2021
DOI: 10.1167/iovs.62.14.13
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Carboplatin- and Etoposide-Loaded Lactoferrin Protein Nanoparticles for Targeting Cancer Stem Cells in Retinoblastoma In Vitro

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Cited by 34 publications
(18 citation statements)
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“…40 Lactoferrin nanoparticles (Lf-Nps) have been evaluate for cytotoxicity of etoposide, (topoisomerase inhibitor) and carboplatin in vitro, against the growth of retinoblastoma-Y79 cells. 41 Lactoferrin is an iron transporting glycoprotein (transferrin family) shown to improve target recognition in several studies. 42 The drug localization observed with lactoferrin nanoparticles is associated with expression of lactoferrin receptors in target cancer cells.…”
Section: Effective Treatment Approachmentioning
confidence: 99%
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“…40 Lactoferrin nanoparticles (Lf-Nps) have been evaluate for cytotoxicity of etoposide, (topoisomerase inhibitor) and carboplatin in vitro, against the growth of retinoblastoma-Y79 cells. 41 Lactoferrin is an iron transporting glycoprotein (transferrin family) shown to improve target recognition in several studies. 42 The drug localization observed with lactoferrin nanoparticles is associated with expression of lactoferrin receptors in target cancer cells.…”
Section: Effective Treatment Approachmentioning
confidence: 99%
“…42 Narayana et al, confirmed significant intracellular drug uptake, and cytotoxicity profile, for carboplatin (CPT)-and etoposide (ETP)-loaded lactoferrin nanoparticles (Lf-Nps) in retinoblastoma Y79 cells. 41 Drug agents loaded in lactoferrin nanoparticles (Lf-Nps) doubled overall cellular uptake compared to carboplatin (CPT) or etoposide (ETP) alone. 41 Additionally, the cytotoxic effect increased up to 50% with carboplatin (CPT)-and etoposide (ETP)loaded lactoferrin nanoparticles(Lf-Nps) compared to controls.…”
Section: Effective Treatment Approachmentioning
confidence: 99%
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“…[ 5 6 ] In our attempt to investigate the role of CSCs in Y79 cell line, we had demonstrated that FSC lo /SSC lo /CD133 lo subset has the properties of CSCs in vitro such as colony-forming ability, differentiation, chemoresistance, invasion, and stem cell-specific gene expression signature. [ 7 8 ] Translation of in vitro studies to in vivo model systems has become an integral part of functional tumor biology studies and clinically relevant model systems help in developing better treatment strategies. [ 9 ] Several genetic and xenograft animal models have been established to explore Rb tumorigenesis, metastasis, and targeted therapies.…”
mentioning
confidence: 99%