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The Potential of Nanoparticle-Mediated Macrophage Polarization for Solid Tumor Therapy : = Evidence Synthesis and Temporal Monitoring.

紀錄類型:	書目-語言資料,手稿 : Monograph/item
正題名/作者:	The Potential of Nanoparticle-Mediated Macrophage Polarization for Solid Tumor Therapy :/
其他題名:	Evidence Synthesis and Temporal Monitoring.
作者:	Bilynsky, Colette Sandra Macedo.
面頁冊數:	1 online resource (215 pages)
附註:	Source: Dissertations Abstracts International, Volume: 85-10, Section: B.
Contained By:	Dissertations Abstracts International85-10B.
標題:	Biomedical engineering. -
電子資源:	click for full text (PQDT)
ISBN:	9798382310176

The Potential of Nanoparticle-Mediated Macrophage Polarization for Solid Tumor Therapy : = Evidence Synthesis and Temporal Monitoring.
Bilynsky, Colette Sandra Macedo.

The Potential of Nanoparticle-Mediated Macrophage Polarization for Solid Tumor Therapy :Evidence Synthesis and Temporal Monitoring. - 1 online resource (215 pages)

Source: Dissertations Abstracts International, Volume: 85-10, Section: B.

Thesis (Ph.D.)--Carnegie Mellon University, 2024.

Includes bibliographical references

Cancer persists as a significant public health challenge despite treatment advances. Colorectal cancer is especially a concern because its incidence and mortality are increasing in young individuals. Solid tumors, such as colorectal cancer, are challenging to treat with immunotherapies due to their immunosuppressive microenvironment preventing T cell infiltration. Tumor-associated macrophages (TAMs) play a pivotal role in supporting this immunosuppression by adopting an anti-inflammatory and pro-tumoral phenotype within the tumor microenvironment. Leveraging nanoparticles to repolarize TAMs towards a proinflammatory and tumoricidal phenotype holds promise for solid tumor therapy. However, clinical translation of cancer nanomedicines has been slow. This dissertation aims to address this through quantitative review of the intersection between the colorectal cancer nanomedicine and macrophage polarization, and by proposing a novel method of temporally tracking macrophage polarization using bioluminescent reporter cells.Using eLDA topic modeling, the dissertation identifies six major topics in the intersection of cancer medicine and macrophage polarization, providing insights into nanoparticle design choices and therapeutic strategies across various cancer types. A scoping review and meta-analysis of colorectal cancer nanomedicine over two decades reveal evolving nanoparticle design strategies and their impact on macrophage polarization. We also demonstrate how a nanoparticle's ability to increase macrophages' ratio of M1 to M2 polarization is correlated with their efficacy at reducing tumor growth and increasing survival. This dissertation also includes a technology assessment of how evidence synthesis of preclinical studies informs open science policy.To better temporally track macrophage polarization, the dissertation introduces a method utilizing THP-1 reporter cells with bioluminescently labeled polarization-relevant transcription factors. We demonstrated how these reporter cells enable time-resolved activation curves for tumor-associated macrophages, revealing unique NFκB activation profiles dependent on cancer type that we linked to the tumor microenvironments immunogenicity. Furthermore, monitoring monocyte to macrophage differentiation with this method highlights the importance of selecting appropriate differentiation protocols for the intended use. These examples demonstrate the potential use of this bioluminescent platform to monitor macrophage polarization in response to immunomodulatory treatments, like macrophage-targeted cancer nanomedicine.

Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2024

Mode of access: World Wide Web

ISBN: 9798382310176Subjects--Topical Terms:

588770
Biomedical engineering.
Subjects--Index Terms:

Colorectal cancerIndex Terms--Genre/Form:

554714
Electronic books.

The Potential of Nanoparticle-Mediated Macrophage Polarization for Solid Tumor Therapy : = Evidence Synthesis and Temporal Monitoring.
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