Evidence map›Paper›PMID 28230277›Full record

ReviewJournal of cellular biochemistry2017

Immune Checkpoint Blockade Biology in Mouse Models of Glioblastoma.

Alan T Yeo, Alain Charest

Open access · greenAbstract readReview
In one paragraph

Review in Journal of cellular biochemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

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  7. Pre-clinical tumor models of primary brain tumors: Challenges and opportunities.Biochimica et biophysica acta. Reviews on cancer · 2021
    Review
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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

2 authors at 2 institutions in 1 country.

Alan T YeoSackler School of Graduate Studies, Tufts University School of Medicine, 136 Harrison Ave, Boston, Massachusetts 02111.
Alain CharestCancer Research Institute, Beth Israel Deaconess Medical Center, 330 Brookline Ave, Boston, Massachusetts 02215.ORCID 0000-0002-1548-6950
Beth Israel Deaconess Medical Center · USTufts University · US

Funding

The role of microvesicles in giloma virotherapyP01CA069246 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI CHAREST, ALAIN · 1996 to 2021
$30.9M
Transfer of microRNA regulators from glioblastoma to brain microenvironment U19CA179563 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI BREAKEFIELD, XANDRA OWENS, CHAREST, ALAIN · 2013 to 2017
$8.6M
(PQB5)Molecular Wiring and Therapeutic Targeting of EGFR and PDGFR Signaling NetwR01CA185137 · NCI · TUFTS MEDICAL CENTER · PI CHAREST, ALAIN, GYGI, STEVEN P · 2014 to 2017
$3.5M
NCI NIH HHS P01 CA069246NCI NIH HHS R01 CA185137NCI NIH HHS U19 CA179563
6 · The paper itself

Abstract

Glioblastoma Multiforme (GBM) is a highly malignant primary brain cancer that is associated with abysmal prognosis. The median survival of GBM patients is ∼15 months and there have not been any significant advance in therapies in over a decade, leaving treatment options limited. There is clearly an unmet need for GBM treatment. Immunotherapies are treatments based on usurping the power of the host's immune system to recognize and eliminate cancer cells. They have recently proven to be a successful strategy for combating a variety of cancers. Of the various types of immunotherapies, checkpoint blockade approaches have thus far produced significant clinical responses in several cancers including melanoma, non small-cell lung cancer, renal cancer, and prostate cancer. This review focuses on the biological rationale for using checkpoint blockade immunotherapeutic approaches in primary brain cancer and an up-to-date summary of current and ongoing checkpoint inhibitors-based clinical trials for malignant glioma. In addition, we expand on new concepts for further improving checkpoint blockade treatments, with a particular focus on the advantages of using genetically engineered mouse models for studies of immunotherapies in GBM. J. Cell. Biochem. 118: 2516-2527, 2017. © 2017 Wiley Periodicals, Inc.

Indexed as

Brain NeoplasmsGlioblastomaNeoplasms, ExperimentalAnimalsHumansImmunotherapyMiceCANCERCHECKPOINT INHIBITORSGENETICALLY ENGINEERED MOUSE MODELSGLIOBLASTOMA MULTIFORME

Identifiers

PMID28230277
PMCPMC5783695
OpenAlexW2590574936

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.