The Lung Pathology and Molecular Analysis Core (Core B) provides a powerful combination of experiencedand capable personnel whose primary role is to provide state of the art service and support to the researchinvestigators. To do this, the Core provides the technology and technical expertise to effectively supplementthe studies in lung cancer pathology, protein analysis, and microscopy described in this proposal. The majorobjectives of this core are to (1) facilitate the acquisition, preservation, analysis, and dispersal of clinicalsamples, (2) provide accurate histopathologic characterization of tumor tissues for all project investigators,(3) allow access to state-of-the-art analytic protein chemistry and proteomics resources for use in theidentification, quantitation, and detailed structural characterization of proteins and protein complexes, and (4)provide cutting-edge microscopy and imaging tools to ensure optimal visualization and analysis of cellularprocesses. Specifically, Lung Pathology will develop and maintain a large repository of well-preserved, well-characterizedtissue specimens obtained from lung cancer patients that are receiving care or evaluation atEmory University, or are participating in the Neoadjuvant Trial of Chemotherapy Hope (NATCH), to developunbiased comprehensive histologic characterization of the tissue samples used in each of the P-01 projects.This Core also offers reliable centralized laboratory services to the investigators with respect to tissuesamples including state-of-the-art examination of immunohistochemical stains, in-situ hybridization microdissection,and other techniques. It also serves as an important central database management resource tomaintain a comprehensive prospective, interactive database to provide access to patient demographic dataas well as detailed clinical pathologic data from patients with lung cancer. The protein analysis branch willprovide critical access to state-of-the-art analytical protein chemistry and proteomics resources for use in theidentification, quantitation, and detailed structural characterization of proteins and protein complexes asneeded. Lastly, the imaging facility will provide the necessary microscopy tools and technical expertise tovisualize the biological processes described in this application. Moreover, it will employ sophisticated imageanalysis tools for image processing and accurate quantitative analyses. Taken together, the Lung Pathologyand Molecular Analysis Core serves as a critical resource that will facilitate scientific advancement throughlung pathology, protein-based initiatives, and microscopic analysis of cellular signaling pathways.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
1P01CA116676-01A1
Application #
7109522
Study Section
Subcommittee G - Education (NCI)
Project Start
2006-01-01
Project End
2010-12-31
Budget Start
2006-01-01
Budget End
2007-05-31
Support Year
1
Fiscal Year
2006
Total Cost
$108,790
Indirect Cost
Name
Emory University
Department
Type
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Liu, Fakeng; Liu, Yuan; Liu, Xiuju et al. (2018) Inhibition of IGF1R enhances 2-deoxyglucose in the treatment of non-small cell lung cancer. Lung Cancer 123:36-43
Li, Zenggang; Ivanov, Andrei A; Su, Rina et al. (2017) The OncoPPi network of cancer-focused protein-protein interactions to inform biological insights and therapeutic strategies. Nat Commun 8:14356
Zhang, Jun; Nannapaneni, Sreenivas; Wang, Dongsheng et al. (2017) Phenformin enhances the therapeutic effect of selumetinib in KRAS-mutant non-small cell lung cancer irrespective of LKB1 status. Oncotarget 8:59008-59022
Xiong, Fei; Jiang, Miao; Chen, Meijuan et al. (2017) Study on Inhibitory Effect of MaiMenDong Decoction and WeiJing Decoction Combination with Cisplatin on NCI-A549 Xenograft in Nude Mice and Its Mechanism. J Cancer 8:2449-2455
Gilbert-Ross, Melissa; Konen, Jessica; Koo, Junghui et al. (2017) Targeting adhesion signaling in KRAS, LKB1 mutant lung adenocarcinoma. JCI Insight 2:e90487
Sun, Linlin; Liu, Xiuju; Fu, Haian et al. (2016) 2-Deoxyglucose Suppresses ERK Phosphorylation in LKB1 and Ras Wild-Type Non-Small Cell Lung Cancer Cells. PLoS One 11:e0168793
Jin, Rui; Zhou, Wei (2016) TIF-IA: An oncogenic target of pre-ribosomal RNA synthesis. Biochim Biophys Acta 1866:189-196
Liu, Fakeng; Jin, Rui; Liu, Xiuju et al. (2016) LKB1 promotes cell survival by modulating TIF-IA-mediated pre-ribosomal RNA synthesis under uridine downregulated conditions. Oncotarget 7:2519-31
Chen, Zhengjia; Chen, Xinjia (2015) Rigorous Error Control Methods for Estimating Means of Bounded Random Variables. J Stat Plan Inference 157-158:54-76
Mao, Kaisheng; Liu, Fakeng; Liu, Xiuju et al. (2015) Re-expression of LKB1 in LKB1-mutant EKVX cells leads to resistance to paclitaxel through the up-regulation of MDR1 expression. Lung Cancer 88:131-8

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