Evidence map›Paper›PMID 29527223›Full record

ArticleFrontiers in biology2017

PTEN at the interface of immune tolerance and tumor suppression.

Andrew Brandmaier, Sheng-Qi Hou, Sandra Demaria, Silvia C Formenti, Wen H Shen

Abstract read
In one paragraph

Article in Frontiers in biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 25 citations in OpenAlex.

  1. Phase II Trial of IL-12 Plasmid Transfection and PD-1 Blockade in Immunologically Quiescent Melanoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Trial
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  11. Cancers · 2019
    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

5 authors at 1 institution in 1 country.

Andrew BrandmaierDepartment of Radiation Oncology, Weill Cornell Medicine, Cornell University, New York, NY 10065, USA.
Sheng-Qi HouDepartment of Radiation Oncology, Weill Cornell Medicine, Cornell University, New York, NY 10065, USA.
Sandra DemariaDepartment of Radiation Oncology, Weill Cornell Medicine, Cornell University, New York, NY 10065, USA.
Silvia C FormentiDepartment of Radiation Oncology, Weill Cornell Medicine, Cornell University, New York, NY 10065, USA.
Wen H ShenDepartment of Radiation Oncology, Weill Cornell Medicine, Cornell University, New York, NY 10065, USA.
Cornell University · US

Funding

Role of PTEN in Mitosis and Chromosome StabilityR01GM100478 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI SHEN, WEN H. · 2012 to 2020
$2.9M
NIGMS NIH HHS R01 GM100478
6 · The paper itself

Abstract

backgroundPTEN is well known to function as a tumor suppressor that antagonizes oncogenic signaling and maintains genomic stability. The

objectiveTo understand the multifaceted functions of PTEN as both a tumor suppressor and an immune regulator.

methodsThis review will summarize the emerging knowledge of PTEN function in cancer immunoediting. In addition, the mechanisms underlying functional integration of various PTEN pathways in regulating cancer evolution and tumor immunity will be highlighted.

resultsRecent preclinical and clinical studies revealed the essential role of PTEN in maintaining immune homeostasis, which significantly expands the repertoire of PTEN functions. Mechanistically, aberrant PTEN signaling alters the interplay between the immune system and tumors, leading to immunosuppression and tumor escape.

conclusionRational design of personalized anti-cancer treatment requires mechanistic understanding of diverse PTEN signaling pathways in modulation of the crosstalk between tumor and immune cells.

Indexed as

epigenomegenomemetabolismphosphoinositide 3-kinasePTENregulatory T cells

Identifiers

PMID29527223
PMCPMC5841164
OpenAlexW2593732386

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.