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Molecular Glues: The Adhesive Connecting Targeted Protein Degradation to the Clinic

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TLDR
This paper uses data from the CAS Content Collection and the publication landscape of recent research on targeted protein degraders to provide insights into these molecules, with a special focus on molecular glues.
Abstract
Targeted protein degradation is a rapidly exploding drug discovery strategy that uses small molecules to recruit disease-causing proteins for rapid destruction mainly via the ubiquitin–proteasome pathway. It shows great potential for treating diseases such as cancer and infectious, inflammatory, and neurodegenerative diseases, especially for those with “undruggable” pathogenic protein targets. With the recent rise of the “molecular glue” type of protein degraders, which tighten and simplify the connection of an E3 ligase with a disease-causing protein for ubiquitination and subsequent degradation, new therapies for unmet medical needs are being designed and developed. Here we use data from the CAS Content Collection and the publication landscape of recent research on targeted protein degraders to provide insights into these molecules, with a special focus on molecular glues. We also outline the advantages of the molecular glues and summarize the advances in drug discovery practices for molecular glue degraders. We further provide a thorough review of drug candidates in targeted protein degradation through E3 ligase recruitment. Finally, we highlight the progression of molecular glues in drug discovery pipelines and their targeted diseases. Overall, our paper provides a comprehensive reference to support the future development of molecular glues in medicine.

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Approaches to the Management of Metastatic Adenoid Cystic Carcinoma

TL;DR: In this article , the authors summarized the most commonly utilized systemic treatment regimens, review methods of local control for oligometastatic lung disease, and highlight emerging molecular targets with promise for advancing ACC management in the future.
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Protein–protein interfaces in molecular glue-induced ternary complexes: classification, characterization, and prediction

TL;DR: In this paper , a review of known molecular glue-induced ternary complexes and their interface properties is presented, and detailed analysis shows different mechanisms of such structures and computational approaches for predicting protein-protein interfaces.
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An in-silico approach for novel molecular glue design by rationalizing known molecular glue mediated ternary complex formation

TL;DR: This work attempts to establish the rationale for a known case and has inferred the rationale, and discusses how the rationale can be applied in-silico to design novel molecular glue through AI powered techniques.
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Targeted Protein Degradation: Principles and Applications of the Proteasome

TL;DR: The ubiquitin-proteasome system is a multi-catalytic protease complex that is involved in protein quality control via three proteolytic activities (i.e., caspase-, trypsin-, and chymotrypsin-like activities) as mentioned in this paper .
References
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TL;DR: The core Wnt/β-catenin signaling pathway is described, how it controls stem cells, and contributes to disease, and strategies for Wnt-based therapies are discussed.
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TL;DR: Recent findings that indicate CsA and FK506 operate as prodrugs are reviewed: they bind endogenous intracellular receptors, the immunophilins, and the resulting complex targets the protein phosphatase, calcineurin, to exert the immunosuppressive effect.
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The JAZ family of repressors is the missing link in jasmonate signalling

TL;DR: The identification of JASMONATE-INSENSITIVE 3 (JAI3) and a family of related proteins named JAZ (jasmonate ZIM-domain), in Arabidopsis thaliana and the existence of a regulatory feed-back loop involving MYC2 and JAZ proteins, which provides a mechanistic explanation for the pulsed response to jasmonate and the subsequent desensitization of the cell.
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Identification of a Primary Target of Thalidomide Teratogenicity

TL;DR: A basis for thalidomide teratogenicity is revealed and may contribute to the development of new thalidmide derivatives without teratogenic activity.
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A comprehensive map of molecular drug targets

TL;DR: An updated comprehensive map of molecular targets of approved drugs is presented and the relationships between bioactivity class and clinical success, as well as the presence of orthologues between human and animal models and between pathogen and human genomes are explored.