Evidence map›Paper›PMID 24395789›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Pttg1/securin is required for the branching morphogenesis of the mammary gland and suppresses mammary tumorigenesis.

Rashieda J Hatcher, Jie Dong, Shuang Liu, Guangxing Bian, Alejandro Contreras, Tao Wang, Susan G Hilsenbeck, Yi Li, Pumin Zhang

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. iScience · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Pituitary tumor-transforming gene-1 serves as an independent prognostic biomarker for gastric cancer.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2016
    Article
  11. Article
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

9 authors at 5 institutions in 4 countries.

Rashieda J HatcherDepartment of Molecular Physiology and Biophysics, Lester and Sue Smith Breast Center, and Department of Molecular and Cell Biology, Baylor College of Medicine, Houston, TX 77030.
Jie Dong
Shuang Liu
Guangxing Bian
Alejandro Contreras
Tao Wang
Susan G Hilsenbeck
Yi Li
Pumin Zhang
Breast Center · CHInstitute of Molecular Biology and Biophysics · RUBaylor College of Medicine · USBeijing Proteome Research Center · CNState Key Laboratory of Proteomics

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Michael M Ittmann · 2007 to 2026
$73.9M
Spindle Assembly Checkpoint, Chromosome Stability, and CancerR01CA122623 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ZHANG, PUMIN · 2008 to 2016
$2.8M
The Function of Cdc14B in DNA Damage Repair and TumorigenesisR01CA116097 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ZHANG, PUMIN · 2006 to 2015
$2.6M
Oncogene susceptibility: physiological state & breast cell differentiationR01CA124820 · NCI · BAYLOR COLLEGE OF MEDICINE · PI LI, YI · 2010 to 2014
$1.5M
NCI NIH HHS CA116097NCI NIH HHS CA122623NCI NIH HHS CA124820NCI NIH HHS CA125123NCI NIH HHS P30 CA125123NCI NIH HHS R01 CA116097NCI NIH HHS R01 CA122623NCI NIH HHS R01 CA124820
6 · The paper itself

Abstract

Pituitary tumor transforming gene 1 (Pttg1) encodes the mammalian securin, which is an inhibitor of separase (a protease required for the separation of sister chromatids in mitosis and meiosis). PTTG1 is overexpressed in a number of human cancers and has been suggested to be an oncogene. However, we found that, in Pttg1-mutant females, the mammary epithelial cells showed increased proliferation and precocious branching morphogenesis. In accord with these phenotypic changes, progesterone receptor, cyclin D1, and Mmp2 were up-regulated whereas p21 (Cdkn1a) was down-regulated. These molecular changes provide explanation for the observed developmental defects, and suggest that Pttg1 is a tumor suppressor. Indeed, mice lacking Pttg1 developed spontaneous mammary tumors. Furthermore, in human breast tumors, PTTG1 protein levels were down-regulated and the reduction was significantly correlated with the tumor grade.

Indexed as

Gene Expression Regulation, DevelopmentalGene Expression Regulation, NeoplasticAnimalsApoptosisBreast NeoplasmsCell Line, TumorCell ProliferationCell Transformation, NeoplasticChromatidsCyclin-Dependent Kinase Inhibitor p21Epithelial CellsFemaleGene Expression ProfilingHumansMammary Glands, AnimalMammary Neoplasms, AnimalCdkn1a protein, mouseCyclin-Dependent Kinase Inhibitor p21Neoplasm Proteinspituitary tumor-transforming protein 1, humanPTTG1 protein, mouseSecurin

Identifiers

PMID24395789
PMCPMC3903200
OpenAlexW2050498509

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.