? HEMATOLOGIC MALIGNANCIES AND CELLULAR THERAPIES PROGRAM The Hematologic Malignancies and Cellular Therapies Program (HMCT) is a multidisciplinary clinical, basic and translational research effort whose theme is to facilitate research with the ultimate objective to improve outcomes for patients with hematological malignancies. The broad, long-term goals of HMCT are to build on and extend current knowledge in the field of hematopoietic stem cell transplantation, immunotherapy and hematological malignancies, and to develop novel strategies for improving therapeutic results in patients with hematological malignancies through a collaborative and integrated approach involving the basic, translational and clinical investigators of HMCT. The HMCT has two focus areas related to our scientific aims and theme: 1) Understanding the interplay between hematopoietic/immune cells and their microenvironment with respect to immune activation and suppression; and 2) translating laboratory-based observations to clinical trials. Among the strengths of the program are the significant numbers of physician scientists working on fundamental problems in hematological malignancies and who are able to take the basic observations at the bench to the bedside through extensive collaborations with the clinical researchers. Specially, the scientific goals of the HMCT Program are: 1) To understand the role of the external environment and microenvironment in immune responses; 2) To elucidate the role of immune and stromal cells in anti-tumor responses and graft-vs.-host disease (GVHD); 3) To develop and execute investigator-initiated translational trials for hematologic malignancies - all with the goal to stimulate and facilitate intra- and inter-programmatic collaborations; 4) To further advance genomic signatures in hematological malignancies and evaluate the role of different signaling mechanisms and; 5) To train the next generation of MD, PhD, and M.D./Ph.D. students, postdoctoral, fellows, residents in the field of adult and pediatric hematopoietic stem cell transplantation, immunotherapy and hematological malignancies. The Program includes 36 primary and 9 secondary members from 6 departments and two schools within Duke University. Total direct funding for program members is $17.2M, of which $4.4M is peer-reviewed, including $1.6M from the NCI. From 2014- 2018, program members published 457 papers in peer-reviewed journals, 21% were intra-programmatic and 28% were inter-programmatic collaborations. During the current grant period, the program enrolled 1,519 subjects to all trials, 923 to interventional trials, and 587 to treatment trials.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA014236-46
Application #
9853603
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2020-01-01
Budget End
2020-12-31
Support Year
46
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Duke University
Department
Type
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Káradóttir, Ragnhildur T; Kuo, Chay T (2018) Neuronal Activity-Dependent Control of Postnatal Neurogenesis and Gliogenesis. Annu Rev Neurosci 41:139-161
Han, Peng; Liu, Hongliang; Shi, Qiong et al. (2018) Associations between expression levels of nucleotide excision repair proteins in lymphoblastoid cells and risk of squamous cell carcinoma of the head and neck. Mol Carcinog 57:784-793
Xu, Yinghui; Wang, Yanru; Liu, Hongliang et al. (2018) Genetic variants in the metzincin metallopeptidase family genes predict melanoma survival. Mol Carcinog 57:22-31
Abdi, Khadar; Kuo, Chay T (2018) Laminating the mammalian cortex during development: cell polarity protein function and Hippo signaling. Genes Dev 32:740-741
Lu, Min; Sanderson, Sydney M; Zessin, Amelia et al. (2018) Exercise inhibits tumor growth and central carbon metabolism in patient-derived xenograft models of colorectal cancer. Cancer Metab 6:14
Qian, Danwen; Liu, Hongliang; Wang, Xiaomeng et al. (2018) Potentially functional genetic variants in the complement-related immunity gene-set are associated with non-small cell lung cancer survival. Int J Cancer :
Ashcraft, Kathleen A; Choudhury, Kingshuk Roy; Birer, Sam R et al. (2018) Application of a Novel Murine Ear Vein Model to Evaluate the Effects of a Vascular Radioprotectant on Radiation-Induced Vascular Permeability and Leukocyte Adhesion. Radiat Res 190:12-21
Ong, Cecilia T; Campbell, Brittany M; Thomas, Samantha M et al. (2018) Metaplastic Breast Cancer Treatment and Outcomes in 2500 Patients: A Retrospective Analysis of a National Oncology Database. Ann Surg Oncol 25:2249-2260
Duan, Bensong; Hu, Jiangfeng; Liu, Hongliang et al. (2018) Genetic variants in the platelet-derived growth factor subunit B gene associated with pancreatic cancer risk. Int J Cancer 142:1322-1331
Wu, Mengxi; Huang, Po-Hsun; Zhang, Rui et al. (2018) Circulating Tumor Cell Phenotyping via High-Throughput Acoustic Separation. Small 14:e1801131

Showing the most recent 10 out of 513 publications