Evidence map›Paper›PMID 38516270›Full record

ArticleOncoimmunology2024

Co-inhibition of TGF-β and PD-L1 pathways in a metastatic colorectal cancer mouse model triggers interferon responses, innate cells and T cells, alongside metabolic changes and tumor resistance.

Reshmi Nair, Tamsin R M Lannagan, Rene Jackstadt, Anna Andrusaite, John Cole, Caitlin Boyne, Robert J B Nibbs, Owen J Sansom, Simon Milling

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Reshmi NairSchool of infection and immunity, University of Glasgow, Glasgow, UK.
Tamsin R M LannaganCancer Research UK Scotland Institute, Glasgow, UK.
Rene JackstadtCancer Research UK Scotland Institute, Glasgow, UK.
Anna AndrusaiteSchool of infection and immunity, University of Glasgow, Glasgow, UK.
John ColeSchool of infection and immunity, University of Glasgow, Glasgow, UK.
Caitlin BoyneSchool of infection and immunity, University of Glasgow, Glasgow, UK.
Robert J B NibbsSchool of infection and immunity, University of Glasgow, Glasgow, UK.
Owen J SansomCancer Research UK Scotland Institute, Glasgow, UK.
Simon MillingSchool of infection and immunity, University of Glasgow, Glasgow, UK.
University of Glasgow · GBCancer Research UK · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is the third most prevalent cancer worldwide with a high mortality rate (20-30%), especially due to metastasis to adjacent organs. Clinical responses to chemotherapy, radiation, targeted and immunotherapies are limited to a subset of patients making metastatic CRC (mCRC) difficult to treat. To understand the therapeutic modulation of immune response in mCRC, we have used a genetically engineered mouse model (GEMM), "KPN", which resembles the human 'CMS4'-like subtype. We show here that transforming growth factor (TGF-β1), secreted by KPN organoids, increases cancer cell proliferation, and inhibits splenocyte activation

Indexed as

Colonic NeoplasmsRectal NeoplasmsAnimalsB7-H1 AntigenHumansInterferonsMiceT-Lymphocytes, CytotoxicTransforming Growth Factor betaTransforming Growth Factor beta1B7-H1 AntigenInterferonsTransforming Growth Factor betaTransforming Growth Factor beta1Check point inhibitioncolorectal cancerdrug-mediated resistanceimmunotherapymetabolismmice modelsmyeloid cellsT-lymphocytes

Identifiers

PMID38516270
PMCPMC10956632
OpenAlexW4393008446

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.