Folate Receptor-Targeted Polymeric Micellar Nanocarriers for Delivery of Orlistat as a Repurposed Drug against Triple-Negative Breast Cancer (Q36563827)

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scientific article published on 9 November 2015

Language	Label	Description	Also known as
English	Folate Receptor-Targeted Polymeric Micellar Nanocarriers for Delivery of Orlistat as a Repurposed Drug against Triple-Negative Breast Cancer	scientific article published on 9 November 2015

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scholarly article

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29 February 2020

Folate Receptor-Targeted Polymeric Micellar Nanocarriers for Delivery of Orlistat as a Repurposed Drug against Triple-Negative Breast Cancer (English)

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29 February 2020

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Rohith Bhethanabotla

2

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Rammohan Devulapally

4

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author name string

Ramasamy Paulmurugan

1

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Kaushik Mishra

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Kira Foygel

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Thillai V Sekar

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Jeyarama S Ananta

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Tarik F Massoud

8

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Abraham Joy

9

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publication date

9 November 2015

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Molecular Cancer Therapeutics

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15

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221-231

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2

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29 February 2020

describes a project that uses

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Formulation of Anti-miR-21 and 4-Hydroxytamoxifen Co-loaded Biodegradable Polymer Nanoparticles and Their Antiproliferative Effect on Breast Cancer Cells.

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Ultrasound-guided delivery of microRNA loaded nanoparticles into cancer

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Polymer nanoparticles mediated codelivery of antimiR-10b and antimiR-21 for achieving triple negative breast cancer therapy.

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Metformin-induced killing of triple-negative breast cancer cells is mediated by reduction in fatty acid synthase via miRNA-193b

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Folate receptor alpha (FRA) expression in breast cancer: identification of a new molecular subtype and association with triple negative disease

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Integrated microRNA and mRNA signatures associated with survival in triple negative breast cancer

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Targeting energy metabolic and oncogenic signaling pathways in triple-negative breast cancer by a novel adenosine monophosphate-activated protein kinase (AMPK) activator

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Knockdown of miR-21 in human breast cancer cell lines inhibits proliferation, in vitro migration and in vivo tumor growth

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Obesity management: update on orlistat.

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Antitumoral actions of the anti-obesity drug orlistat (XenicalTM) in breast cancer cells: blockade of cell cycle progression, promotion of apoptotic cell death and PEA3-mediated transcriptional repression of Her2/neu (erbB-2) oncogene

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Bax cleavage implicates caspase-dependent H2O2-induced apoptosis of hepatocytes

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Orlistat in the treatment of obesity

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Folate receptor α associated with triple-negative breast cancer and poor prognosis

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Identifiers

10.1158/1535-7163.MCT-15-0579

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29 February 2020

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29 February 2020

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