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National Cancer Institute - NCI Division of Cancer Treatment and ...

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significance <strong>of</strong> Akt activation in NSCLC<br />

tumors. Collaboration <strong>of</strong> Drs. Joanna<br />

Shih, BRB, Jin Jen, CCR Laboratory <strong>of</strong><br />

Population Genetics, <strong>and</strong> Phillip A.<br />

Dennis, CCR <strong>Cancer</strong> Therapeutics Branch.<br />

■ Ingenuity network assisted transcription<br />

pr<strong>of</strong>iling: identification <strong>of</strong> a new pharmacological<br />

mechanism for MK886.<br />

Collaboration <strong>of</strong> Drs. Shih, BRB, <strong>and</strong><br />

Anatoly L. Mayburd, CCR Cell <strong>and</strong><br />

<strong>Cancer</strong> Biology Branch.<br />

■ Desmoglein 3 as a prognostic indicator<br />

in lung cancer. Collaborators are<br />

Drs. Shih, BRB, <strong>and</strong> Jen.<br />

■ Cross-species comparisons <strong>of</strong> mouse<br />

mammary tumor models <strong>and</strong> human<br />

breast cancer by expression pr<strong>of</strong>iling:<br />

identification <strong>of</strong> luminal <strong>and</strong> basal<br />

phenotypes <strong>and</strong> a conserved gene<br />

signature discriminating estrogenreceptor-positive<br />

from estrogenreceptor-negative<br />

tumors. Collaboration<br />

<strong>of</strong> Drs. Shih <strong>and</strong> Jeff Green, CCR<br />

Laboratory <strong>of</strong> Cell Regulation <strong>and</strong><br />

Carcinogenesis.<br />

■ Histological staining method preparatory<br />

to laser capture microdissection<br />

significantly affects detection <strong>of</strong> mRNAs<br />

in microarray hybridization. Collaboration<br />

<strong>of</strong> Drs. Shih <strong>and</strong> Frederic Mushinski,<br />

CCR Laboratory <strong>of</strong> Genetics.<br />

■ Identifying the sequential alterations<br />

<strong>of</strong> the genome, transcriptome, <strong>and</strong><br />

proteome that define the transformation<br />

<strong>of</strong> normal colon epithelium <strong>and</strong><br />

the progression from adenomas to<br />

invasive disease. Collaboration <strong>of</strong><br />

Drs. Lisa McShane <strong>and</strong> Ed Korn, BRB,<br />

with Thomas Ried <strong>and</strong> others <strong>of</strong><br />

the CCR <strong>Cancer</strong> Genomics Section<br />

<strong>of</strong> the Genetics Branch.<br />

■ Effectiveness <strong>of</strong> gene expression pr<strong>of</strong>iling<br />

for response prediction <strong>of</strong> rectal<br />

adenocarcinomas in preoperative<br />

chemoradiotherapy. Collaboration <strong>of</strong><br />

Drs. Sudhir Varma <strong>and</strong> Richard Simon,<br />

BRB, with Ried <strong>and</strong> his colleagues.<br />

■ Selective utilization <strong>of</strong> the Wnt/<br />

b-catenin signaling pathway <strong>and</strong><br />

aneuploidy-dependent massive<br />

deregulation <strong>of</strong> the cellular transcriptome<br />

in human rectal carcinomas.<br />

Collaboration <strong>of</strong> Drs. Varma <strong>and</strong> Simon,<br />

BRB, with Ried <strong>and</strong> colleagues.<br />

Dr. Thomas Ried, CCR Genetics Branch.<br />

Network mapping <strong>of</strong> genes involved in rectal tumorigenesis. Shades <strong>of</strong> red<br />

indicate genes with five-fold or greater expression in the tumors; shades <strong>of</strong><br />

green indicate genes with a more than five-fold decrease in expression in<br />

the tumors relative to the normal rectal mucosa.<br />

B I O M E T R I C R E S E A R C H B R A N C H ■ 15

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