Zhengdeng Lei, PhD

Zhengdeng Lei, PhD

2009 - Present Research Fellow at Duke-NUS, Singapore
2007 - 2009 High Throughput Computational Analyst, Memorial Sloan-Kettering Cancer Center, New York
2003 - 2007 PhD, Bioinformatics, University of Illinois at Chicago

Saturday, March 10, 2012

Tamoxifen

D subtype == LumA  response to Tamoxifen

Definition of Clinically Distinct Molecular Subtypes in
Estrogen Receptor–Positive Breast Carcinomas Through
Genomic Grade



http://www.biomedcentral.com/1755-8794/2/37

Gene expression profiling identifies activated growth factor signaling in poor prognosis (Luminal-B) estrogen receptor positive breast cancer

http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE6532

Sherene Loi, from the Peter MacCallum Cancer Centre, Melbourne, worked with a team of Australian and Belgian researchers to investigate the differences between those estrogen receptor positive (ER+) cancers that respond well to tamoxifen (luminal-A) and those that do not (luminal-B). She said, “This is the first study specifically investigating the biology of the luminal-B, ER+ breast cancer subtype. We propose that activation of GF signaling contributes to this highly proliferative, relatively tamoxifen-insensitive, phenotype and that this exists independently of HER2 overexpression. Targeting this pathway and its upstream mediators could prove to be a useful therapeutic strategy


http://www.sciencedaily.com/releases/2009/06/090623215852.htm



and
http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE2990

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