experiments established a strong connection between CD147 and CD98hc expression and a strong positive association of CD147 (and CD98hc) with cell proliferation. As the CD147-CD98hc complex and proliferation diminished, AMP-activated protein kinase (a cellular "fuel gauge") became activated, indicating a disturbance of cellular energy metabolism. Our data point to a CD147-CD98 cell surface supercomplex that plays a critical role in energy metabolism, likely by coordinating transport of lactate and amino acids. Furthermore we showed how covalent cross-linking, together with mass spectrometry, can be used to identify closely associated transmembrane proteins. This approach should also be applicable to many other types of transmembrane proteins besides those associated with CD98hc and CD147.

Indexed as

AMP-Activated Protein KinasesAntigens, CDBasiginBlotting, WesternBreast NeoplasmsCell MembraneCell ProliferationCells, CulturedChromatography, LiquidCross-Linking ReagentsFusion Regulatory Protein 1, Heavy ChainHumansImmunoprecipitationKidneyMembrane ProteinsMultienzyme ComplexesAMP-Activated Protein KinasesAntigens, CDBasiginBSG protein, humanCross-Linking ReagentsFusion Regulatory Protein 1, Heavy ChainMembrane ProteinsMultienzyme ComplexesProtein Serine-Threonine Kinases

Identifiers

PMID15901826
PMCPMC1351277
OpenAlexW2139405623

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.