Laura M. Selfors

Laura M. Selfors

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Laura M. Selfors

Department of Cell Biology, Harvard Medical School, Boston, Massachusetts

Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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30 July 2009 in Nature Methods
Verified
Journal Article
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ABAmanda Birmingham
Amanda Birmingham
LSLaura M Selfors
Laura M Selfors
TFThorsten Forster
Thorsten Forster
DWDavid Wrobel
David Wrobel
CKCaleb J Kennedy
Caleb J Kennedy
CSCaroline E Shamu
Caroline E Shamu

10 August 2008 in Nature Cell Biology
Verified
Journal Article
Closed access
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KSKaylene Simpson
Kaylene Simpson
LSLaura M. Selfors
Laura M. Selfors
JBJames Bui
James Bui
ARAngela Reynolds
Angela Reynolds
DLDevin Leake
Devin Leake
JBJoan S. Brugge
Joan S. Brugge

1 February 2012 in Cancer Cell
Verified
Journal Article
Closed access
TMTaru Muranen
Taru Muranen
LSLaura M. Selfors
Laura M. Selfors
DWDevin T. Worster
Devin T. Worster
MIMarcin P. Iwanicki
Marcin P. Iwanicki
LSLoling Song
Loling Song
JBJoan Brigge
Joan Brigge

1 May 2016 in Cell Metabolism
Verified
Journal Article
Closed access
JCJonathan L Coloff
Jonathan L Coloff
JMJ Patrick Murphy
J Patrick Murphy
CBCraig R Braun
Craig R Braun
IHIsaac S Harris
Isaac S Harris
LSLaura M Shelton
Laura M Shelton
JBJoan Brigge
Joan Brigge

1 June 2018 in Cancer Cell
Verified
Journal Article
Closed access
NTNobuaki Takahashi
Nobuaki Takahashi
HCHsing-Yu Chen
Hsing-Yu Chen
IHIsaac S. Harris
Isaac S. Harris
DSDaniel G. Stover
Daniel G. Stover
LSLaura M. Selfors
Laura M. Selfors
JBJoan Brigge
Joan Brigge

6 April 2020 in Nature Communications
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Journal Article
Open access
PDF file
JRJennifer M. Rosenbluth
Jennifer M. Rosenbluth
RSRon C. J. Schackmann
Ron C. J. Schackmann
GGG. Kenneth Gray
G. Kenneth Gray
LSLaura M. Selfors
Laura M. Selfors
CLCarman Man-Chung Li
Carman Man-Chung Li
JBJoan Brigge
Joan Brigge
Recently, organoid technology has been used to generate a large repository of breast cancer organoids. Here we present an extensive evaluation of the ability of organoid culture technology to preserve complex stem/progenitor and differentiated cell types via long-term propagation of normal human mammary tissues. Basal/stem and luminal progenitor cells can differentiate in culture to generate mature basal and luminal cell types, including ER+ cells that have been challenging to maintain in culture. Cells associated with increased cancer risk can also be propagated. Single-cell analyses of matched organoid cultures and native tissues by mass cytometry for 38 markers provide a higher resolution representation of the multiple mammary epithelial cell types in the organoids, and demonstrate that protein expression patterns of the tissue of origin can be preserved in culture. These studies indicate that organoid cultures provide a valuable platform for studies of mammary differentiation, transformation, and breast cancer risk.