Evidence map›Paper›PMID 29492715›Full record

ReviewClinical and experimental medicine2018

Mast cells and angiogenesis in pancreatic ductal adenocarcinoma.

Vito Longo, Roberto Tamma, Oronzo Brunetti, Salvatore Pisconti, Antonella Argentiero, Nicola Silvestris, Domenico Ribatti

Abstract readReview
PubMed Publisher
In one paragraph

Review in Clinical and experimental medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
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  12. Translational lung cancer research · 2025
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  18. Heterogeneity of tumor-infiltrating myeloid cells in era of single-cell genomics.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2022
    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

7 authors at 1 institution in 1 country.

Vito LongoDepartment of Medical Oncology, Hospital of Taranto, Taranto, Italy.
Roberto TammaDepartment of Basic Medical Sciences, Neurosciences and Sensory Organs, University of Bari Medical School, Bari, Italy.
Oronzo BrunettiMedical Oncology Unit and Scientific Directorate, Cancer Institute "Giovanni Paolo II", Viale Orazio Flacco, 65, 70124, Bari, Italy.
Salvatore PiscontiDepartment of Medical Oncology, Hospital of Taranto, Taranto, Italy.
Antonella ArgentieroMedical Oncology Unit and Scientific Directorate, Cancer Institute "Giovanni Paolo II", Viale Orazio Flacco, 65, 70124, Bari, Italy.
Nicola SilvestrisMedical Oncology Unit and Scientific Directorate, Cancer Institute "Giovanni Paolo II", Viale Orazio Flacco, 65, 70124, Bari, Italy. n.silvestris@oncologico.bari.it.ORCID http://orcid.org/0000-0001-7814-7318
Domenico RibattiDepartment of Basic Medical Sciences, Neurosciences and Sensory Organs, University of Bari Medical School, Bari, Italy.
Istituto Tumori Bari · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mast cells are recognized as critical components of the tumor stromal microenvironment in several solid and hematological malignancies, promoting angiogenesis and tumor growth. A correlation between mast cells infiltration, angiogenesis and tumor progression has been reported for pancreatic ductal adenocarcinoma as well. Mast cells contribute to the aggressiveness of the pancreatic ductal carcinoma enhancing the expression of several pro-angiogenic factors such as vascular endothelial growth factor, fibroblast growth factor-2, platelet-derived growth factor and angiopoietin-1 as well as stimulating the pancreatic cancer cells proliferation by IL-13 and tryptase. The disruption of this pro-angiogenic and proliferative stimulation by inhibiting the mast cells migration and degranulation is under investigation as a potential therapeutic approach in pancreatic ductal adenocarcinoma patients. This review will summarize the literature concerning the mast cells infiltration in the pancreatic ductal adenocarcinoma analyzing its role in angiogenesis and tumor progression.

Indexed as

Gene Expression Regulation, NeoplasticAngiogenesis InhibitorsAngiopoietin-1Carcinoma, Pancreatic DuctalCell MovementDisease ProgressionFibroblast Growth Factor 2HumansInterleukin-13Mast CellsNeoplasm InvasivenessNeovascularization, PathologicPancreatic NeoplasmsPlatelet-Derived Growth FactorTryptasesTumor MicroenvironmentAngiogenesis InhibitorsAngiopoietin-1Fibroblast Growth Factor 2IL13 protein, humanInterleukin-13Platelet-Derived Growth FactorTryptasesVascular Endothelial Growth Factor AVEGFA protein, humanAngiogenesisMast cellsPancreatic ductal adenocarcinoma

Identifiers

PMID29492715
OpenAlexW2792716055

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.