? IMMUNOLOGY, MICROENVIRONMENT AND METASTASIS The Immunology, Microenvironment and Metastasis (IMM) Program was launched in 2017 to respond to two strategic needs in the Cancer Center: (i) create an interdisciplinary but cohesive hub for basic and translational tumor immunology research; and (ii) expand a bench-to-bedside effort focused on the tumor microenvironment as a fundamental disease driver and prime therapeutic target. The resulting IMM Program originated from the merge of the former Tumor Microenvironment and Metastasis (TMM) Program in the Cancer Center with the Translational Tumor Immunology (TTI) initiative launched at the Institute in 2015. The ten Cancer Center members that currently comprise the IMM Program have experimental interests that closely align with three main research themes in the biology of the tumor microenvironment: (i) mechanisms of local immunosuppression; (ii) tumor-host crosstalk in disease progression and treatment response; and (iii) pathways of metastatic competence. Despite its relatively recent launch, the IMM Program has critically contributed to all overarching priorities of the Cancer Center, leading successful faculty recruitment in tumor immunology and metastasis, spearheading extensive intra- and inter-programmatic collaborations, promoting broad utilization of Cancer Center Shared Resources, and moving research discoveries to the clinic through successful inter-institutional partnerships. Published in the top-tier literature, contributions from IMM Program members uncovered novel circuitries of immunosuppression by Myeloid-Derived Suppressor Cells (MDSC), characterized new signals of how changes in an aging microenvironment dictate melanoma progression, and defined the contribution of stress-induced mitochondrial reprogramming in metastasis. As a result, the IMM Program currently receives $3 million in NCI funding and a total, cancer-related funding base of $4.7 million, has a rate of collaborative publications of over 40% (intra- and inter-programmatic combined), and 66% of its peer-reviewed, cancer-related funding ($2.3 million) is the product of internal or external collaborations. Currently, the IMM Program contributes to one Specialized Program of Research Excellence (SPORE) in melanoma, three Program Project grants, four multi-PI awards and one U01 grant. Building on these scientific accomplishments, an enveloping culture of transdisciplinary collaboration, and firm commitment to bench-to- bedside cancer research, the IMM Program is ideally poised to fulfill the strategic objectives of the Cancer Center during the next CCSG budget cycle. These will include strengthening an Institute-wide effort in basic and translational immunology synergistically with a reorganized Wistar Vaccine and Immunotherapy Center, expand inter-programmatic contributions in the melanoma research continuum signature, define the interplay between stromal and tumor cells in the emergence of aggressive disease traits, and elucidate mechanisms of metastasis as actionable therapeutic targets.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA010815-52
Application #
10145622
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
1997-04-01
Project End
2024-02-29
Budget Start
2021-03-01
Budget End
2022-02-28
Support Year
52
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Wistar Institute
Department
Type
DUNS #
075524595
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Hu, Xiaowen; Sood, Anil K; Dang, Chi V et al. (2018) The role of long noncoding RNAs in cancer: the dark matter matters. Curr Opin Genet Dev 48:8-15
Liu, Shujing; Zhang, Gao; Guo, Jianping et al. (2018) Loss of Phd2 cooperates with BRAFV600E to drive melanomagenesis. Nat Commun 9:5426
Saglam, Ozlen; Conejo-Garcia, Jose (2018) PD-1/PD-L1 immune checkpoint inhibitors in advanced cervical cancer. Integr Cancer Sci Ther 5:
Papasavvas, Emmanouil; Lada, Steven M; Joseph, Jocelin et al. (2018) Analytical ART interruption does not irreversibly change pre-interruption levels of cellular HIV. AIDS :
Duperret, Elizabeth K; Trautz, Aspen; Stoltz, Regina et al. (2018) Synthetic DNA-Encoded Monoclonal Antibody Delivery of Anti-CTLA-4 Antibodies Induces Tumor Shrinkage In Vivo. Cancer Res 78:6363-6370
Kugel 3rd, Curtis H; Douglass, Stephen M; Webster, Marie R et al. (2018) Age Correlates with Response to Anti-PD1, Reflecting Age-Related Differences in Intratumoral Effector and Regulatory T-Cell Populations. Clin Cancer Res 24:5347-5356
Reyes-Uribe, Patricia; Adrianzen-Ruesta, Maria Paz; Deng, Zhong et al. (2018) Exploiting TERT dependency as a therapeutic strategy for NRAS-mutant melanoma. Oncogene 37:4058-4072
Bhattacharjee, Souvik; Coppens, Isabelle; Mbengue, Alassane et al. (2018) Remodeling of the malaria parasite and host human red cell by vesicle amplification that induces artemisinin resistance. Blood 131:1234-1247
Fukumoto, Takeshi; Park, Pyoung Hwa; Wu, Shuai et al. (2018) Repurposing Pan-HDAC Inhibitors for ARID1A-Mutated Ovarian Cancer. Cell Rep 22:3393-3400
Thangavel, Chellappagounder; Boopathi, Ettickan; Liu, Yi et al. (2018) Therapeutic Challenge with a CDK 4/6 Inhibitor Induces an RB-Dependent SMAC-Mediated Apoptotic Response in Non-Small Cell Lung Cancer. Clin Cancer Res 24:1402-1414

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