Literature DB >> 31508966

A Novel Conjugate of Bis[((4-bromophenyl)amino)quinazoline], a EGFR-TK Ligand, with a Fluorescent Ru(II)-Bipyridine Complex Exhibits Specific Subcellular Localization in Mitochondria.

Rashid Ilmi1, Eleni Tseriotou, Panayiota Stylianou1, Yiota A Christou1, Iakovia Ttofi, Nikolas Dietis, Costas Pitris, Andreani D Odysseos1, Savvas N Georgiades.   

Abstract

The epidermal growth factor receptor (EGFR) is a key target in anticancer research, whose aberrant function in malignancies has been linked to severe irregularities in critical cellular processes, including cell cycle progression, proliferation, differentiation, and survival. EGFR mutant variants, either transmembrane or translocated to the mitochondria and/or the nucleus, often exhibit resistance to EGFR inhibitors. The ability to noninvasively image and quantify EGFR provides novel approaches in the detection, monitoring, and treatment of EGFR-related malignancies. The current study aimed to deliver a new theranostic agent that combines fluorescence imaging properties with EGFR inhibition. This was achieved via conjugation of an in-house-developed ((4-bromophenyl)amino)quinazoline inhibitor of mutant EGFR-TK, selected from a focused aminoquinazoline library, with a [Ru(bipyridine)3]2+ fluorophore. A triethyleneglycol-derived diamino linker featuring (+)-ionizable sites was employed to link the two functional moieties, affording two unprecedented Ru conjugates with 1:1 and 2:1 stoichiometry of aminoquinazoline to the Ru complex (mono-quinazoline-Ru-conjugate and bis-quinazoline-Ru-conjugate, respectively). The bis-quinazoline-Ru-conjugate, which retains an essential inhibitory activity, was found by fluorescence imaging to be effectively uptaken by Uppsala 87 malignant glioma (grade IV malignant glioma) cells. The fluorescence imaging study and a time-resolved fluorescence resonance energy transfer study indicated a specific subcellular distribution of the conjugate that coincides with that of a mitochondria-targeted dye, suggesting mitochondrial localization of the conjugate and potential association with mitochondria-translocated forms of EGFR. Mitochondrial localization was further documented by the specific concentration of the bis-quinazoline-Ru-conjugate in a mitochondrial isolation assay.

Entities:  

Keywords:  TEG linker; aminoquinazoline; epidermal growth factor receptor tyrosine kinase; mitocan; mitochondrial localization; ruthenium conjugate

Mesh:

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Year:  2019        PMID: 31508966     DOI: 10.1021/acs.molpharmaceut.9b00608

Source DB:  PubMed          Journal:  Mol Pharm        ISSN: 1543-8384            Impact factor:   4.939


  3 in total

Review 1.  Emerging Molecular Receptors for the Specific-Target Delivery of Ruthenium and Gold Complexes into Cancer Cells.

Authors:  João Franco Machado; João D G Correia; Tânia S Morais
Journal:  Molecules       Date:  2021-05-25       Impact factor: 4.411

2.  Hydrogen peroxide-mediated synthesis of 2,4-substituted quinazolines via one-pot three-component reactions under metal-free conditions.

Authors:  Khang H Trinh; Khang X Nguyen; Phuc H Pham; Tung T Nguyen; Anh N Q Phan; Nam T S Phan
Journal:  RSC Adv       Date:  2020-08-13       Impact factor: 3.361

Review 3.  Molecular Targeting of Epidermal Growth Factor Receptor (EGFR) and Vascular Endothelial Growth Factor Receptor (VEGFR).

Authors:  Nichole E M Kaufman; Simran Dhingra; Seetharama D Jois; Maria da Graça H Vicente
Journal:  Molecules       Date:  2021-02-18       Impact factor: 4.411

  3 in total

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