Evidence map›Paper›PMID 26869349›Full record

ArticleNature communications2016

The mRNA-edited form of GABRA3 suppresses GABRA3-mediated Akt activation and breast cancer metastasis.

Kiranmai Gumireddy, Anping Li, Andrew V Kossenkov, Masayuki Sakurai, Jinchun Yan, Yan Li, Hua Xu, Jian Wang, Paul J Zhang, Lin Zhang and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 138 papers.

0numbers the graph read from it
0cells of the map it votes in
138citing papers in PubMed
7.1field-weighted citation impact, top 3% 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

138 citing papers in PubMed, 211 citations in OpenAlex.

  1. Trial
  2. Acta pharmaceutica Sinica. B · 2026
    Review
  3. Review
  4. Article
  5. Review
  6. RNA modifications in cancer and their detection: a review.Japanese journal of clinical oncology · 2026
    Review
  7. Article
  8. Two codes of RNA editing by deamination in human diseases.Experimental & molecular medicine · 2026
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. The Functional Interplay among GAD2, GABRG2, and CACNA1G Genes in Cancers.Asian Pacific journal of cancer prevention : APJCP · 2025
    Review
  19. Review
  20. Review

78 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

13 authors at 7 institutions in 2 countries.

Kiranmai GumireddyDepartment of Tumor Microenvironment and Metastasis, The Wistar Institute, 3601 Spruce Street, Philadelphia, Pennsylvania 19104, USA.
Anping LiDepartment of Tumor Microenvironment and Metastasis, The Wistar Institute, 3601 Spruce Street, Philadelphia, Pennsylvania 19104, USA.
Andrew V KossenkovDepartment of Tumor Microenvironment and Metastasis, The Wistar Institute, 3601 Spruce Street, Philadelphia, Pennsylvania 19104, USA.
Masayuki SakuraiDepartment of Tumor Microenvironment and Metastasis, The Wistar Institute, 3601 Spruce Street, Philadelphia, Pennsylvania 19104, USA.
Jinchun YanUniversity of Washington Medical Center, 1959 N.E. Pacific Street, Seattle, Washington 98195, USA.
Yan LiInstitute of Cancer Stem Cell, Department of Anatomy, College of Basic Medical Sciences, Dalian Medical University, No. 9 West Section Lvshun South Road, Dalian 116044, China.
Hua XuDepartment of Urology, Tongji Hospital, Tongji Medical College, Huazhong University of Sciences and Technology, Wuhan 430030, China.
Jian WangDepartment of Biliary-Pancreatic Surgery, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200127, China.
Paul J ZhangDepartment of Pathology and Laboratory Medicine, Hospital of The University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania 19104, USA.
Lin ZhangDepartment of Obstetrics and Gynecology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
Louise C ShoweDepartment of Tumor Microenvironment and Metastasis, The Wistar Institute, 3601 Spruce Street, Philadelphia, Pennsylvania 19104, USA.
Kazuko NishikuraDepartment of Tumor Microenvironment and Metastasis, The Wistar Institute, 3601 Spruce Street, Philadelphia, Pennsylvania 19104, USA.
Qihong HuangDepartment of Tumor Microenvironment and Metastasis, The Wistar Institute, 3601 Spruce Street, Philadelphia, Pennsylvania 19104, USA.
The Wistar Institute · USDalian Medical University · CNHospital of the University of Pennsylvania · USRenji Hospital · CNTongji Hospital · CNUniversity of Pennsylvania · USUniversity of Washington Medical Center · US

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
STRUCTURE AND FUNCTION OF DSRNA ADENOSINE DEAMINASER01GM040536 · NIGMS · WISTAR INSTITUTE · PI NISHIKURA, KAZUKO · 1991 to 2021
$8.1M
Control of Breast Cancer Metastasis by Epstein-Barr Virus microRNAR01CA175058 · NCI · WISTAR INSTITUTE · PI NISHIKURA, KAZUKO · 2014 to 2018
$2.0M
The epigenetic mechanism of long non-coding RNA in cancerR01CA190415 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ZHANG, LIN · 2015 to 2019
$1.8M
Defining the Molecular Mechanisms of KLF17 Regulation and Function in EMTR01CA148759 · NCI · WISTAR INSTITUTE · PI HUANG, QIHONG · 2010 to 2014
$1.7M
Integrative Approach to Comprehensive Analysis of High Throughput Data on a Cancer Center LevelR50CA211199 · NCI · WISTAR INSTITUTE · PI Andrew V Kossenkov · 2016 to 2026
$1.6M
The role of microRNA, mir-30d, in the initiation and progression of cancerR01CA142776 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ZHANG, LIN · 2010 to 2014
$1.6M
Development of circulating biomarker for lung cancerR21CA198558 · NCI · WISTAR INSTITUTE · PI SHOWE, LOUISE C. · 2016 to 2017
$460k
NCI NIH HHS CA010815NCI NIH HHS P30 CA010815NCI NIH HHS R01 CA142776NCI NIH HHS R01CA142776NCI NIH HHS R01 CA148759NCI NIH HHS R01CA148759NCI NIH HHS R01 CA175058NCI NIH HHS R01-CA175058NCI NIH HHS R01 CA190415NCI NIH HHS R01CA190415NCI NIH HHS R21 CA198558NCI NIH HHS R50 CA211199NIGMS NIH HHS R01 GM040536NIGMS NIH HHS R01-GM040536
6 · The paper itself

Abstract

Metastasis is a critical event affecting breast cancer patient survival. To identify molecules contributing to the metastatic process, we analysed The Cancer Genome Atlas (TCGA) breast cancer data and identified 41 genes whose expression is inversely correlated with survival. Here we show that GABAA receptor alpha3 (Gabra3), normally exclusively expressed in adult brain, is also expressed in breast cancer, with high expression of Gabra3 being inversely correlated with breast cancer survival. We demonstrate that Gabra3 activates the AKT pathway to promote breast cancer cell migration, invasion and metastasis. Importantly, we find an A-to-I RNA-edited form of Gabra3 only in non-invasive breast cancers and show that edited Gabra3 suppresses breast cancer cell invasion and metastasis. A-to-I-edited Gabra3 has reduced cell surface expression and suppresses the activation of AKT required for cell migration and invasion. Our study demonstrates a significant role for mRNA-edited Gabra3 in breast cancer metastasis.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsBreast NeoplasmsCase-Control StudiesCell Line, TumorCell MovementFemaleHumansMCF-7 CellsMiceNeoplasm InvasivenessNeoplasm MetastasisNeoplasm StagingNeoplasm TransplantationProportional Hazards ModelsProto-Oncogene Proteins c-aktGABRA3 protein, humanProto-Oncogene Proteins c-aktReceptors, GABA-ARNA, Messenger

Identifiers

PMID26869349
PMCPMC4754346
OpenAlexW2274759799

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.