Evidence map›Paper›PMID 20805499›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2010

Endosomal-sorting complexes required for transport (ESCRT) pathway-dependent endosomal traffic regulates the localization of active Src at focal adhesions.

Chun Tu, Cesar F Ortega-Cava, Paul Winograd, Marissa Jo Stanton, Alagarsamy Lakku Reddi, Ingrid Dodge, Ranjana Arya, Manjari Dimri, Robert J Clubb, Mayumi Naramura and 3 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.5field-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

43 citing papers in PubMed, 72 citations in OpenAlex.

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  11. Historical retrospective of theMolecular and clinical oncology · 2020
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  12. Flotillin membrane domains in cancer.Cancer metastasis reviews · 2020
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  18. Review
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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

13 authors at 7 institutions in 2 countries.

Chun TuEppley Institute for Research in Cancer and Allied Diseases and University of Nebraska Medical Center-Eppley Cancer Center, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Cesar F Ortega-Cava
Paul Winograd
Marissa Jo Stanton
Alagarsamy Lakku Reddi
Ingrid Dodge
Ranjana Arya
Manjari Dimri
Robert J Clubb
Mayumi Naramura
Kay-Uwe Wagner
Vimla Band
Hamid Band
University of Nebraska Medical Center · USJawaharlal Nehru University · INNorthShore University HealthSystem · USNorthwestern University · USPediatrics and Genetics · USPfizer (United States) · USUniversity of Wisconsin–Madison · US

Funding

TYROSINE KINASE REGULATION VIA PROTEIN DEGRADATIONR01CA087986 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BAND, HAMID · 2000 to 2015
$4.2M
MOLECULAR CONTROL OF EGF RECEPTOR DOWN-REGULATIONR01CA099163 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BAND, HAMID · 2003 to 2012
$3.7M
Targeting Endocytic Recycling of EGF Receptor in Cancer R01CA105489 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BAND, HAMID · 2004 to 2014
$3.0M
Tumor Susceptibility Gene 101 Deficiency and NeoplasiaR01CA093797 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI WAGNER, KAY-UWE · 2002 to 2013
$2.8M
A novel regulator of p53 functionR01CA096844 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BAND, VIMLA · 2002 to 2011
$2.7M
ADA3: a novel target for HPV16 E6 oncoproteinR01CA094143 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BAND, VIMLA · 2002 to 2006
$1.7M
ErbB2 Downregulation Through HSP90 InhibitionR01CA116552 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BAND, HAMID · 2007 to 2011
$1.4M
PDGF Receptor Regulation by CBLR01CA099900 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BAND, HAMID · 2003 to 2007
$1.1M
THE ROLE OF A NOVEL GAP IN EPITHELIAL ONCOGENESISR01CA081076 · NCI · TUFTS MEDICAL CENTER · PI BAND, VIMLA · 1999 to 2003
$988k
NCI NIH HHS CA105489NCI NIH HHS CA116552NCI NIH HHS CA81076NCI NIH HHS CA87986NCI NIH HHS CA93797NCI NIH HHS CA94143NCI NIH HHS CA96844NCI NIH HHS CA99163NCI NIH HHS CA99900NCI NIH HHS R01 CA081076NCI NIH HHS R01 CA087986NCI NIH HHS R01 CA093797NCI NIH HHS R01 CA094143NCI NIH HHS R01 CA096844NCI NIH HHS R01 CA099163NCI NIH HHS R01 CA099900NCI NIH HHS R01 CA105489NCI NIH HHS R01 CA116552
6 · The paper itself

Abstract

Active Src localization at focal adhesions (FAs) is essential for cell migration. How this pool is linked mechanistically to the large pool of Src at late endosomes (LEs)/lysosomes (LY) is not well understood. Here, we used inducible Tsg101 gene deletion, TSG101 knockdown, and dominant-negative VPS4 expression to demonstrate that the localization of activated cellular Src and viral Src at FAs requires the endosomal-sorting complexes required for transport (ESCRT) pathway. Tsg101 deletion also led to impaired Src-dependent activation of STAT3 and focal adhesion kinase and reduced cell migration. Impairment of the ESCRT pathway or Rab7 function led to the accumulation of active Src at aberrant LE/LY compartments followed by its loss. Analyses using fluorescence recovery after photo-bleaching show that dynamic mobility of Src in endosomes is ESCRT pathway-dependent. These results reveal a critical role for an ESCRT pathway-dependent LE/LY trafficking step in Src function by promoting localization of active Src to FAs.

Indexed as

AnimalsCell AdhesionCell MovementCells, CulturedDNA-Binding ProteinsEndosomal Sorting Complexes Required for TransportEndosomesHumansLysosomesMiceProtein Transportsrc-Family KinasesTranscription FactorsTsg101 ProteinDNA-Binding ProteinsEndosomal Sorting Complexes Required for Transportsrc-Family KinasesTranscription FactorsTsg101 Protein

Identifiers

PMID20805499
PMCPMC2941294
OpenAlexW2046416187

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.