Paclitaxel is incorporated by mesenchymal stromal cells and released in exosomes that inhibit in vitro tumor growth: a new approach for drug delivery.
By L. Pascucci, V. Coccè, A. Bonomi, Diletta Ami, P. Ceccarelli, E. Ciusani, L. Viganò, A. Locatelli, F. Sisto, S. Doglia and 6 more. Journal of Controlled Release, 2014
818 citations recorded by the source corpus.
Subfields: Cancer Research, Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/95f6b21a9997b53301c9dd770c02fb4d939c105b
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Citations in the corpus
- Development of Exosome-encapsulated Paclitaxel to Overcome MDR in Cancer cells (2015, neutral): “The same effect was reported with PTX in Pgp-overexpressing bone marrow mesenchymal stromal cells (SR4987) (45).”
- Applying extracellular vesicles based therapeutics in clinical trials – an ISEV position paper (2015, background): “PTX-loaded EVs, released from PTX-treated MSCs in vitro, have been shown to inhibit the proliferation of cultured tumour cells (240).”
- Exosome: A Review of Its Classification, Isolation Techniques, Storage, Diagnostic and Targeted Therapy Applications (2020, neutral): “23 In addition, MSC exosomes have been shown to play a role in the development of many diseases.”
- Exosome Theranostics: Biology and Translational Medicine (2018, background): “In addition, other therapeutic compounds, such as paclitaxel [172] and doxorubicin [173], can be packaged into exosomes for crossing the blood-brain barrier and achieving targeted delivery.”