Evidence map›Paper›PMID 23591595›Full record

ArticleClinical & experimental metastasis2013

Signaling for lymphangiogenesis via VEGFR-3 is required for the early events of metastasis.

Masataka Matsumoto, Sally Roufail, Rachael Inder, Carol Caesar, Tara Karnezis, Ramin Shayan, Rae H Farnsworth, Teruhiko Sato, Marc G Achen, G Bruce Mann and 1 more

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In one paragraph

Article in Clinical & experimental metastasis, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

21 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
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  11. Feline Mammary Cancer.Veterinary pathology · 2017
    Article
  12. Article
  13. [Advance in Research of Angiotensin II and Its Receptor and Malignant Tumor].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2016
    Review
  14. Article
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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

11 authors at 4 institutions in 2 countries.

Masataka MatsumotoLudwig Institute for Cancer Research, Royal Melbourne Hospital, P.O. Box 2008, Parkville, VIC, 3050, Australia.
Sally Roufail
Rachael Inder
Carol Caesar
Tara Karnezis
Ramin Shayan
Rae H Farnsworth
Teruhiko Sato
Marc G Achen
G Bruce Mann
Steven A Stacker
The Royal Melbourne Hospital · AULudwig Cancer Research · AUUniversity of Melbourne · AUPeter MacCallum Cancer Centre · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastasis to regional lymph nodes is an important and early event in many tumors. Vascular endothelial growth factor-C (VEGF-C), VEGF-D and their receptor VEGFR-3, play a role in tumor spread via the lymphatics, although the timing of their involvement is not understood. In contrast, VEGFR-2, activated by VEGF-A, VEGF-C and VEGF-D, is a mediator of angiogenesis and drives primary tumor growth. We demonstrate the critical role for VEGFR-3, but not VEGFR-2, in the early events of metastasis. In a tumor model exhibiting both VEGF-D-dependent angiogenesis and lymphangiogenesis, an antibody to VEGFR-2 (DC101) was capable of inhibiting angiogenesis (79 % reduction in PECAM + blood vessels) and growth (93 % reduction in tumor volume). However, unlike an anti-VEGFR-3 Mab (mF4-31C1), DC101 was not capable of eliminating either tumor lymphangiogenesis or lymphogenous metastasis (60 % reduction of lymph node metastasis by DC101 vs 95 % by mF4-31C1). Early excision of the primary tumors demonstrated that VEGF-D-mediated tumor spread precedes angiogenesis-induced growth. Small but highly metastatic primary human breast cancers had significantly higher lymphatic vessel density (23.1 vessels/mm(2)) than size-matched (11.7) or larger non-metastatic tumors (12.4) thus supporting the importance of lymphatic vessels, as opposed to angiogenesis-mediated primary tumor growth, for nodal metastasis. These results suggest that lymphangiogenesis via VEGF-D is more critical than angiogenesis for nodal metastasis.

Indexed as

AnimalsCell Line, TumorFemaleHumansLymphangiogenesisLymphatic MetastasisLymphatic VesselsMiceMice, SCIDNeovascularization, PhysiologicSignal TransductionVascular Endothelial Growth Factor DVascular Endothelial Growth Factor Receptor-2Vascular Endothelial Growth Factor Receptor-3FLT4 protein, humanVascular Endothelial Growth Factor DVascular Endothelial Growth Factor Receptor-2Vascular Endothelial Growth Factor Receptor-3

Identifiers

PMID23591595
OpenAlexW2065850348

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.