Evidence map›Paper›PMID 28602818›Full record

ReviewJournal of molecular biology2017

Cell Cycle Control by PTEN.

Andrew Brandmaier, Sheng-Qi Hou, Wen H Shen

Open access · greenAbstract readReview
In one paragraph

Review in Journal of molecular biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
4.5field-weighted citation impact, top 4% 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, 101 citations in OpenAlex.

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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

3 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.
Wen H ShenDepartment of Radiation Oncology, Weill Cornell Medicine, Cornell University, New York, NY 10065, USA. Electronic address: wes2007@med.cornell.edu.
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

Continuous and error-free chromosome inheritance through the cell cycle is essential for genomic stability and tumor suppression. However, accumulation of aberrant genetic materials often causes the cell cycle to go awry, leading to malignant transformation. In response to genotoxic stress, cells employ diverse adaptive mechanisms to halt or exit the cell cycle temporarily or permanently. The intrinsic machinery of cycling, resting, and exiting shapes the cellular response to extrinsic stimuli, whereas prevalent disruption of the cell cycle machinery in tumor cells often confers resistance to anticancer therapy. Phosphatase and tensin homolog (PTEN) is a tumor suppressor and a guardian of the genome that is frequently mutated or deleted in human cancer. Moreover, it is increasingly evident that PTEN deficiency disrupts the fundamental processes of genetic transmission. Cells lacking PTEN exhibit cell cycle deregulation and cell fate reprogramming. Here, we review the role of PTEN in regulating the key processes in and out of cell cycle to optimize genomic integrity.

Indexed as

Cell Cycle CheckpointsAnimalsCarcinogenesisHumansNeoplasmsPTEN PhosphohydrolasePTEN Phosphohydrolasecell cyclegenetic transmissionPTENquiescencesenescence

Identifiers

PMID28602818
PMCPMC5659283
OpenAlexW2622857043

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.