Evidence map›Paper›PMID 32019260›Full record

ReviewInternational journal of molecular sciences2020

CD155: A Multi-Functional Molecule in Tumor Progression.

Rosa Molfetta, Beatrice Zitti, Mario Lecce, Nadia Domenica Milito, Helena Stabile, Cinzia Fionda, Marco Cippitelli, Angela Gismondi, Angela Santoni, Rossella Paolini

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 3% 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

77 citing papers in PubMed, 1 synthesis or guideline pooled it, 111 citations in OpenAlex.

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17 more citing papers are in PubMed but not listed here.

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

10 authors at 1 institution in 1 country.

Rosa MolfettaDepartment of Molecular Medicine, "Sapienza" University of Rome, Laboratory affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, "Viale Regina Elena 291, 00161 Rome, Italy.
Beatrice ZittiDepartment of Molecular Medicine, "Sapienza" University of Rome, Laboratory affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, "Viale Regina Elena 291, 00161 Rome, Italy.
Mario LecceDepartment of Molecular Medicine, "Sapienza" University of Rome, Laboratory affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, "Viale Regina Elena 291, 00161 Rome, Italy.
Nadia Domenica MilitoDepartment of Molecular Medicine, "Sapienza" University of Rome, Laboratory affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, "Viale Regina Elena 291, 00161 Rome, Italy.
Helena StabileDepartment of Molecular Medicine, "Sapienza" University of Rome, Laboratory affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, "Viale Regina Elena 291, 00161 Rome, Italy.
Cinzia FiondaDepartment of Molecular Medicine, "Sapienza" University of Rome, Laboratory affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, "Viale Regina Elena 291, 00161 Rome, Italy.
Marco CippitelliDepartment of Molecular Medicine, "Sapienza" University of Rome, Laboratory affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, "Viale Regina Elena 291, 00161 Rome, Italy.
Angela GismondiDepartment of Molecular Medicine, "Sapienza" University of Rome, Laboratory affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, "Viale Regina Elena 291, 00161 Rome, Italy.
Angela SantoniDepartment of Molecular Medicine, "Sapienza" University of Rome, Laboratory affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, "Viale Regina Elena 291, 00161 Rome, Italy.
Rossella PaoliniDepartment of Molecular Medicine, "Sapienza" University of Rome, Laboratory affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, "Viale Regina Elena 291, 00161 Rome, Italy.
Istituto Pasteur · IT

Funding

Ministero dell'Istruzione, dell'Università e della Ricerca PRIN/20103FMJEN/AngelaSantoni
6 · The paper itself

Abstract

CD155 is an adhesion molecule belonging to the Nectin/Nectin-like family often overexpressed on tumor cells and involved in many different processes such as cell adhesion, migration and proliferation. In contrast to these pro-tumorigenic functions, CD155 is also a ligand for the activating receptor DNAM-1 expressed on cytotoxic lymphocytes including Natural Killer (NK) cells and involved in anti-tumor immune response. However, during tumor progression inhibitory receptors for CD155 are up-regulated on the surface of effector cells, contributing to an impairment of their cytotoxic capacity. In this review we will focus on the roles of CD155 as a ligand for the activating receptor DNAM-1 regulating immune surveillance against cancer and as pro-oncogenic molecule favoring tumor proliferation, invasion and immune evasion. A deeper understanding of the multiple roles played by CD155 in cancer development contributes to improving anti-tumor strategies aimed to potentiate immune response against cancer.

Indexed as

Disease ProgressionHumansImmunologic SurveillanceNeoplasmsReceptors, Viruspoliovirus receptorReceptors, VirusNatural Killer (NK) cellsNK cell receptors and ligandstumor immune surveillance

Identifiers

PMID32019260
PMCPMC7037299
OpenAlexW3004222930

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.