Literature DB >> 28118053

Drain the lysosome: Development of the novel orally available autophagy inhibitor ROC-325.

Jennifer S Carew1, Steffan T Nawrocki1.   

Abstract

Although macroautophagy/autophagy is a key contributor to malignant pathogenesis and therapeutic resistance, there are few FDA-approved agents that significantly affect this pathway. We used medicinal chemistry strategies to develop ROC-325, an orally available novel inhibitor of lysosomal-mediated autophagy. Detailed in vitro and in vivo studies in preclinical models of renal cell carcinoma demonstrated that ROC-325 triggered the hallmark features of lysosomal autophagy inhibition, was very well tolerated, and exhibited significant superiority with respect to autophagy inhibition and anticancer activity over hydroxychloroquine. Our findings support the clinical investigation of the safety and preliminary efficacy of ROC-325 in patients with autophagy-dependent malignancies and other disorders where aberrant autophagy contributes to disease pathogenesis.

Entities:  

Keywords:  ROC-325; autophagy inhibitor; hydroxychloroquine; lucanthone; renal cell carcinoma

Mesh:

Substances:

Year:  2017        PMID: 28118053      PMCID: PMC5388230          DOI: 10.1080/15548627.2017.1280222

Source DB:  PubMed          Journal:  Autophagy        ISSN: 1554-8627            Impact factor:   16.016


  15 in total

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Review 6.  The pleiotropic functions of autophagy in metastasis.

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Review 8.  Targeting Autophagy in Cancer: Update on Clinical Trials and Novel Inhibitors.

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Journal:  bioRxiv       Date:  2020-05-28

Review 10.  Therapeutic Targeting of Autophagy for Renal Cell Carcinoma Therapy.

Authors:  Trace M Jones; Jennifer S Carew; Steffan T Nawrocki
Journal:  Cancers (Basel)       Date:  2020-05-07       Impact factor: 6.575

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