The DOI matches its Crossref record; 36 of the 36 references it cites were found in a registry or an index.
Protein typing of circulating microvesicles allows real-time monitoring of glioblastoma therapy
Open accessAbstract
Glioblastomas shed large quantities of small, membrane-bound microvesicles into the circulation. Although these hold promise as potential biomarkers of therapeutic response, their identification and quantification remain challenging. Here, we describe a highly sensitive and rapid analytical technique for profiling circulating microvesicles directly from blood samples of patients with glioblastoma. Microvesicles, introduced onto a dedicated microfluidic chip, are labeled with target-specific magnetic nanoparticles and detected by a miniaturized nuclear magnetic resonance system. Compared with current methods, this integrated system has a much higher detection sensitivity and can differentiate glioblastoma multiforme (GBM) microvesicles from nontumor host cell–derived microvesicles. We also show that circulating GBM microvesicles can be used to analyze primary tumor mutations and as a predictive metric of treatment-induced changes. This platform could provide both an early indicator of drug efficacy and a potential molecular stratifier for human clinical trials.
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Cites
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Self-citationIsolation and Characterization of Exosomes from Cell Culture Supernatants and Biological Fluids
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Self-citationCancer-associated IDH1 mutations produce 2-hydroxyglutarate
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Cited by
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“[121] report the fabrication of a microfluidic chip that quantifies the presence Nucleus Apoptosis Apoptotic bodies”
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Evidence-Based Clinical Use of Nanoscale Extracellular Vesicles in Nanomedicine
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Extracellular vesicles: A bright star of nanomedicine
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Metadata
- Authors
- Shao, H., Chung, J., Balaj, L., Charest, A., Bigner, D. D., Carter, B. S., Hochberg, F. H., Breakefield, X. O., Weissleder, R., & Lee, H.
- Venue
- Nature Medicine
- Published
- 2012-11-11
- Volume
- 18
- Issue
- 12
- Pages
- 1835-1840
- ISSN
- 1078-8956 (ISSN-L)
- 1546-170X
- OpenAlex
- W1987604193
- Cited by
- 759
- References
- 36
- FWCI
- 16.50
- Type
- journal article
- Language
- en
- Open access
- green
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- Shao, H., Chung, J., Balaj, L., Charest, A., Bigner, D. D., Carter, B. S., Hochberg, F. H., Breakefield, X. O., Weissleder, R., & Lee, H. (2012). Protein typing of circulating microvesicles allows real-time monitoring of glioblastoma therapy. Nature Medicine. https://doi.org/10.1038/nm.2994
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