Literature DB >> 34304958

Cell cycle on the crossroad of tumorigenesis and cancer therapy.

Jing Liu1, Yunhua Peng1, Wenyi Wei2.   

Abstract

Aberrancy in cell cycle progression is one of the fundamental mechanisms underlying tumorigenesis, making regulators of the cell cycle machinery rational anticancer therapeutic targets. A growing body of evidence indicates that the cell cycle regulatory pathway integrates into other hallmarks of cancer, including metabolism remodeling and immune escape. Thus, therapies against cell cycle machinery components can not only repress the division of cancer cells, but also reverse cancer metabolism and restore cancer immune surveillance. Besides the ongoing effects on the development of small molecule inhibitors (SMIs) of the cell cycle machinery, proteolysis targeting chimeras (PROTACs) have recently been used to target these oncogenic proteins related to cell cycle progression. Here, we discuss the rationale of cell cycle targeting therapies, particularly PROTACs, to more efficiently retard tumorigenesis.
Copyright © 2021 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  PROTAC; cancer; cancer immune; cell cycle; degradation; metabolism

Mesh:

Year:  2021        PMID: 34304958      PMCID: PMC8688170          DOI: 10.1016/j.tcb.2021.07.001

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  103 in total

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3.  Potent and Preferential Degradation of CDK6 via Proteolysis Targeting Chimera Degraders.

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5.  APC/C-CDH1-Regulated IDH3β Coordinates with the Cell Cycle to Promote Cell Proliferation.

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6.  Development of CDK2 and CDK5 Dual Degrader TMX-2172.

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Review 10.  Mechanisms of CDK4/6 Inhibitor Resistance in Luminal Breast Cancer.

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  18 in total

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4.  Targeting Mitochondrial Oxidative Phosphorylation Eradicates Acute Myeloid Leukemic Stem Cells.

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5.  Immune Landscape and Classification in Lung Adenocarcinoma Based on a Novel Cell Cycle Checkpoints Related Signature for Predicting Prognosis and Therapeutic Response.

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6.  Homologous Recombination Related Signatures Predict Prognosis and Immunotherapy Response in Metastatic Urothelial Carcinoma.

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