Differentiation and function of transitional monocytes in cancer metastasis to the lung
Differentiation and function of transitional monocytes in cancer metastasis to the lung
批准号:
10748569
负责人:
Minhee (Emily) Park
金额:
$4.32万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2023
资助国家:
美国
项目状态:
未结题
起止时间:
2023-09-28 至 2025-12-31
关键词:
Activated Natural Killer CellAffectAlgorithmsAutomobile DrivingBone MarrowCSF1 geneCause of DeathCellsChimera organismComplementDataDendritic CellsDisseminated Malignant NeoplasmDistalEngineeringFamilyFloodsFlow CytometryFutureGoalsGrowthHematologic NeoplasmsHourImmuneImmune responseImmunityIn VitroInfiltrationInjectionsKnockout MiceLiteratureLungMacrophageMalignant NeoplasmsMediatingMelanoma CellMembrane ProteinsMetastatic Neoplasm to the LungModelingMolecularMusNatural Killer CellsNeoplasm Circulating CellsNeoplasm MetastasisOrganPathway interactionsPatientsPatternPhagocytesPhagocytosisPhasePhenotypePlayPrimary NeoplasmProcessReceptor SignalingReportingRoleSLAM proteinSignal InductionSignal PathwaySignal TransductionSiteSolidSurfaceSystemTechniquesTestingTimeTissuesTransgenic MiceUp-Regulationassaultcancer cellcell killingcell typeeffective therapyepigenomic profilingin vivoinsightmonocytemultiple omicsneoplastic cellnovel therapeutic interventionnovel therapeuticspermissivenesspreventprotein expressionproteomic signaturerecruitresidenceresponsetranscriptomic profilingtumortumor microenvironment
中文摘要
项目摘要/摘要
当癌细胞从起源地扩散到远端器官时,就会发生癌症转移,它是
实体癌患者的主要死因。当癌症扩散到肺部时,各种先天的
免疫细胞要么帮助,要么抑制这一殖民过程。单核细胞是最早的
转移开始时肺脏充血。这些单核细胞最终成为支持肿瘤的细胞
转移相关巨噬细胞(MAM),以及该领域的许多研究报告,单核细胞和
MAMs积极帮助转移性癌症渗入肺部并在那里定居。我的项目旨在
了解单核细胞如何分化为巨噬细胞集落刺激因子;尤其是,哪些信号和因素对此至关重要
过渡发生在肺部。此外,根据我的初步数据,我已经确定了一个时间窗口
哪些单核细胞已经发生了明显的表型变化,但尚未完全发育为巨噬细胞集落刺激因子。
有趣的是,这一过渡期也与其他免疫细胞类型的抗肿瘤活性相吻合,如
作为自然杀伤(NK)细胞。因此,我旨在研究促肿瘤单核细胞与抗肿瘤单核细胞之间的相互作用。
肿瘤中的NK细胞在肿瘤转移到肺部的头几个小时。通过理解如何将
这些相互作用的基础机制有助于增加肺转移建立的几率,即
将能够为预防转移的新的治疗努力贡献有价值的见解。
英文摘要
Project Summary/Abstract
Cancer metastasis occurs when cancer cells spread to distal organs from their site of origin, and it is the
leading cause of death in patients with solid cancers. When cancer spreads to the lung, various types of innate
immune cells either help or inhibit this colonization process. Monocytes are one of the earliest cell types to
flood the lung during the beginning of metastasis. These monocytes eventually become tumor-supporting
metastasis-associated macrophages (MAMs), and many studies in the field have reported that monocytes and
MAMs actively aid metastatic cancer to infiltrate the lung and take residence there. My project aims to
understand how monocytes differentiate into MAMs; in particular, what signals and factors are critical for this
transition to occur in the lung. Furthermore, from my preliminary data, I have identified a time window during
which monocytes have undergone clear phenotypic changes but have not yet fully developed into MAMs.
Interestingly, this transition period also coincides with the anti-tumor activity of other immune cell types, such
as natural killer (NK) cells. Therefore, I aim to study the interactions between pro-tumoral monocytes and anti-
tumoral NK cells during the first several hours of cancer metastasis to the lung. By understanding how the
mechanisms that underlie these interactions help to increase the odds of metastatic establishment in the lung, I
will be able to contribute valuable insights towards novel therapeutic efforts to prevent metastasis.
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