Evidence map›Paper›PMID 35602406›Full record

ArticleNature cardiovascular research2022

Apelin-driven endothelial cell migration sustains intestinal progenitor cells and tumor growth.

Jeremiah Bernier-Latmani, Christophe Cisarovsky, Samantha Mahfoud, Simone Ragusa, Isabelle Dupanloup, David Barras, François Renevey, Sina Nassiri, Pascale Anderle, Mario Leonardo Squadrito and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in Nature cardiovascular research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

13 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Apelin/APJ: Another Player in the Cancer Biology Network.International journal of molecular sciences · 2025
    Review
  5. Review
  6. Transport functions of intestinal lymphatic vessels.Nature reviews. Gastroenterology & hepatology · 2025
    Review
  7. Review
  8. Article
  9. Review
  10. Mechanisms and functions of intestinal vascular specialization.The Journal of experimental medicine · 2024
    Review
  11. Article
  12. Review
  13. ADAMTS18Nature communications · 2022
    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

22 authors at 7 institutions in 4 countries.

Jeremiah Bernier-LatmaniDepartment of Oncology, Ludwig Center for Cancer Research Lausanne and University of Lausanne, Lausanne, Switzerland.
Christophe CisarovskyDepartment of Oncology, Ludwig Center for Cancer Research Lausanne and University of Lausanne, Lausanne, Switzerland.
Samantha MahfoudDepartment of Oncology, Ludwig Center for Cancer Research Lausanne and University of Lausanne, Lausanne, Switzerland.
Simone RagusaDepartment of Oncology, Ludwig Center for Cancer Research Lausanne and University of Lausanne, Lausanne, Switzerland.
Isabelle DupanloupBioinformatics Core Facility, SIB Swiss Institute of Bioinformatics, Lausanne, Switzerland.
David BarrasDepartment of Oncology, Ludwig Center for Cancer Research Lausanne and University of Lausanne, Lausanne, Switzerland.
François ReneveyDepartment of Biochemistry, University of Lausanne, Lausanne, Switzerland.
Sina NassiriSwiss Institute for Experimental Cancer Research (ISREC), School of Life Sciences, EPFL, Lausanne, Switzerland.
Pascale AnderleBioinformatics Core Facility, SIB Swiss Institute of Bioinformatics, Lausanne, Switzerland.
Mario Leonardo SquadritoSwiss Institute for Experimental Cancer Research (ISREC), School of Life Sciences, EPFL, Lausanne, Switzerland.
Stefanie SiegertDepartment of Biochemistry, University of Lausanne, Lausanne, Switzerland.
Suzel DavantureDepartment of Oncology, Ludwig Center for Cancer Research Lausanne and University of Lausanne, Lausanne, Switzerland.
Alejandra González-LoyolaDepartment of Oncology, Ludwig Center for Cancer Research Lausanne and University of Lausanne, Lausanne, Switzerland.
Nadine FournierBioinformatics Core Facility, SIB Swiss Institute of Bioinformatics, Lausanne, Switzerland.
Sanjiv A LutherDepartment of Biochemistry, University of Lausanne, Lausanne, Switzerland.
Rui BeneditoCentro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain.
Philippe ValetInstitut RESTORE, UMR 1301-INSERM, 5070-CNRS, Université Paul Sabatier, Université de Toulouse, Toulouse, France.
Bin ZhouState Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, Shanghai, China.
Michele De PalmaSwiss Institute for Experimental Cancer Research (ISREC), School of Life Sciences, EPFL, Lausanne, Switzerland.
Mauro DelorenziDepartment of Oncology, Ludwig Center for Cancer Research Lausanne and University of Lausanne, Lausanne, Switzerland.
Christine SempouxInstitute of Pathology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Tatiana V PetrovaDepartment of Oncology, Ludwig Center for Cancer Research Lausanne and University of Lausanne, Lausanne, Switzerland.
Ludwig Cancer Research · CHSIB Swiss Institute of Bioinformatics · CHUniversity of Lausanne · CHÉcole Polytechnique Fédérale de Lausanne · CHCentre National de la Recherche Scientifique · FRChinese Academy of Sciences · CNSpanish National Centre for Cardiovascular Research · ES

Funding

European Research Council 725051Swiss National Science Foundation 156266Swiss National Science Foundation 166161
6 · The paper itself

Abstract

Stem and progenitor cells residing in the intestinal crypts drive the majority of colorectal cancers (CRCs), yet vascular contribution to this niche remains largely unexplored. VEGFA is a key driver of physiological and tumor angiogenesis. Accordingly, current anti-angiogenic cancer therapies target the VEGFA pathway. Here we report that in CRC expansion of the stem/progenitor pool in intestinal crypts requires VEGFA-independent growth and remodeling of blood vessels. Epithelial transformation induced expression of the endothelial peptide apelin, directs migration of distant venous endothelial cells towards progenitor niche vessels ensuring optimal perfusion. In the absence of apelin, loss of injury-inducible PROX1+ epithelial progenitors inhibited both incipient and advanced intestinal tumor growth. Our results establish fundamental principles for the reciprocal communication between vasculature and the intestinal progenitor niche and provide a mechanism for resistance to VEGFA-targeting drugs in CRCs.

Identifiers

PMID35602406
PMCPMC7612746
OpenAlexW4280602829

What OpenQuestion holds

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Registered trials

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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.