Bioinformatic Approaches for Understanding Macrophage Plasticity and Microbiome in Oral Diseases

项目来源

美国卫生和人类服务部基金(HHS)

项目主持人

FRIEDEN, LESLIE A

项目受资助机构

STATE UNIVERSITY OF NEW YORK AT BUFFALO

项目编号

1K18DE029526-01

立项年度

2020

立项时间

未公开

项目级别

国家级

研究期限

未知 / 未知

受资助金额

94393.00美元

学科

Aging; Dental/Oral and Craniofacial Disease; Genetics; Human Genome; Infectious Diseases; Microbiome;

学科代码

未公开

基金类别

Other Research Related

关键词

未公开

参与者

KIRKWOOD, KEITH L

参与机构

NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH

项目标书摘要:PROJECT SUMMARY Research: With advancing age, the immune system undergoes dynamic changes characterized by both impairment of adaptive immunity and activation of low-grade chronic inflammation. This chronic activation of inflammation associated with aging or `inflammaging'. Tristetraprolin (TTP) is an RNA binding protein that post- translationally binds to adenylate-uridylate?rich elements in the 3?-UTR of target mRNAs (including key pro- inflammatory mRNAs e.g. TNF?, COX-2 and IL-6) to promote their rapid turnover. Importantly, the project laboratory has demonstrated that failure to regulate expression of cytokines at the posttranscriptional level contributes to chronic inflammation and spontaneous alveolar bone loss with age in TTP-/- mice compared to age/sex match controls. Thus, TTP expression appears to be essential for alveolar bone homeostasis in an age- dependent manner. Data in this application and recently published data strongly support the concept that macrophages and myeloid-derived suppressor cell (MDSC) populations are expanded with age in TTP-/- mice, with concomitant reduction in lymphocyte populations. Taken together, these results support the notion that TTP may be a critical intrinsic factor of inflammaging and myeloid lineage expansion/differentiation that contributes towards skeletal homeostasis. For this K18 application, it is proposed to use data sets generated already under 5R01DE028258, to examine the role of the microbiome in contributing towards the TTP null hyperinflammatory phenotype and understand if MDSC populations from oral and non-oral sources have different expression profiles by single cell RNA sequencing. Fellowship training plan/environment: The applicant has assembled a strong mentoring team who have a long history of working together and training scientists to become successful independent investigators. The proposed project will allow the applicant to integrate his translation research portfolio with bioinformatics, which will foster the perspectives and skills necessary to continue to be a successful oral biologist.

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  • 1.The p38/MKP-1 signaling axis in oral cancer: Impact of tumor-associated macrophages

    • 关键词:
    • Oral cancer; MKP-1; Tumor microenvironment; p38 mitogen activatingkinases; Tumor-associated macrophages;SQUAMOUS-CELL CARCINOMA; ACTIVATED PROTEIN-KINASE; P38 MAPK; TGF-BETA;HUMAN HEAD; CETUXIMAB RESISTANCE; MOLECULAR-FEATURES; GENE-EXPRESSION;PPAR-GAMMA; INHIBITION

    Oral squamous cell carcinomas (OSCC) constitute over 95% of all head and neck malignancies. As a key component of the tumor microenvironment (TME), chronic inflammation contributes towards the development, progression, and regional metastasis of OSCC. Tumor associated macrophages (TAMs) associated with OSSC promote tumorigenesis through the production of cytokines and pro-inflammatory factors that are critical role in the various steps of malignant transformation, including tumor growth, survival, invasion, angiogenesis, and metastasis. The mitogen-activated protein kinases (MAPKs) can regulate inflammation along with a wide range of cellular processes including cell metabolism, proliferation, motility, apoptosis, survival, differentiation and play a crucial role in cell growth and survival in physiological and pathological processes including innate and adaptive immune responses. Dual specificity MAPK phosphatases (MKPs) deactivates MAPKs. MKPs are considered as an important feedback control mechanism that limits MAPK signaling and subsequent target gene expression. This review outlines the role of MKP-1, the founding member of the MKP family, in OSCC and the TME. Herein, we summarize recent progress in understanding the regulation of p38 MAPK/MKP-1 signaling pathways via TAM-related immune responses in OSCC development, progression and treatment outcomes.

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  • 2. Põldsalu, Inga; Rohtlaid, Kätlin; Plesse, Cedric; Vidal, Frédéric; Nguyen, Ngoc Tuan; Peikolainen, Anna-Liisa; Tamm, Tarmo; Kiefer, Rudolf (2020). Printed PEDOT:PSS Trilayer: Mechanism Evaluation and Application in Energy Storage. Materials, 13 (2), 491. DOI: 10.3390/ma13020491.

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