Evidence map›Paper›PMID 24413078›Full record

ReviewOncogene2014

Stress signaling and the shaping of the mammary tissue in development and cancer.

A Avivar-Valderas, H C Wen, J A Aguirre-Ghiso

Open access · bronzeAbstract readReview
In one paragraph

Review in Oncogene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.9field-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

15 citing papers in PubMed, 33 citations in OpenAlex.

  1. Immune Cell Contribution to Mammary Gland Development.Journal of mammary gland biology and neoplasia · 2024
    Review
  2. Article
  3. The need to study human milk as a biological system.The American journal of clinical nutrition · 2021
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. The cJUN NHCell death and differentiation · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. MiR-491 attenuates cancer stem cells-like properties of hepatocellular carcinoma by inhibition of GIT-1/NF-κB-mediated EMT.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  14. Article
  15. 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

3 authors at 1 institution in 1 country.

A Avivar-Valderas1] Division of Hematology and Oncology, Department of Medicine, Mount Sinai School of Medicine, New York, NY, USA [2] Department of Otolaryngology, Mount Sinai School of Medicine, New York, NY, USA [3] Tisch Cancer Institute, Mount Sinai School of Medicine, New York, NY, USA.
H C Wen1] Tisch Cancer Institute, Mount Sinai School of Medicine, New York, NY, USA [2] Department of Oncological Sciences, Mount Sinai School of Medicine, New York, NY, USA.
J A Aguirre-Ghiso1] Division of Hematology and Oncology, Department of Medicine, Mount Sinai School of Medicine, New York, NY, USA [2] Department of Otolaryngology, Mount Sinai School of Medicine, New York, NY, USA [3] Tisch Cancer Institute, Mount Sinai School of Medicine, New York, NY, USA [4] Black Family Stem Cell Institute, Mount Sinai School of Medicine, New York, NY, USA.
Icahn School of Medicine at Mount Sinai · US

Funding

Functional Determinants of Metastatic DormancyR01CA109182 · NCI · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI AGUIRRE-GHISO, JULIO A. · 2005 to 2025
$8.3M
Tumor microenvironments determing migration, dissemination and dormancyU54CA163131 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI AGUIRRE-GHISO, JULIO A., CASTRACANE, JAMES · 2011 to 2015
$3.9M
Translational Machinery in Stress Signaling and Tumor SuppressionR21ES017146 · NIEHS · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI AGUIRRE-GHISO, JULIO A., BEGLEY, THOMAS J · 2009 to 2010
$454k
NCI NIH HHS CA109182NCI NIH HHS CA163131NCI NIH HHS R01 CA109182NCI NIH HHS U54 CA163131NIEHS NIH HHS ES017146NIEHS NIH HHS R21 ES017146
6 · The paper itself

Abstract

The postnatal mammary gland develops extensively through cycles of proliferation, branching, involution and remodeling. We review recent advances made in the field of stress signaling pathways and its roles in mammary gland organogenesis, how they contribute to normal organ specification and homeostasis and how its subversion by oncogenes leads to cancer. We analyze stress signaling in mammary gland biology taking into account the interrelationship with the extracellular matrix and adhesion signaling during morphogenesis. By integrating the information gathered from in vivo and three dimensional in vitro organogenesis studies, we review the novel contribution of p38(SAPK), c-Jun NH2-terminal kinase and PKR-like endoplasmic reticulum kinase (PERK) signaling pathways to the timely activation of cell death, correct establishment of polarity and growth arrest and autophagy, respectively. We also review the evidence supporting that the activation of the aforementioned stress kinases maintain breast acinar structures as part of a tumor suppressive program and that its deregulation is commonplace during breast cancer initiation.

Indexed as

Mammary Glands, HumanAnimalsBreast NeoplasmsFemaleHumansMorphogenesisSignal Transduction

Identifiers

PMID24413078
PMCPMC4096615
OpenAlexW2014324163

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.