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A New NT4 Peptide-Based Drug Delivery System for Cancer Treatment

Molecules (Basel, Switzerland), 2020-02, Vol.25 (5), p.1088

2020

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Endocytosis and Trafficking of Heparan Sulfate Proteoglycans in Triple-Negative Breast Cancer Cells Unraveled with a Polycationic Peptide

International journal of molecular sciences, 2020-11, Vol.21 (21), p.8282

2020

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The GAG-specific branched peptide NT4 reduces angiogenesis and invasiveness of tumor cells

PloS one, 2018-03, Vol.13 (3), p.e0194744-e0194744

2018

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Near-infrared quantum dots labelled with a tumor selective tetrabranched peptide for in vivo imaging

Journal of nanobiotechnology, 2018-03, Vol.16 (1), p.21-21, Article 21

2018

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Unraveling Heparan Sulfate Proteoglycan Binding Motif for Cancer Cell Selectivity

Frontiers in oncology, 2019-09, Vol.9, p.843-843

2019

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Heparan Sulfate Proteoglycans Can Promote Opposite Effects on Adhesion and Directional Migration of Different Cancer Cells

Journal of medicinal chemistry, 2020-12, Vol.63 (24), p.15997-16011

2020

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Coupling to a cancer-selective heparan-sulfate-targeted branched peptide can by-pass breast cancer cell resistance to methotrexate

Oncotarget, 2017-09, Vol.8 (44), p.76141-76152

2017

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Insights into the role of sulfated glycans in cancer cell adhesion and migration through use of branched peptide probe

Scientific reports, 2016-06, Vol.6 (1), p.27174-27174, Article 27174

2016

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Abstract 60: Heparan sulfate proteoglycans can mediate cancer cell oriented migration through integrin independent Rac 1 activation

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13_Supplement), p.60-60

2019

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Abstract 1508: Membrane heparan sulfate proteoglycans work with cadherins to establish the directional orientation of migrating cancer cells

Cancer research (Chicago, Ill.), 2024-03, Vol.84 (6_Supplement), p.1508-1508

2024

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Tumor-selective peptide-carrier delivery of Paclitaxel increases in vivo activity of the drug

Scientific reports, 2015-12, Vol.5 (1), p.17736, Article 17736

2015

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Abstract 1153: Heparan sulfate proteoglycans as novel target in cancer precise therapy

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.1153-1153

2017

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Abstract 6312: Targeting HSPG is more efficient than using soluble heparin for interfering with cancer cell adhesion and migration

Cancer research (Chicago, Ill.), 2023-04, Vol.83 (7_Supplement), p.6312-6312

2023

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Abstract 3899: Preclinical development of tetra-branched NT4 peptide theranostics

Cancer research (Chicago, Ill.), 2016-07, Vol.76 (14_Supplement), p.3899-3899

2016

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Cancer Selectivity of Tetrabranched Neurotensin Peptides Is Generated by Simultaneous Binding to Sulfated Glycosaminoglycans and Protein Receptors

Journal of medicinal chemistry, 2013-06, Vol.56 (12), p.5009-5018

2013

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Abstract 5350: Targeting Heparan Sulfated Proteoglycans by branched peptides for selective cancer imaging and therapy

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.5350-5350

2015

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Hyaluronan-based graft copolymers bearing aggregation-induced emission fluorogens

RSC advances, 2018-01, Vol.8 (11), p.5864-5881

2018

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Neurotensin Branched Peptide as a Tumor-Targeting Agent for Human Bladder Cancer

BioMed research international, 2015-01, Vol.2015 (2015), p.1-7

2015

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Abstract 5625: Targeting different LRP receptors and sulfated proteoglycan by branched neurotensin provide high cancer selectivity

Cancer research (Chicago, Ill.), 2013-04, Vol.73 (8_Supplement), p.5625-5625

2013

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Hyaluronan-based graft copolymers bearing aggregation-induced emission fluorogensElectronic supplementary information (ESI) available: Synthetic procedures for the preparation of azide 3 and of model compounds 5 and FA-NEG-OA; 1H NMR spectrum of HA-FA-NEG-OA-8 compared with that of HA-FA-NEG-OA-4; 13C NMR spectrum obtained with HA-FA-NEG-OA-4 derivative compared with those obtained with HA, HA-FA-Pg-3F, and model compound FA-NEG-OA; absorption spectra of compounds 4 and 6. See DOI: 10.1039/c7ra1

2018-02

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A New NT4 Peptide-Based Drug Delivery System for Cancer Treatment

Endocytosis and Trafficking of Heparan Sulfate Proteoglycans in Triple-Negative Breast Cancer Cells Unraveled with a Polycationic Peptide

The GAG-specific branched peptide NT4 reduces angiogenesis and invasiveness of tumor cells

Near-infrared quantum dots labelled with a tumor selective tetrabranched peptide for in vivo imaging

Unraveling Heparan Sulfate Proteoglycan Binding Motif for Cancer Cell Selectivity

Extremely potent human monoclonal antibodies from COVID-19 convalescent patients

Heparan Sulfate Proteoglycans Can Promote Opposite Effects on Adhesion and Directional Migration of Different Cancer Cells

Coupling to a cancer-selective heparan-sulfate-targeted branched peptide can by-pass breast cancer cell resistance to methotrexate

Insights into the role of sulfated glycans in cancer cell adhesion and migration through use of branched peptide probe

Abstract 60: Heparan sulfate proteoglycans can mediate cancer cell oriented migration through integrin independent Rac 1 activation

Abstract 1508: Membrane heparan sulfate proteoglycans work with cadherins to establish the directional orientation of migrating cancer cells

Tumor-selective peptide-carrier delivery of Paclitaxel increases in vivo activity of the drug

Abstract 1153: Heparan sulfate proteoglycans as novel target in cancer precise therapy

Abstract 6312: Targeting HSPG is more efficient than using soluble heparin for interfering with cancer cell adhesion and migration

Abstract 3899: Preclinical development of tetra-branched NT4 peptide theranostics

Cancer Selectivity of Tetrabranched Neurotensin Peptides Is Generated by Simultaneous Binding to Sulfated Glycosaminoglycans and Protein Receptors

Abstract 5350: Targeting Heparan Sulfated Proteoglycans by branched peptides for selective cancer imaging and therapy

Hyaluronan-based graft copolymers bearing aggregation-induced emission fluorogens

Neurotensin Branched Peptide as a Tumor-Targeting Agent for Human Bladder Cancer

Abstract 5625: Targeting different LRP receptors and sulfated proteoglycan by branched neurotensin provide high cancer selectivity

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