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Haopeng Xiao

Researcher at Harvard University

Publications -  38
Citations -  1704

Haopeng Xiao is an academic researcher from Harvard University. The author has contributed to research in topics: Proteomics & Glycoprotein. The author has an hindex of 17, co-authored 31 publications receiving 1035 citations. Previous affiliations of Haopeng Xiao include Georgia Institute of Technology.

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Efficacy, long-term toxicity, and mechanistic studies of gold nanorods photothermal therapy of cancer in xenograft mice.

TL;DR: The optimized properties of AuNRs and the conditions of PPTT to achieve maximal induction of tumor apoptosis and quantitative proteomics analysis in mouse tumor tissues suggest that the Au NRs-PPTT has potential as an approach to cancer therapy, and a long-term toxicity study shows that the platform is effective and safe for cancer therapy in mouse models.
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A Quantitative Tissue-Specific Landscape of Protein Redox Regulation during Aging

TL;DR: Oximouse is developed, a comprehensive and quantitative mapping of the mouse cysteine redox proteome in vivo that comprehensively identifies redox-modified disease networks that remodel in aged mice, establishing a systemic molecular basis for the long-standing proposed links between redox dysregulation and tissue aging.
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Targeting cancer cell integrins using gold nanorods in photothermal therapy inhibits migration through affecting cytoskeletal proteins

TL;DR: The ability of targeting AuNRs to cancer cell surface integrins and the introduction of NIR light to generate a mild plasmonic photothermal effect caused broad regulation on cytoskeletal proteins, thus impairing cancer cell migration and providing a potential medical application for controlling cancer metastasis.
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Simultaneous Time-Dependent Surface-Enhanced Raman Spectroscopy, Metabolomics, and Proteomics Reveal Cancer Cell Death Mechanisms Associated with Gold Nanorod Photothermal Therapy.

TL;DR: This study shows that the integration of the SERS with MS-based metabolomics and proteomics can assist the assignment of signals in SERS spectra and further characterize the related molecular mechanisms of the cellular processes involved in PPTT.