Evidence map›Paper›PMID 30463850›Full record

ReviewClinical cancer research : an official journal of the American Association for Cancer Research2019

Biological Consequences of MHC-II Expression by Tumor Cells in Cancer.

Margaret L Axelrod, Rebecca S Cook, Douglas B Johnson, Justin M Balko

Open access · bronzeAbstract readReview
In one paragraph

Review in Clinical cancer research : an official journal of the American Association for Cancer Research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 318 papers.

0numbers the graph read from it
0cells of the map it votes in
318citing papers in PubMed
9.3field-weighted citation impact, top 1% 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

318 citing papers in PubMed, 487 citations in OpenAlex.

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258 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

4 authors at 1 institution in 1 country.

Margaret L AxelrodDepartment of Medicine, Vanderbilt University Medical Center, Vanderbilt University, Nashville, Tennessee.
Rebecca S CookCancer Biology Graduate Program, Vanderbilt University, Nashville, Tennessee.
Douglas B JohnsonDepartment of Medicine, Vanderbilt University Medical Center, Vanderbilt University, Nashville, Tennessee.
Justin M BalkoDepartment of Medicine, Vanderbilt University Medical Center, Vanderbilt University, Nashville, Tennessee. justin.balko@vumc.org.ORCID 0000-0002-4263-5974
Vanderbilt University · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007347 · NIGMS · VANDERBILT UNIVERSITY · PI WILLIAMS, CHRISTOPHER S. · 1985 to 2023
$26.3M
Vanderbilt Clinical Oncology Research Career Development ProgramK12CA090625 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Debra L. Friedman, Paula Jill Hurley · 2001 to 2026
$16.9M
Dusp4 in breast cancer: tumor suppressor biology and therapeutic strategiesR00CA181491 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BALKO, JUSTIN M · 2015 to 2017
$750k
NCI NIH HHS K12 CA090625NCI NIH HHS R00 CA181491NIGMS NIH HHS T32 GM007347
6 · The paper itself

Abstract

Immunotherapy has emerged as a key pillar of cancer treatment. To build upon the recent successes of immunotherapy, intense research efforts are aimed at a molecular understanding of antitumor immune responses, identification of biomarkers of immunotherapy response and resistance, and novel strategies to circumvent resistance. These studies are revealing new insight into the intricacies of tumor cell recognition by the immune system, in large part through MHCs. Although tumor cells widely express MHC-I, a subset of tumors originating from a variety of tissues also express MHC-II, an antigen-presenting complex traditionally associated with professional antigen-presenting cells. MHC-II is critical for antigen presentation to CD4

Indexed as

Disease SusceptibilityGene ExpressionAnimalsAntigen PresentationAntigen-Presenting CellsBiomarkersCD4-Positive T-LymphocytesDisease ManagementDisease Models, AnimalGene Expression Regulation, NeoplasticHistocompatibility Antigens Class IHistocompatibility Antigens Class IIHumansImmunotherapyNeoplasmsSignal TransductionBiomarkersHistocompatibility Antigens Class IHistocompatibility Antigens Class II

Identifiers

PMID30463850
PMCPMC6467754
OpenAlexW2900499839

What OpenQuestion holds

Textmetadata
LicenceTDM
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.