Evidence map›Paper›PMID 37663943›Full record

ArticleWorld journal of gastrointestinal oncology2023

Potential of damage associated molecular patterns in synergising radiation and the immune response in oesophageal cancer.

Noel E Donlon, Maria Davern, Andrew Sheppard, Fiona O'Connell, Brendan Moran, Timothy S Nugent, Aisling Heeran, James J Phelan, Anshul Bhardwaj, Christine Butler and 6 more

Open access · diamondAbstract read
In one paragraph

Article in World journal of gastrointestinal oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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 1 institution in 2 countries.

Noel E DonlonCancer Immunology and Immunotherapy Group, Department of Surgery, Trinity Translational Medicine Institute and Trinity St James's Cancer Institute, Trinity College Dublin, St James's Hospital, Dublin D08, Ireland. donlonn@tcd.ie.
Maria DavernCancer Immunology and Immunotherapy Group, Department of Surgery, Trinity Translational Medicine Institute and Trinity St James's Cancer Institute, Trinity College Dublin, St James's Hospital, Dublin D08, Ireland.
Andrew SheppardCancer Immunology and Immunotherapy Group, Department of Surgery, Trinity Translational Medicine Institute and Trinity St James's Cancer Institute, Trinity College Dublin, St James's Hospital, Dublin D08, Ireland.
Fiona O'ConnellCancer Immunology and Immunotherapy Group, Department of Surgery, Trinity Translational Medicine Institute and Trinity St James's Cancer Institute, Trinity College Dublin, St James's Hospital, Dublin D08, Ireland.
Brendan MoranCancer Immunology and Immunotherapy Group, Department of Surgery, Trinity Translational Medicine Institute and Trinity St James's Cancer Institute, Trinity College Dublin, St James's Hospital, Dublin D08, Ireland.
Timothy S NugentCancer Immunology and Immunotherapy Group, Department of Surgery, Trinity Translational Medicine Institute and Trinity St James's Cancer Institute, Trinity College Dublin, St James's Hospital, Dublin D08, Ireland.
Aisling HeeranCancer Immunology and Immunotherapy Group, Department of Surgery, Trinity Translational Medicine Institute and Trinity St James's Cancer Institute, Trinity College Dublin, St James's Hospital, Dublin D08, Ireland.
James J PhelanCancer Immunology and Immunotherapy Group, Department of Surgery, Trinity Translational Medicine Institute and Trinity St James's Cancer Institute, Trinity College Dublin, St James's Hospital, Dublin D08, Ireland.
Anshul BhardwajCancer Immunology and Immunotherapy Group, Department of Surgery, Trinity Translational Medicine Institute and Trinity St James's Cancer Institute, Trinity College Dublin, St James's Hospital, Dublin D08, Ireland.
Christine ButlerCancer Immunology and Immunotherapy Group, Department of Surgery, Trinity Translational Medicine Institute and Trinity St James's Cancer Institute, Trinity College Dublin, St James's Hospital, Dublin D08, Ireland.
Narayanasamy RaviCancer Immunology and Immunotherapy Group, Department of Surgery, Trinity Translational Medicine Institute and Trinity St James's Cancer Institute, Trinity College Dublin, St James's Hospital, Dublin D08, Ireland.
Claire L DonohoeCancer Immunology and Immunotherapy Group, Department of Surgery, Trinity Translational Medicine Institute and Trinity St James's Cancer Institute, Trinity College Dublin, St James's Hospital, Dublin D08, Ireland.
Niamh Lynam-LennonCancer Immunology and Immunotherapy Group, Department of Surgery, Trinity Translational Medicine Institute and Trinity St James's Cancer Institute, Trinity College Dublin, St James's Hospital, Dublin D08, Ireland.
Stephen MaherCancer Immunology and Immunotherapy Group, Department of Surgery, Trinity Translational Medicine Institute and Trinity St James's Cancer Institute, Trinity College Dublin, St James's Hospital, Dublin D08, Ireland.
John V ReynoldsCancer Immunology and Immunotherapy Group, Department of Surgery, Trinity Translational Medicine Institute and Trinity St James's Cancer Institute, Trinity College Dublin, St James's Hospital, Dublin D08, Ireland.
Joanne LysaghtCancer Immunology and Immunotherapy Group, Department of Surgery, Trinity Translational Medicine Institute and Trinity St James's Cancer Institute, Trinity College Dublin, St James's Hospital, Dublin D08, Ireland.
Trinity College · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is an intimate crosstalk between cancer formation, dissemination, treatment response and the host immune system, with inducing tumour cell death the ultimate therapeutic goal for most anti-cancer treatments. However, inducing a purposeful synergistic response between conventional therapies and the immune system remains evasive. The release of damage associated molecular patterns (DAMPs) is indicative of immunogenic cell death and propagation of established immune responses. However, there is a gap in the literature regarding the importance of DAMP expression in oesophageal adenocarcinoma (OAC) or by immune cells themselves.

aimTo investigate the effects of conventional therapies on DAMP expression and to determine whether OAC is an immunogenic cancer.

methodsWe investigated the levels of immunogenic cell death-associated DAMPs, calreticulin (CRT) and HMGB1 using an OAC isogenic model of radioresistance. DAMP expression was also assessed directly using

resultsHypoxia in combination with nutrient deprivation significantly reduces DAMP expression by OAC cells

conclusionIn conclusion, OAC expresses an immunogenic phenotype with two distinct subgroups of high and low DAMP expressors, which correlated with tumour regression grade and lymphatic invasion. It also identifies DAMPs namely CRT and HMGB1 as potential promising biomarkers in predicting good pathological responses to conventional chemo(radio)therapies currently used in the multimodal management of locally advanced disease.

Indexed as

CalreticulinDamage associated molecular patternsHMGB1Oesophageal adenocarcinomaRadiationT cells

Identifiers

PMID37663943
PMCPMC10473939
OpenAlexW4385712768

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.