Evidence map›Paper›PMID 26976639›Full record

ArticleMolecular and cellular biology2016

Phosphatidylinositol 3-Kinase/Akt Mediates Integrin Signaling To Control RNA Polymerase I Transcriptional Activity.

Chuanyue Wu, Jin You, Jijun Fu, Xingshun Wang, Yandong Zhang

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. Effects ofBiology · 2026
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  8. Identification and Characterization of the Wilms Tumor Cancer Stem Cell.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  9. Article
  10. Review
  11. Review
  12. mTOR Signaling Components in Tumor Mechanobiology.International journal of molecular sciences · 2022
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
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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 2 countries.

Chuanyue WuDepartment of Biology, South University of Science and Technology of China, Shenzhen, China Shenzhen Key Laboratory of Cell Microenvironment, South University of Science and Technology, Shenzhen, China Department of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA wucy@sustc.edu.cn zhangyd@sustc.edu.cn.
Jin YouDepartment of Biology, South University of Science and Technology of China, Shenzhen, China.
Jijun FuDepartment of Biology, South University of Science and Technology of China, Shenzhen, China.
Xingshun WangDepartment of Biology, South University of Science and Technology of China, Shenzhen, China.
Yandong ZhangDepartment of Biology, South University of Science and Technology of China, Shenzhen, China wucy@sustc.edu.cn zhangyd@sustc.edu.cn.
Southern University of Science and Technology · CN

Funding

Signaling Mechanisms of Focal Adhesion Protein Kindlin-2 in ChondrogenesisR01AR068950 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HUANG, JIAN, WU, CHUANYUE · 2015 to 2019
$2.2M
A novel kindlin-2 regulatory pathway in bone remodelingR21AR064874 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WU, CHUANYUE, XIAO, GUOZHI · 2015 to 2016
$383k
NIAMS NIH HHS R01 AR068950NIAMS NIH HHS R21 AR064874
6 · The paper itself

Abstract

RNA polymerase I-mediated rRNA production is a key determinant of cell growth. Despite extensive studies, the signaling pathways that control RNA polymerase I-mediated rRNA production are not well understood. Here we provide original evidence showing that RNA polymerase I transcriptional activity is tightly controlled by integrin signaling. Furthermore, we show that a signaling axis consisting of focal adhesion kinase (FAK), Src, phosphatidylinositol 3-kinase (PI3K), Akt, and mTOR mediates the effect of integrin signaling on rRNA transcription. Additionally, we show that in kindlin-2 knockout mouse embryonic fibroblasts, overactivation of Ras, Akt, and Src can successfully rescue the defective RNA polymerase I activity induced by the loss of kindlin-2. Finally, through experiments with inhibitors of FAK, Src, and PI3K and rescue experiments in MEFs, we found that the FAK/Src/PI3K/Akt signaling pathway to control rRNA transcription is linear. Collectively, these studies reveal, for the first time, a pivotal role of integrin signaling in regulation of RNA polymerase I transcriptional activity and shed light on the downstream signaling axis that participates in regulation of this key aspect of cell growth.

Indexed as

AnimalsCell LineCell ProliferationFibroblastsFocal Adhesion Kinase 1IntegrinsMicePhosphatidylinositol 3-KinaseProto-Oncogene Proteins c-aktRNA Polymerase IRNA, RibosomalSignal Transductionsrc-Family KinasesTOR Serine-Threonine KinasesTranscription, GeneticFocal Adhesion Kinase 1IntegrinsmTOR protein, mousePhosphatidylinositol 3-KinaseProto-Oncogene Proteins c-aktPtk2 protein, mouseRNA Polymerase IRNA, Ribosomalsrc-Family KinasesTOR Serine-Threonine Kinases

Identifiers

PMID26976639
PMCPMC4859695
OpenAlexW2346168689

What OpenQuestion holds

Textmetadata
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.