Evidence map›Paper›PMID 29064420›Full record

ReviewInternational journal of molecular sciences2017

Immunogenomic Classification of Colorectal Cancer and Therapeutic Implications.

Jessica Roelands, Peter J K Kuppen, Louis Vermeulen, Cristina Maccalli, Julie Decock, Ena Wang, Francesco M Marincola, Davide Bedognetti, Wouter Hendrickx

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
–field-weighted citation impact
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

79 citing papers in PubMed.

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  19. Iron metabolism in colorectal cancer: a balancing act.Cellular oncology (Dordrecht, Netherlands) · 2023
    Review
  20. Article

19 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

9 authors.

Jessica RoelandsTumor Biology, Immunology, and Therapy Section, Immunology, Inflammation, and Metabolism Department, Division of Translational Medicine, Sidra Medical and Research Center, PO Box 26999 Doha, Qatar. jroelands@sidra.org.ORCID 0000-0003-3631-2041
Peter J K KuppenDepartment of Surgery, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands. P.J.K.Kuppen@lumc.nl.ORCID 0000-0002-0294-3251
Louis VermeulenAcademic Medical Center Amsterdam, Center for Experimental Molecular Medicine, 1105AZ Amsterdam, The Netherlands. l.vermeulen@amc.uva.nl.
Cristina MaccalliTumor Biology, Immunology, and Therapy Section, Immunology, Inflammation, and Metabolism Department, Division of Translational Medicine, Sidra Medical and Research Center, PO Box 26999 Doha, Qatar. cmaccalli@sidra.org.
Julie DecockQatar Biomedical Research Institute, Hamad Bin Khalifa University, Qatar Foundation, PO Box 5825 Doha, Qatar. jdecock@hbku.edu.qa.ORCID 0000-0002-4409-100X
Ena WangOffice of the Chief Research Officer (CRO), Sidra Medical and Research Center, PO Box 26999 Doha, Qatar. ewang@sidra.org.
Francesco M MarincolaOffice of the Chief Research Officer (CRO), Sidra Medical and Research Center, PO Box 26999 Doha, Qatar. francesco.marincola@abbvie.com.
Davide BedognettiTumor Biology, Immunology, and Therapy Section, Immunology, Inflammation, and Metabolism Department, Division of Translational Medicine, Sidra Medical and Research Center, PO Box 26999 Doha, Qatar. dbedognetti@sidra.org.
Wouter HendrickxTumor Biology, Immunology, and Therapy Section, Immunology, Inflammation, and Metabolism Department, Division of Translational Medicine, Sidra Medical and Research Center, PO Box 26999 Doha, Qatar. whendrickx@sidra.org.ORCID 0000-0002-7649-5092

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The immune system has a substantial effect on colorectal cancer (CRC) progression. Additionally, the response to immunotherapeutics and conventional treatment options (e.g., chemotherapy, radiotherapy and targeted therapies) is influenced by the immune system. The molecular characterization of colorectal cancer (CRC) has led to the identification of favorable and unfavorable immunological attributes linked to clinical outcome. With the definition of consensus molecular subtypes (CMSs) based on transcriptomic profiles, multiple characteristics have been proposed to be responsible for the development of the tumor immune microenvironment and corresponding mechanisms of immune escape. In this review, a detailed description of proposed immune phenotypes as well as their interaction with different therapeutic modalities will be provided. Finally, possible strategies to shift the CRC immune phenotype towards a reactive, anti-tumor orientation are proposed per CMS.

Indexed as

Colorectal NeoplasmsHumansImmune SystemImmunotherapyLymphocytes, Tumor-InfiltratingNeoplasm MetastasisTumor Microenvironmentcolorectal cancercombination therapyconsensus molecular subtypesimmune contextureimmunologic constant of rejectionimmunotherapytumor microenvironment

Identifiers

PMID29064420
PMCPMC5666908

What OpenQuestion holds

Textmetadata
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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.