Integrated Training in Cancer Model Systems

项目来源

美国卫生和人类服务部基金(HHS)

项目主持人

DAMICO, MARK W

项目受资助机构

UNIV OF NORTH CAROLINA CHAPEL HILL

项目编号

5T32CA009156-45

立项年度

2020

立项时间

未公开

研究期限

未知 / 未知

项目级别

国家级

受资助金额

935418.00美元

学科

Cancer; Health Disparities; Minority Health;

学科代码

未公开

基金类别

TRAINING, INSTITUTIONAL

关键词

未公开

参与者

DER, CHANNING J.

参与机构

NATIONAL CANCER INSTITUTE

项目标书摘要:PROJECT SUMMARY This proposal seeks support for 14 postdoctoral fellows for a two year training curriculum within an established and highly successful program (Interdisciplinary Training in Cancer Model Systems ? ITCMS) that instills interdisciplinary approaches to address basic and translational approaches in cancer research. The 51 ITCMS mentors are chosen from 325 core faculty of the UNC Lineberger Cancer Center (LCCC). Faculty are housed within academic departments in the UNC School of Medicine, the College of Arts and Sciences, and the School of Pharmacy and are members of the five basic/translational LCCC programs: Cancer Cell Biology, Immunology, Molecular Therapeutics, Virology and Cancer Genetics as well as the Clinical Research Program. This pool of mentors allows fellows to engage in interdisciplinary studies from basic science to bioinformatics to translational studies, utilizing state of the art cancer models. The ITCMS program is administered by its Director and Associate Director, with advice from the Training Committee, and both External and Internal Advisory Boards. Preceptor and trainee input on the training program is accomplished through an annual, anonymous survey. Training is enhanced by access to the Center's core facilities, supported by the Center's NCI Core Grant (rated ?exceptional?). LCCC commitment to ITCMS is significant and includes support for an additional two postdoctoral slots. Fellows jointly apply to the ITCMS and one or more mentor laboratories and undergo a rigorous selection process. Upon appointment, each fellow develops a training plan approved by the mentor, the mentoring committee, and the Director. Each fellow participates in the following: (i) monthly in-house postdoctoral seminars given by the fellows, (ii) the annual Lineberger Postdoctoral-Faculty Research Day, organized by a Faculty Advisor and the Postdoctoral Fellows Committee, (iii) panel discussions on careers including advice for successful faculty applications and interviews, (iv) sessions on ethics in research (vi) a monthly research club, (vi) clinical exposure (physician shadowing and tumor board participation), (vii) interactions with patient advocates, and (viii) a grant writing and grant review program. Based on the individualized training plan, fellows participate in relevant training workshops (such as proteomics, microscopy, mouse histopathology, genomics, etc.). Progress is monitored annually by the Director and Associate Director, along with the Training Oversight Committee, before renewal for Year 2 support. Since its inception, the program has been committed to recruiting and successful training of minorities. The success of previous fellows, with the great majority continuing in a cancer or science-related field, underscores the importance placed on postdoctoral training in the ITCMS.

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  • 1.Activation and Evasion of Innate Immunity by Gammaherpesviruses

    • 关键词:
    • KSHV; EBV; MHV68; gammaherpesvirus; innate immunity;EPSTEIN-BARR-VIRUS; SARCOMA-ASSOCIATED-HERPESVIRUS; NF-KAPPA-B;TOLL-LIKE RECEPTORS; PLASMACYTOID DENDRITIC CELLS; NATURAL-KILLER-CELLS;SINGLE-STRANDED RNA; RIG-I; INTERFERON-ALPHA; CUTTING EDGE

    Gammaherpesviruses are ubiquitous pathogens that establish lifelong infections in the vast majority of adults worldwide. Importantly, these viruses are associated with numerous malignancies and are respon-sible for significant human cancer burden. These virus-associated cancers are due, in part, to the ability of gammaherpesviruses to successfully evade the innate immune response throughout the course of infec-tion. In this review, we will summarize the current understanding of how gammaherpesviruses are detected by innate immune sensors, how these viruses evade recognition by host cells, and how this knowledge can inform novel therapeutic approaches for these viruses and their associated diseases. (c) 2021 Elsevier Ltd. All rights reserved.

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  • 2.Stress Relief Techniques: p38 MAPK Determines the Balance of Cell Cycle and Apoptosis Pathways

    • 关键词:
    • cell cycle; cell signaling; apoptosis; mitosis; chemotherapy; kinase;protein networks; DNA damage; cell stress;ACTIVATED PROTEIN-KINASE; OUTER-MEMBRANE PERMEABILIZATION; N-TERMINALPHOSPHORYLATION; DNA-DAMAGE; BCL-2 FAMILY; RETINOBLASTOMA PROTEIN;UP-REGULATION; P38-ALPHA MAPK; CDK INHIBITORS; BH3 DOMAINS

    Protein signaling networks are formed from diverse and inter-connected cell signaling pathways converging into webs of function and regulation. These signaling pathways both receive and conduct molecular messages, often by a series of post-translation modifications such as phosphorylation or through protein-protein interactions via intrinsic motifs. The mitogen activated protein kinases (MAPKs) are components of kinase cascades that transmit signals through phosphorylation. There are several MAPK subfamilies, and one subfamily is the stress-activated protein kinases, which in mammals is the p38 family. The p38 enzymes mediate a variety of cellular outcomes including DNA repair, cell survival/cell fate decisions, and cell cycle arrest. The cell cycle is itself a signaling system that precisely controls DNA replication, chromosome segregation, and cellular division. Another indispensable cell function influenced by the p38 stress response is programmed cell death (apoptosis). As the regulators of cell survival, the BCL2 family of proteins and their dynamics are exquisitely sensitive to cell stress. The BCL2 family forms a protein-protein interaction network divided into anti-apoptotic and pro-apoptotic members, and the balance of binding between these two sides determines cell survival. Here, we discuss the intersections among the p38 MAPK, cell cycle, and apoptosis signaling pathways.

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  • 3.Binge Drinking: Macropinocytosis Promotes Tumorigenic Growth of RAS-Mutant Cancers

    • 关键词:
    • PROTEIN

    The RAS oncoprotein drives elevated macropinocytosis, a metabolic process essential for cancer growth. A recent study by Ramirez et al. elucidated a mechanism whereby RAS controls V-ATPase association-with the plasma membrane to drive RAC1 GTPase-dependent macropinocytosis. Potentially actionable targets to disrupt this RAS-dependent nutrient acquisition pathway were identified.

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  • 4.Mitochondrial GSDMD Pores DAMPen Pyroptosis

    • 关键词:
    • UPSTREAM

    Noncanoncial inflammasome activation by cytosolic lipopolysaccharide (LPS) causes pyroptotic cell death facilitated by gasdermin D (GSDMD) pore formation. In this issue of Immunity, Huang et al. describe how cytosolic LPS in endothelial cells does not cause cell death but restrains endothelial cell proliferation.

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