Evidence map›Paper›PMID 25595911›Full record

ArticleOncotarget2015

CD80-CD28 signaling controls the progression of inflammatory colorectal carcinogenesis.

Marco Scarpa, Paola Brun, Melania Scarpa, Susan Morgan, Andrea Porzionato, Andromachi Kotsafti, Marina Bortolami, Andrea Buda, Renata D'Incà, Veronica Macchi and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.0field-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

17 citing papers in PubMed, 26 citations in OpenAlex.

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  14. Disequilibrium in the CD8Digestive diseases and sciences · 2017
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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

16 authors at 4 institutions in 2 countries.

Marco ScarpaOncological Surgery Unit, Veneto Institute of Oncology IOV - IRCCS, Padova 35128, Italy.
Paola BrunDepartment of Molecular Medicine, University of Padova, Padova 35128, Italy.
Melania ScarpaOncological Surgery Unit, Veneto Institute of Oncology IOV - IRCCS, Padova 35128, Italy.
Susan MorganDepartment of Histopathology, Sheffield Teaching Hospitals, Sheffield S10 2JF, UK.
Andrea PorzionatoDepartment of Molecular Medicine, University of Padova, Padova 35128, Italy.
Andromachi KotsaftiOncological Surgery Unit, Veneto Institute of Oncology IOV - IRCCS, Padova 35128, Italy.
Marina BortolamiDepartment of Surgery Oncology and Gastroenterology, University of Padova, Padova 35128, Italy.
Andrea BudaDepartment of Surgery Oncology and Gastroenterology, University of Padova, Padova 35128, Italy.
Renata D'IncàDepartment of Surgery Oncology and Gastroenterology, University of Padova, Padova 35128, Italy.
Veronica MacchiDepartment of Molecular Medicine, University of Padova, Padova 35128, Italy.
Giacomo C SturnioloDepartment of Surgery Oncology and Gastroenterology, University of Padova, Padova 35128, Italy.
Massimo RuggeDepartment of Medicine, University of Padova, Padova 35128, Italy.
Romeo BardiniDepartment of Surgery Oncology and Gastroenterology, University of Padova, Padova 35128, Italy.
Ignazio CastagliuoloDepartment of Molecular Medicine, University of Padova, Padova 35128, Italy.
Imerio AngrimanDepartment of Surgery Oncology and Gastroenterology, University of Padova, Padova 35128, Italy.
Carlo CastoroOncological Surgery Unit, Veneto Institute of Oncology IOV - IRCCS, Padova 35128, Italy.
University of Padua · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITIstituto Oncologico Veneto · ITSheffield Teaching Hospitals NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In patients with ulcerative colitis (UC) the cumulative risk of colon cancer is lower than the actual rate of dysplasia suggesting an efficient immune surveillance mechanism. Since the co-stimulatory molecule CD80 is overexpressed in dysplastic colonic mucosa of UC patients and T-cell activation entails effective costimulation, we aimed to evaluate the functional implication of CD80 signaling in colonic UC-associated carcinogenesis. In humans, we observed that the percentage of CD80+ and HLA-A+ IEC was increased in the dysplastic colonic mucosa of UC patients. In vitro, IEC activated CD8+ T-cells through a CD80-dependent pathway. Finally, in the AOM/DSS-induced colonic adenocarcinoma model CD80 signaling inhibition significantly increased the frequency and extension of high-grade dysplasia, whereas enhancing CD80 activity with an anti-CTLA4 antibody significantly decreased colonic dysplasia. In conclusion, CD80 signaling between IEC and T-cells represents a key factor controlling the progression from low to high grade dysplasia in inflammatory colonic carcinogenesis.

Indexed as

AnimalsAntigen PresentationB7-1 AntigenCD28 AntigensColitis, UlcerativeColonic NeoplasmsDisease ProgressionHumansLymphocyte ActivationMaleMiceMice, Inbred C57BLSignal TransductionT-LymphocytesB7-1 AntigenCD28 Antigensantigen presenting cellsCD8+ T cellscolorectal carcinogenesisintestinal epithelial cellsulcerative colitis

Identifiers

PMID25595911
PMCPMC4652987
OpenAlexW1900410293

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.