The Hematologic Malignancies Research Program at the University of New Mexico Cancer Center is a highly interactive transdisciplinary program with 25 Program Members from 4 Departments in the UNM School of Medicine (Medicine, Molecular Genetics and Microbiology, Pathology, and Pediatrics), 2 Departments on the UNM Main Campus (Mathematics, and Physics and Astronomy), and Los Alamos and Sandia National Laboratories. Research conducted by program members spans from the most basic interdisciplinary research, to translational investigations using human tissues and animal model systems, to the design of cancer clinical trials. The goals of the program are to: 1) use comprehensive genomic technologies and model systems to study the transcriptional regulation of hematopoiesis and the gene expression patterns of normal and leukemic cells in order to discover novel underlying genetic lesions in leukemia that may serve as new therapeutic targets;2) functionally characterize, image, and model signaling and adhesion pathways in normal and leukemic cells in order to understand how unique genetic abnormalities perturb these pathways to promote leukemogenesis and to identify targets for therapeutic intervention;and 3) translate program science and discoveries to novel diagnostic and therapeutic strategies and clinical trials at the UNM Cancer Center and within the NCI Cooperative Groups. Program members have used sophisticated genomic and computational technologies to develop gene expression classifiers for outcome prediction in leukemia and discover novel therapeutic targets in this disease (JAK2 mutations, CRLF2 activation, Metnase) that are being translated to clinical trials. These and other targets are also being studied in pre-clinical murine xenograft models to define the biochemical consequences of how these mutations perturb signaling pathways and to develop and test novel therapeutics. The development of advanced live cell imaging and spatiotemporal modeling technologies in the program are supporting high profile studies of receptors and signaling pathways involved in leukemogenesis. Since 2005, the program's funding and intra- and inter-programmatic interactions have significantly increased. Program members hold 3 interdisciplinary, multi-investigator, programmatic grants (one of 10 NIH National Centers for Systems Biology {P50GM085273;PI: Oliver);an LLS Specialized Center for Research in Leukemia {7388-06;PI: Willman);and a NCI Strategic Partnerships Grant {U01CA114762;PI: Willman)) and launched the first NCI TARGET Project to identify new therapeutic targets in high-risk pediatric ALL. Program members and their collaborators at St. Jude Children's Hospital and in the Children's Oncology Group have been notified of the awarding of a NCI ARRA TARGET Grant and a NCI ARRA Grand Opportunities Grant to continue to translate their work to leukemia clinical trials. As of September 2009, program members held $9,967,007 in total annual direct funding (representing a 44% increase in funding since 2005) of which $9,131,453 was peer-reviewed;annual direct NCI funding to the program has increased 55% to $2,448,182. In 2008, program members published a total of 64 cancer-relevant publications, of which 41 were intra-programmatic and 19% were inter-programmatic.
The Hematologic Malignancies Research Program integrates a team of transdisciplinary basic, translational, and clinical scientists who use highly sophisticated genomic, computational, imaging, and modeling approaches in human leukemia specimens and animal model systems to study how novel underlying genetic mutations in leukemia perturb gene expression and signaling and adhesion pathways to promote leukemogenesis. Discoveries are actively being translated to new diagnostic strategies and therapeutic modalities at the UNM Cancer Center and within the NCI Cooperative Oncology Groups.
| Peretti, Amanda S; Dominguez, Dayna; Grimes, Martha M et al. (2018) The R-Enantiomer of Ketorolac Delays Mammary Tumor Development in Mouse Mammary Tumor Virus-Polyoma Middle T Antigen (MMTV-PyMT) Mice. Am J Pathol 188:515-524 |
| Brandsma, Arianne M; Schwartz, Samantha L; Wester, Michael J et al. (2018) Mechanisms of inside-out signaling of the high-affinity IgG receptor Fc?RI. Sci Signal 11: |
| Zheng, Handong; Wu, Dandan; Wu, Xiang et al. (2018) Leptin Promotes Allergic Airway Inflammation through Targeting the Unfolded Protein Response Pathway. Sci Rep 8:8905 |
| Ray, Anita L; Berggren, Kiersten L; Restrepo Cruz, Sebastian et al. (2018) Inhibition of MK2 suppresses IL-1?, IL-6, and TNF-?-dependent colorectal cancer growth. Int J Cancer 142:1702-1711 |
| Hudson, Laurie G; Gillette, Jennifer M; Kang, Huining et al. (2018) Ovarian Tumor Microenvironment Signaling: Convergence on the Rac1 GTPase. Cancers (Basel) 10: |
| Licon-Munoz, Yamhilette; Fordyce, Colleen A; Hayek, Summer Raines et al. (2018) V-ATPase-dependent repression of androgen receptor in prostate cancer cells. Oncotarget 9:28921-28934 |
| Palsuledesai, Charuta C; Surviladze, Zurab; Waller, Anna et al. (2018) Activation of Rho Family GTPases by Small Molecules. ACS Chem Biol 13:1514-1524 |
| Sallmyr, Annahita; Tomkinson, Alan E (2018) Repair of DNA double-strand breaks by mammalian alternative end-joining pathways. J Biol Chem 293:10536-10546 |
| Kumar, Suresh; Jain, Ashish; Farzam, Farzin et al. (2018) Mechanism of Stx17 recruitment to autophagosomes via IRGM and mammalian Atg8 proteins. J Cell Biol 217:997-1013 |
| Vicuña, Belinda; Delaney, Harold D; Flores, Kristina G et al. (2018) Preferences for multigene panel testing for hereditary breast cancer risk among ethnically diverse BRCA-uninformative families. J Community Genet 9:81-92 |
Showing the most recent 10 out of 344 publications
