? HEMATOLOGIC MALIGNANCIES The Hematologic Malignancies (HM) Program of the Lurie Cancer Center (LCC) combines the talents and expertise of outstanding basic scientists, nationally recognized clinical researchers, and translational investigators. The goal of the program is to leverage discoveries from member laboratories into clinical interventions for the treatment of malignant hematologic diseases. This goal is pursued through two program aims: a) Identify key pathways that regulate hematopoiesis and lymphopoiesis and determine the functional significance of their alteration in hematologic malignancies, and b) Define molecular therapeutic targets and evaluate the efficacy of novel agents in clinical trials for hematologic malignancies. Disease specific areas of focus for program members include acute and chronic myeloid leukemia, myeloproliferative neoplasms (MPNs), acute and chronic lymphoid leukemia, lymphomas, and multiple myeloma. HM members have made significant contributions to our understanding of molecular and cellular drivers of hematologic malignancies; specifically, in the areas of epigenetic modification, cellular signaling and gene expression. Translation of these results to clinical trials is facilitated by an extensive network of collaborative interactions between laboratory-based faculty and clinical investigators in the program. During the current funding period, such intra-programmatic interactions resulted in a number of therapeutic clinical trials that were developed from work in investigator laboratories. This multidisciplinary inter-departmental program has 32 members from 10 departments in 3 schools. During the current funding period, program members published 520 papers that were relevant to malignant hematologic diseases. 131 (25%) of these publications represented intra-programmatic collaborations, 91 (18%) inter- programmatic collaborations, and 68% involved inter-institutional collaborations. 143 (28%) were high impact (impact factor >9). Peer reviewed funding for program members totaled $5,190,595 (direct) with $2,117,851 (direct) from the NCI, and $3,072,744 (direct) from other NIH institutes and other sources. Program Leader Elizabeth Eklund, MD and co-leader Leo Gordon, MD have complementary expertise in the areas of laboratory investigation, translational research and clinical trials for hematologic malignancies. They work together to foster collaborative interactions between program members through regularly occurring clinical and research oriented conferences, retreats and other program activities.!

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA060553-26
Application #
9982878
Study Section
Special Emphasis Panel (ZCA1)
Project Start
Project End
Budget Start
2020-08-01
Budget End
2021-07-31
Support Year
26
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Northwestern University at Chicago
Department
Type
DUNS #
005436803
City
Chicago
State
IL
Country
United States
Zip Code
60611
Kaplan, Nihal; Ventrella, Rosa; Peng, Han et al. (2018) EphA2/Ephrin-A1 Mediate Corneal Epithelial Cell Compartmentalization via ADAM10 Regulation of EGFR Signaling. Invest Ophthalmol Vis Sci 59:393-406
Kenig-Kozlovsky, Yael; Scott, Rizaldy P; Onay, Tuncer et al. (2018) Ascending Vasa Recta Are Angiopoietin/Tie2-Dependent Lymphatic-Like Vessels. J Am Soc Nephrol 29:1097-1107
Zhang, Angelica; Veesenmeyer, Jeffrey L; Hauser, Alan R (2018) Phosphatidylinositol 4,5-Bisphosphate-Dependent Oligomerization of the Pseudomonas aeruginosa Cytotoxin ExoU. Infect Immun 86:
Ting, See-Yeun; Bosch, Dustin E; Mangiameli, Sarah M et al. (2018) Bifunctional Immunity Proteins Protect Bacteria against FtsZ-Targeting ADP-Ribosylating Toxins. Cell 175:1380-1392.e14
Nahum-Shani, Inbal; Smith, Shawna N; Spring, Bonnie J et al. (2018) Just-in-Time Adaptive Interventions (JITAIs) in Mobile Health: Key Components and Design Principles for Ongoing Health Behavior Support. Ann Behav Med 52:446-462
Kang, Hong-Jun; Song, Ha Yong; Ahmed, Mohamed A et al. (2018) NQO1 regulates mitotic progression and response to mitotic stress through modulating SIRT2 activity. Free Radic Biol Med 126:358-371
Long, Alan; Dominguez, Donye; Qin, Lei et al. (2018) Type 2 Innate Lymphoid Cells Impede IL-33-Mediated Tumor Suppression. J Immunol 201:3456-3464
Lewis, Phillip L; Su, Jimmy; Yan, Ming et al. (2018) Complex bile duct network formation within liver decellularized extracellular matrix hydrogels. Sci Rep 8:12220
Hong, Bong Jin; Iscen, Aysenur; Chipre, Anthony J et al. (2018) Highly Stable, Ultrasmall Polymer-Grafted Nanobins (usPGNs) with Stimuli-Responsive Capability. J Phys Chem Lett 9:1133-1139
Smith, Erica D; Garza-Gongora, Arturo G; MacQuarrie, Kyle L et al. (2018) Interstitial telomeric loops and implications of the interaction between TRF2 and lamin A/C. Differentiation 102:19-26

Showing the most recent 10 out of 1972 publications