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[MONC Membership Roster] [MONC Meeting Rosters]
The Molecular Oncogenesis [MONC] Study Section reviews applications that focus on the early molecular events that lead to immortalization and oncogenic transformation such as the identification of oncogenes and tumor suppressor genes, alterations in signaling, growth, and cell cycle control pathways, and protein stability/degradation mechanisms. Applications dealing with normal developmental processes as they pertain to oncogenic transformation, including the identification and characterization of progenitor and cancer stem cells are also considered. Specific areas covered by MONC:
- Identification of oncogenes and tumor suppressor genes or alterations in their expression, regulation or function that may contribute to oncogenic transformation
- Alterations in signal transduction pathways that may modulate or lead to oncogenic transformation
- Identification and characterization of progenitor cells and cancer stem cells that may be involved in oncogenic transformation
- Cell cycle regulation and dysregulation that may contribute to early oncogenic transformation
- Proteasome-mediated degradation: Mechanisms and/or alterations of protein stability that could contribute to transformation, including post-translation modification such as ubiquitylation or sumoylation
The study sections with the most closely related of similar science listed in rank order are:
Cancer Molecular Pathobiology Study Section [CAMP] Tumor Cell Biology Study Section [TCB] Cancer Etiology Study Section [CE] Cancer Genetics Study Section [CG] Cellular Signaling and Regulatory Systems Study Section [CSRS]
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[TCB Membership Roster] [TCB Meeting Rosters]
The Tumor Cell Biology [TCB] Study Section reviews applications concerned with signal transduction mechanisms in neoplastic cells, regulation of tumor cell phenotype and behavior, and tumor progression. Emphasis is on signaling processes mediated by kinases, phospahatases and other molecules, including oncogenes, tumor suppressors, various growth factors and receptors, in tumor cells and animal tumor models. Specific areas covered by TCB:
- Signal transduction processes mediated by kinases and phosphatases and other molecules, including growth factors, nuclear factors and receptors
- Pathways regulated by oncogenes and tumor suppressors that affect tumor cell phenotype and behavior, such as survival, proliferation, and death
- The analysis of the composition and function of signaling complexes and their interactions among different signaling pathways in the context of tumor biology and tumor progression
- Hormonal modulation of tumorigenesis, including endocrine signaling and hormone receptors mechanisms
- Mechanisms that regulate differentiation and trans-differentiation in neoplasia, signal transduction mediated by cytoskeletal components and nutrient sensing mechanisms in tumor biology
The study sections with most closely related areas of similar science listed in rank order are:
Cancer Molecular Pathobiology [CAMP] Tumor Progression and Metastasis [TPM] Tumor Microenvironment [TME] Molecular Oncogenesis [MONC] Cancer Etiology [CE]
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[TME Membership Roster] [TME Meeting Rosters]
The Tumor Microenvironment [TME] Study Section reviews grant applications that deal with basic mechanisms of interactions between tumor and host system including stroma cells, extracellular matrix (ECM) and extracellular molecules. Emphasis is on evaluation of the tumor as an organ-like structure with complex, dynamic cross-talk. Studies of tumor-stroma interactions including cell-cell interaction, tumor induced alterations of ECM during tumor progression and metastasis, tumor angiogenesis and lymphangiogenesis, and organ specific metastasis are assigned to this study section. Specific areas covered by TME:
- Molecular and cellular aspects of bi-directional interaction between tumor and stromal cells (including fibroblasts, glial cells, epithelial cells, adipocytes, immune cells, inflammatory cells, vascular compartments, and bone marrow cells) during neoplastic progression, tumor angiogenesis, growth and metastasis, including studies of cancer stem cell niche and tumor cell dormancy
- Evaluation of tumor induced alterations in extracellular matrix during tumor progression. Cellular and molecular aspects of epithelial-mesenchymal transition (EMT) and transactivation as it relates to tumor progression
- Dynamics of cell-cell communication for tumor cell survival, growth and invasion focusing on cell adhesion molecules, cell junctions, as well as intercellular signaling and production of paracrine factors, chemokines, and inflammatory cytokines
- Development and exploration and physiologically responsive in vitro 3D matrix and organotypic models and animal models that allow investigation of tumor cells in the context of a tissue-like and in vivo environment
- Development and investigation of models for studying organ-specific metastases, crucial interactions between metastatic cells and site specific organs including bone/bone marrow microenvironment and other site-specific organs such as lung and brain
The study sections with most closely related areas of similar science listed in rank order are:
Tumor Progression and Metastasis Study Section [TPM] Tumor Cell Biology Study Section [TCB] Transplantation, Tolerance and Tumor Immunology Study Section [TTT] Hematopoiesis Study Section [HP] Cellular Mechanisms in Aging and Development Study Section [CMAD]
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[TPM Membership Roster] [TPM Meeting Rosters]
The Tumor Progression and Metastasis [TPM] Study Section reviews grant applications that deal with the basic mechanisms of cancer progression, metastasis, invasion/migration and angiogenesis. Special emphasis is placed on hypoxia, inflammation, tumor imaging and pathology, adhesion, and growth. Studies focusing on cytoskeleton, proteases, wound healing, extracellular matrix remodeling, suppressors/inhibitors of metastasis & angiogenesis, and animal models of metastasis & angiogenesis will also be assigned to this study section. Specific areas covered by TPM:
- Transcriptional, posttranscriptional, translational and posttranslational regulation of tumor metastasis and angiogenesis including role of microRNA (miRNA), small inhibitory RNA (siRNA), short hairpin RNA (shRNA), small activating RNA (saRNA), ubiquitination, acetylation, and phosphorylation
- Tumor cell adhesion, invasion/migration, and angiogenesis including angiogenic factors and their receptors.
- Role of stress in tumor metastasis & angiogenesis including the function of hypoxia and inflammation
- In vitro and in vivo models of tumor metastasis and angiogenesis including genetics and imaging analysis
- Contribution of carbohydrate modifications, wound healing, and cell membrane specializations (e.g., caveolae and lipid rafts) as they relate to tumor invasion
- Role of stem cells in tumor metastasis and angiogenesis
The study sections with most closely related areas of similar science listed in rank order are:
Tumor Microenvironment Study Section [TME] Tumor Cell Biology Study Section [TCB] Cancer Molecular Pathobiology Study Section [CAMP] Basic Mechanisms of Cancer Therapeutics Study Section [BMCT] Intercellular Interactions Study Section [ICI]
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