Evidence map›Paper›PMID 25043309›Full record

ArticleOncogene2015

Actin filament-associated protein 1 is required for cSrc activity and secretory activation in the lactating mammary gland.

J M Cunnick, S Kim, J Hadsell, S Collins, C Cerra, P Reiser, D C Flynn, Y Cho

Abstract read
In one paragraph

Article in Oncogene, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

8 citing papers in PubMed, 15 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

8 authors at 3 institutions in 1 country.

J M CunnickDepartment of Basic Sciences, The Commonwealth Medical College, Scranton, PA, USA.
S KimGraduate School of Medicine, The Commonwealth Medical College, Scranton, PA, USA.
J HadsellFortis Institute Scranton, Scranton, PA, USA.
S CollinsDepartment of Basic Sciences, The Commonwealth Medical College, Scranton, PA, USA.
C CerraDepartment of Pathology, Pocono Health System, East Stroudsburg, PA, USA.
P ReiserDepartment of Pathology, Pocono Health System, East Stroudsburg, PA, USA.
D C FlynnCollege of Health Science, University of Delaware, Newark, DE, USA.
Y ChoDepartment of Basic Sciences, The Commonwealth Medical College, Scranton, PA, USA.
Commonwealth Medical College · USUniversity of Delaware · USUniversity of Scranton · US

Funding

AFAP-110 regulates signals that affect F-actinR01CA060731 · NCI · WEST VIRGINIA UNIVERSITY · PI HOLT, JEFFREY T · 1999 to 2012
$3.3M
NCI NIH HHS R01 CA060731NCI NIH HHS R01CA060731-15A1
6 · The paper itself

Abstract

Actin filament-associated protein 1 (AFAP1) is an adaptor protein of cSrc that binds to filamentous actin and regulates the activity of this tyrosine kinase to affect changes to the organization of the actin cytoskeleton. In breast and prostate cancer cells, AFAP1 has been shown to regulate cellular responses requiring actin cytoskeletal changes such as adhesion, invadopodia formation and invasion. However, a normal physiologic role for AFAP1 has remained elusive. In this study, we generated an AFAP1 knockout mouse model that establishes a novel physiologic role for AFAP1 in lactation. Specifically, these animals displayed a defect in lactation that resulted in an inability to nurse efficiently. Histologically, the mammary glands of the lactating knockout mice were distinguished by the accumulation of large cytoplasmic lipid droplets in the alveolar epithelial cells. There was a reduction in lipid synthesis and the expression of lipogenic genes without a corresponding reduction in the production of β-casein, a milk protein. Furthermore, these defects were associated with histologic and biochemical signs of precocious involution. This study also demonstrated that AFAP1 responds to prolactin, a lactogenic hormone, by forming a complex with cSrc and becoming tyrosine phosphorylated. Taken together, these observations pointed to a defect in secretory activation. Certain characteristics of this phenotype mirrored the defect in secretory activation in the cSrc knockout mouse, but most importantly, the activity of cSrc in the mammary gland was reduced during early lactation in the AFAP1-null mouse and the localization of active cSrc at the apical surface of luminal epithelial cells during lactation was selectively lost in the absence of AFAP1. These data define, for the first time, the requirement of AFAP1 for the spatial and temporal regulation of cSrc activity in the normal breast, specifically for milk production.

Indexed as

AnimalsFemaleLactationMammary Glands, AnimalMiceMice, KnockoutMicrofilament Proteinssrc-Family KinasesAfap1 protein, mouseMicrofilament Proteinssrc-Family Kinases

Identifiers

PMID25043309
PMCPMC4302073
OpenAlexW2062359063

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Registered trials

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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.