The Genomics & Bioinformatics Group (GBG) is undertaking what has been characterized by others as a forerunner of the NCI/NHGRI Human Genome Atlas project (TCGA). Whereas TCGA aims at molecular profiling of clinical tumors at the DNA, RNA, and chromosomal levels, the GBG's work aims at a broader profiling at the DNA, RNA, protein, chromosomal, functional, and pharmacological levels - but in the logistically simpler, more homogeneous, more reproducible context of human cell lines, rather than clinical tumors. More specifically, we have established a set of collaborations for molecular profiling of selected drug-resistant cell lines and also the panel of 60 human cancer cell lines (the NCI-60) used by the NCI Developmental Therapeutics Program to screen >100,000 compounds and natural products for anticancer activity. The ultimate aim is to discover new drugs and biomarkers for targeted, personalized treatment of cancer. In that aim, we are also 'setting the table' for other researchers by producing molecular profile databases and bioinformatic software tools that are being used by thousands of laboratories around the world. That is, we are providing infrastructure for post-genomic biomedical research at the same time as we are pursuing translational goals related to drugs and biomarkers for personalization of cancer therapy. That enterprise yields a number of types of contributions: * Molecular profile databases used by large numbers of laboratories and investigators (4 of our publications presenting the data have each generated more than 400 literature citations to date). * Bioinformatic computer tools and resources (the Miner Suite) that we originally programmed because we needed them but that we also make freely available on our web site (http://discover.nci.nih.gov). The manuscript on one of those tools (GoMiner) has been cited in the literature almost 300 times. * Translationally significant results derived from a combination of 'integromic' molecular profiling studies and the bioinformatic developments. Five of those findings with clinical implications have been (i) biomarkers to distinguish colon from ovarian tumors of unknown origin, (ii) asparagine synthetase as a predictor of ovarian cancer cell response to L-asparaginase; (iii) the """"""""Permissive-Apoptosis Resistance"""""""" (PAR) two-step model for development of acquired drug resistance; (iv) 'MDR1-inverse' compounds more active in cancer cells that express MDR1; (v) critical evidence in the 1990's that led to clinical development of oxaliplatin, now a 'standard-of-care' agent for treatment of colon cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Intramural Research (Z01)
Project #
1Z01BC007349-16
Application #
7732915
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
16
Fiscal Year
2008
Total Cost
$336,151
Indirect Cost
Name
National Cancer Institute Division of Basic Sciences
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Liu, Hongfang; D'Andrade, Petula; Fulmer-Smentek, Stephanie et al. (2010) mRNA and microRNA expression profiles of the NCI-60 integrated with drug activities. Mol Cancer Ther 9:1080-91
Lorenzi, Philip L; Reinhold, William C; Varma, Sudhir et al. (2009) DNA fingerprinting of the NCI-60 cell line panel. Mol Cancer Ther 8:713-24
Okabe, Mitsunori; Szakacs, Gergely; Reimers, Mark A et al. (2008) Profiling SLCO and SLC22 genes in the NCI-60 cancer cell lines to identify drug uptake transporters. Mol Cancer Ther 7:3081-91
Sheehan, K M; Gulmann, C; Eichler, G S et al. (2008) Signal pathway profiling of epithelial and stromal compartments of colonic carcinoma reveals epithelial-mesenchymal transition. Oncogene 27:323-31
Ikediobi, Ogechi N; Reimers, Mark; Durinck, Steffen et al. (2008) In vitro differential sensitivity of melanomas to phenothiazines is based on the presence of codon 600 BRAF mutation. Mol Cancer Ther 7:1337-46
Martin, Scott E; Jones, Tamara L; Thomas, Cheryl L et al. (2007) Multiplexing siRNAs to compress RNAi-based screen size in human cells. Nucleic Acids Res 35:e57
Lee, Jae K; Havaleshko, Dmytro M; Cho, Hyungjun et al. (2007) A strategy for predicting the chemosensitivity of human cancers and its application to drug discovery. Proc Natl Acad Sci U S A 104:13086-91
Shankavaram, Uma T; Reinhold, William C; Nishizuka, Satoshi et al. (2007) Transcript and protein expression profiles of the NCI-60 cancer cell panel: an integromic microarray study. Mol Cancer Ther 6:820-32
Blower, Paul E; Verducci, Joseph S; Lin, Shili et al. (2007) MicroRNA expression profiles for the NCI-60 cancer cell panel. Mol Cancer Ther 6:1483-91
Kohn, Kurt W; Aladjem, Mirit I; Kim, Sohyoung et al. (2006) Depicting combinatorial complexity with the molecular interaction map notation. Mol Syst Biol 2:51

Showing the most recent 10 out of 37 publications