Evidence map›Paper›PMID 26777415›Full record

ArticleCancer cell2015

Constitutive Activation of mTORC1 in Endothelial Cells Leads to the Development and Progression of Lymphangiosarcoma through VEGF Autocrine Signaling.

Shaogang Sun, Song Chen, Fei Liu, Haige Wu, Jonathan McHugh, Ingrid L Bergin, Anita Gupta, Denise Adams, Jun-Lin Guan

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2015. 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
2.9field-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, 64 citations in OpenAlex.

  1. Article
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  14. Autocrine/Paracrine Slit-Robo Signaling Controls Optic Lobe Development inFrontiers in cell and developmental biology · 2022
    Article
  15. Article
  16. Article
  17. Role of TSC1 in physiology and diseases.Molecular and cellular biochemistry · 2021
    Review
  18. Article
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  20. 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

9 authors at 4 institutions in 1 country.

Shaogang SunDepartment of Cancer Biology, College of Medicine, University of Cincinnati, Cincinnati, OH 45267, USA.
Song ChenDepartment of Cancer Biology, College of Medicine, University of Cincinnati, Cincinnati, OH 45267, USA.
Fei LiuDepartment of Biologic and Materials Sciences, University of Michigan, Ann Arbor, MI 48109, USA.
Haige WuDepartment of Cancer Biology, College of Medicine, University of Cincinnati, Cincinnati, OH 45267, USA.
Jonathan McHughDepartment of Pathology, University of Michigan, Ann Arbor, MI 48109, USA.
Ingrid L BerginUnit for Laboratory Animal Medicine, University of Michigan, Ann Arbor, MI 48109, USA.
Anita GuptaDepartment of Pathology, Cincinnati Children's Hospital Medical Center, College of Medicine, University of Cincinnati, Cincinnati, OH 45267, USA.
Denise AdamsDepartment of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, OH 45267, USA.
Jun-Lin GuanDepartment of Cancer Biology, College of Medicine, University of Cincinnati, Cincinnati, OH 45267, USA. Electronic address: guanjl@uc.edu.
University of Cincinnati · USUniversity of Michigan–Ann Arbor · USCincinnati Children's Hospital Medical Center · USUniversity of Cincinnati Medical Center · US

Funding

Mechanisms of progression of vascular malformation to lymphangiosarcomaR01HL073394 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GUAN, JUN-LIN · 2003 to 2025
$8.4M
The Mechanisms of Bone Mass Regulation by FIP200R01AR062030 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIU, FEI · 2012 to 2016
$1.7M
Genetic Analysis of FAK kinase and scaffold functions in breast cancerR01CA163493 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GUAN, JUN-LIN · 2012 to 2016
$1.6M
Molecular Analysis of Signal Transduction in Cancer Development and ProgressionR01CA150926 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GUAN, JUN-LIN · 2010 to 2014
$1.4M
The Mechanism of Excess Neural Crest-Derived Craniofacial Bone Formation in a MouR03DE021718 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIU, FEI · 2011 to 2012
$233k
NCI NIH HHS CA150926NCI NIH HHS CA163493NCI NIH HHS R01 CA150926NCI NIH HHS R01 CA163493NHLBI NIH HHS HL073394NHLBI NIH HHS R01 HL073394NIAMS NIH HHS AR062030NIAMS NIH HHS R01 AR062030NIDCR NIH HHS DE021718NIDCR NIH HHS R03 DE021718
6 · The paper itself

Abstract

Angiosarcoma/lymphangiosarcoma is a rare malignancy with poor prognosis. We generated a mouse model with inducible endothelial-cell-specific deletion of Tsc1 to examine mTORC1 signaling in lymphangiosarcoma. Tsc1 loss increased retinal angiogenesis in neonates and led to endothelial proliferative lesions from vascular malformations to vascular tumors in adult mice. Sustained mTORC1 signaling was required for lymphangiosarcoma development and maintenance. Increased VEGF expression in tumor cells was seen, and blocking autocrine VEGF signaling abolished vascular tumor development and growth. We also found significant correlations between mTORC1 activation and VEGF, HIF1α, and c-Myc expression in human angiosarcoma samples. These studies demonstrated critical mechanisms of aberrant mTORC1 activation in lymphangiosarcoma and validate the mice as a valuable model for further study.

Indexed as

Autocrine CommunicationNeovascularization, PathologicAngiogenesis InhibitorsAnimalsCell MovementCell ProliferationCells, CulturedCell Transformation, NeoplasticEndothelial CellsEnzyme ActivationGenotypeHumansHypoxia-Inducible Factor 1, alpha SubunitLymphangiosarcomaMechanistic Target of Rapamycin Complex 1Mice, KnockoutAngiogenesis InhibitorsHIF1A protein, humanHif1a protein, mouseHypoxia-Inducible Factor 1, alpha SubunitMechanistic Target of Rapamycin Complex 1Multiprotein ComplexesMYC protein, humanMyc protein, mouseProtein Kinase InhibitorsProto-Oncogene Proteins c-mycReceptors, Vascular Endothelial Growth FactorTOR Serine-Threonine KinasesTSC1 protein, humanTsc1 protein, mouseTuberous Sclerosis Complex 1 ProteinTumor Suppressor ProteinsVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouseVEGFA protein, human

Identifiers

PMID26777415
PMCPMC4828306
OpenAlexW2222242135

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.