Auger electron therapy using In-111-labelled F3 peptide

Auger electron therapy using In-111-labelled F3 peptide

Bibliográfalaš dieđut
Váldodahkkit:	Cornelissen, B, Waller, A, Target, C, Kersemans, V, Smart, S, Vallis, K
Materiálatiipa:	Journal article
Almmustuhtton:	2011

Geahča maid

111In-BnDTPA-F3: an Auger electron-emitting radiotherapeutic agent that targets nucleolin.
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111In-BnDTPA-F3: An Auger electron-emitting radiotherapeutic agent that targets nucleolin
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111In-BnDTPA-F3: An Auger electron-emitting radiotherapeutic agent that targets nucleolin
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ErbB-2 blockade and prenyltransferase inhibition alter epidermal growth factor and epidermal growth factor receptor trafficking and enhance (111)In-DTPA-hEGF Auger electron radiation therapy.
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Targeting the nucleus: an overview of Auger-electron radionuclide therapy.
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Auger electron radionuclide therapy utilising F3 peptide to target the nucleolus
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Properties of [(111)In]-labeled HIV-1 tat peptide radioimmunoconjugates in tumor-bearing mice following intravenous or intratumoral injection.
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(111)In-labeled trastuzumab (Herceptin) modified with nuclear localization sequences (NLS): an Auger electron-emitting radiotherapeutic agent for HER2/neu-amplified breast cancer.
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Biodistribution and nuclear import of 111In-labeled HIV-1 tat peptide immunoconjugates after intravenous or intratumoural injection in tumour-bearing mice
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Relationship between chromatin structure and sensitivity to molecularly targeted auger electron radiation therapy
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Relationship between chromatin structure and sensitivity to molecularly targeted auger electron radiation therapy.
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Trastuzumab-resistant breast cancer cells remain sensitive to the auger electron-emitting radiotherapeutic agent 111In-NLS-trastuzumab and are radiosensitized by methotrexate.
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Methotrexate, paclitaxel, and doxorubicin radiosensitize HER2-amplified human breast cancer cells to the Auger electron-emitting radiotherapeutic agent (111)In-NLS-trastuzumab.
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Epidermal growth factor receptor inhibition modulates the nuclear localization and cytotoxicity of the Auger electron emitting radiopharmaceutical 111In-DTPA human epidermal growth factor.
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Moleculary targeted auger electron radiation therapy for breast cancer: A clinical trial.
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111In-labeled immunoconjugates (ICs) bispecific for the epidermal growth factor receptor (EGFR) and cyclin-dependent kinase inhibitor, p27Kip1.
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Drug-resistant AML cells and primary AML specimens are killed by 111In-anti-CD33 monoclonal antibodies modified with nuclear localizing peptide sequences.
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Indium-111 labeled anti-CD33 monoclonal antibodies (mAbs) modified with nuclear-localizing sequences (NLS) kill mitoxantrone-resistant HL-60 acute myelogenous leukemia (AML) cells
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SPECT imaging and biodistribution studies of 111In-EGF-Au-PEG nanoparticles in vivo
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Cell penetrating peptides for in vivo molecular imaging applications.
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The anti-tumor effect of the auger electron-emitting radiopharmaceutical, In-111-hEGF against MDA-MB-468 human breast cancer xenografts is tumor-size dependent.
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Antitumor Activity of Auger Electron Emitter 111In Delivered by Modular Nanotransporter for Treatment of Bladder Cancer With EGFR Overexpression
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Auger electrons for cancer therapy – a review
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Targeting the tumour: Cell penetrating peptides for molecular imaging and radiotherapy
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Preclinical pharmacokinetic, biodistribution, toxicology, and dosimetry studies of 111In-DTPA-human epidermal growth factor: an auger electron-emitting radiotherapeutic agent for epidermal growth factor receptor-positive breast cancer.
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Preparation and Evaluation of Thermosensitive Liposomes Encapsulating I-125-Labeled Doxorubicin Derivatives for Auger Electron Therapy
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Imaging DNA damage response (DDR) during oncogenesis
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Cellular penetration and nuclear importation properties of 111In-labeled and 123I-labeled HIV-1 tat peptide immunoconjugates in BT-474 human breast cancer cells.
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Single cell S-value calculations of a stochastic cascade model for Auger-electron emitting radionuclides
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Radioimmunotherapy of PANC-1 human pancreatic cancer xenografts in NOD/SCID or NRG mice with Panitumumab labeled with Auger electron emitting, 111In or β-particle emitting, 177Lu
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Monitoring response to anti-angiogenic mTOR inhibitor therapy in vivo using (111)In-bevacizumab.
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Augers and auger bits
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18F-trifluoromethylation of unmodified peptides with 5-18F-(trifluoromethyl)dibenzothiophenium trifluoromethanesulfonate
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Scanning auger electron microscopy /
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The level of insulin growth factor-1 receptor expression is directly correlated with the tumor uptake of (111)In-IGF-1(E3R) in vivo and the clonogenic survival of breast cancer cells exposed in vitro to trastuzumab (Herceptin).
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Targeting the Tumour: Cell Penetrating Peptides for Molecular Imaging and Radiotherapy
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Amplification of DNA damage by a γH2AX-targeted radiopharmaceutical
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Amplification of DNA damage by a γH2AX-targeted radiopharmaceutical.
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Monitoring response to anti-angiogenic mTOR inhibitor therapy in vivo using 111In-bevacizumab
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Internalization of Auger electron-emitting isotopes into cancer cells: A method for spatial distribution determination of equivalent source terms
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