Evidence map›Paper›PMID 31524634›Full record

ArticleThe Journal of clinical investigation2019

Immune overdrive signature in colorectal tumor subset predicts poor clinical outcome.

Marwan Fakih, Ching Ouyang, Chongkai Wang, Travis Yiwey Tu, Maricel C Gozo, May Cho, Marvin Sy, Jeffrey A Longmate, Peter P Lee

Open access · hybridAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
5.4field-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

55 citing papers in PubMed, 1 synthesis or guideline pooled it, 97 citations in OpenAlex.

  1. Pooled it
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  11. Ferroptosis and the tumor microenvironment.Journal of experimental & clinical cancer research : CR · 2024
    Review
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  19. International journal of molecular sciences · 2023
    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

9 authors at 3 institutions in 1 country.

Marwan FakihDepartment of Medical Oncology and Therapeutics Research, and.
Ching OuyangCenter for Informatics, City of Hope National Medical Center, Duarte, California, USA.
Chongkai WangDepartment of Medical Oncology and Therapeutics Research, and.
Travis Yiwey TuDepartment of Immuno-Oncology, and.
Maricel C GozoDepartment of Immuno-Oncology, and.
May ChoDepartment of Medical Oncology and Therapeutics Research, and.
Marvin SyDepartment of Medical Oncology and Therapeutics Research, and.
Jeffrey A LongmateDepartment of Computational and Quantitative Medicine.
Peter P LeeDepartment of Immuno-Oncology, and.
Therapeutics Clinical Research · USCity Of Hope National Medical Center · USQuantitative BioSciences · US

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI XIWEI WU · 1985 to 2026
$86.3M
NCI NIH HHS P30 CA033572
6 · The paper itself

Abstract

The prognostic value of immune cell infiltration within the tumor microenvironment (TME) has been extensively investigated via histological and genomic approaches. Based on the positive prognostic value of T cell infiltration, Immunoscore has been developed and validated for predicting risk of recurrence for colorectal cancer (CRC). Also, association between a consensus T helper 1 (Th-1) immune response and favorable clinical outcomes has been observed across multiple cancer types. Here, we reanalyzed public genomic data sets from The Cancer Genome Atlas (TCGA) and NCBI Gene Expression Omnibus (NCBI-GEO) and performed multispectral immunohistochemistry (IHC) on a cohort of colorectal tumors. We identified and characterized a risk group, representing approximately 10% of CRC patients, with high intratumoral CD8+ T cell infiltration, but poor prognosis. These tumors included both microsatellite instable (MSI) and stable (MSS) phenotypes and had a high density of tumor-associated macrophages (TAMs) that expressed CD274 (programmed death-ligand 1 [PD-L1]), TGF-β activation, and an immune overdrive signature characterized by the overexpression of immune response and checkpoint genes. Our findings illustrate that CRC patients may have poor prognosis despite high CD8+ T cell infiltration and provide CD274 as a simple biomarker for identifying these patients.

Indexed as

B7-H1 AntigenBiomarkers, TumorCD8 AntigensCD8-Positive T-LymphocytesCohort StudiesColorectal NeoplasmsDatabases, GeneticGene ExpressionHumansImmunohistochemistryLymphocytes, Tumor-InfiltratingMacrophagesMelanomaMicrosatellite InstabilityPhenotypePrognosisB7-H1 AntigenBiomarkers, TumorCD274 protein, humanCD8 antigen, alpha chainCD8 AntigensCancerImmunologyMacrophagesOncologyT cells

Identifiers

PMID31524634
PMCPMC6763253
OpenAlexW2972895479

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.