Evidence map›Paper›PMID 25506915›Full record

ArticlePloS one2014

A subpopulation of circulating endothelial cells express CD109 and is enriched in the blood of cancer patients.

Patrizia Mancuso, Angelica Calleri, Giuliana Gregato, Valentina Labanca, Jessica Quarna, Pierluigi Antoniotti, Lucia Cuppini, Gaetano Finocchiaro, Marica Eoli, Vittorio Rosti and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. 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
1.1field-weighted citation impact, top 22% 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, 19 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Expression and prognostic potential of TMEM204: a pan-cancer analysis.International journal of clinical and experimental pathology · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. A Review of Anti-Angiogenic Targets for Monoclonal Antibody Cancer Therapy.International journal of molecular sciences · 2017
    Review
  10. Novel role for p56/Lck in regulation of endothelial cell survival and angiogenesis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016
    Article
  11. Article
  12. Article
  13. 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

11 authors at 3 institutions in 1 country.

Patrizia MancusoLaboratory of Hematology-Oncology, European Institute of Oncology, Milan, Italy.
Angelica CalleriLaboratory of Hematology-Oncology, European Institute of Oncology, Milan, Italy.
Giuliana GregatoLaboratory of Hematology-Oncology, European Institute of Oncology, Milan, Italy.
Valentina LabancaLaboratory of Hematology-Oncology, European Institute of Oncology, Milan, Italy.
Jessica QuarnaLaboratory of Hematology-Oncology, European Institute of Oncology, Milan, Italy.
Pierluigi AntoniottiLaboratory of Hematology-Oncology, European Institute of Oncology, Milan, Italy.
Lucia CuppiniDepartment of Neuro-Oncology, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
Gaetano FinocchiaroDepartment of Neuro-Oncology, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
Marica EoliDepartment of Neuro-Oncology, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
Vittorio RostiCenter for the Study and Treatment of Myelofibrosis, Research Laboratories of Biotechnology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Francesco BertoliniLaboratory of Hematology-Oncology, European Institute of Oncology, Milan, Italy.
European Institute of Oncology · ITFondazione IRCCS Istituto Neurologico Carlo Besta · ITIstituti di Ricovero e Cura a Carattere Scientifico · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe endothelium is not a homogeneous organ. Endothelial cell heterogeneity has been described at the level of cell morphology, function, gene expression, and antigen composition. As a consequence of the genetic, transcriptome and surrounding environment diversity, endothelial cells from different vascular beds have differentiated functions and phenotype. Detection of circulating endothelial cells (CECs) by flow cytometry is an approach widely used in cancer patients, and their number, viability and kinetic is a promising tool to stratify patient receiving anti-angiogenic treatment. METHODOLOGY/PRINCIPAL

findingsCurrently CECs are identified as positive for a nuclear binding antigen (DNA+), negative for the pan leukocyte marker CD45, and positive for CD31 and CD146. Following an approach recently validated in our laboratory, we investigated the expression of CD109 on CECs from the peripheral blood of healthy subject and cancer patients. The endothelial nature of these cells was validated by RT-PCR for the presence of m-RNA level of CDH5 (Ve-Cadherin) and CLDN5 (Claudin5), two endothelial specific transcripts. Before treatment, significantly higher levels of CD109+ CECs and viable CD109+CECs were found in breast cancer patients and glioblastoma patients compared to healthy controls, and their number significantly decreased after treatment. Higher levels of endothelial specific transcripts expressed in developing endothelial cells CLEC14a, TMEM204, ARHGEF15, GPR116, were observed in sorted CD109+CECs when compared to sorted CD146+CECs, suggesting that these genes can play an important role not only during embryogenesis but also in adult angiogenesis. Interestingly, mRNA levels of TEM8 (identified as Antrax Toxin Receptor1, Antrax1) were expressed in CD109+CECs+ but not in CD146+CECs.

conclusionTaken together our results suggest that CD109 represent a rare population of circulating tumor endothelial cells, that play a potentially useful prognostic role in patients with glioblastoma. The role of CD109 expression in cancer vessel-specific endothelial cells deserves to be further investigated by gene expression studies.

Indexed as

AdultAgedAntigens, CDBreast NeoplasmsCD146 AntigenEndothelial CellsFemaleGene Expression Regulation, NeoplasticGlioblastomaGPI-Linked ProteinsHumansMaleMiddle AgedNeoplasm ProteinsNeoplasmsNeoplastic Cells, CirculatingAntigens, CDCD109 protein, humanCD146 AntigenGPI-Linked ProteinsNeoplasm Proteins

Identifiers

PMID25506915
PMCPMC4266608
OpenAlexW2153273886

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.