Literature DB >> 31097991

Novel Anthraquinone Compounds Induce Cancer Cell Death through Paraptosis.

Wei Tian1, Junying Li1, Zhengying Su1, Fu Lan1, Zhaoquan Li1, Dandan Liang1, Chunmiao Wang1, Danrong Li2, Huaxin Hou1.   

Abstract

Novel anthraquinone compounds that induce ER stress and paraptosis-like cell death were designed and synthesized. Compound 4a is the first organic micromolecule to kill tumor cells by only paraptosis, and its mechanism of action has been further explored. Paraptosis does not appear to involve either phosphatidylserine translocation associated with apoptosis or cell cycle arrest. The bisbenzyloxy and N-(2-hydroxyethyl)formamide structures may be two critical pharmacophores for paraptosis. Bisbenzyloxy can induce ER stress, and the N-(2-hydroxyethyl)formamide structure can increase the ratio of LC3II/I and cytoplasmic vacuolization and facilitates paraptosis. Some antitumor drugs fail to eradicate malignant cell lines with impaired apoptotic pathways; paraptosis may be a route to kill such cells and provides a new potential strategy for cancer chemotherapy.

Entities:  

Year:  2019        PMID: 31097991      PMCID: PMC6511958          DOI: 10.1021/acsmedchemlett.8b00624

Source DB:  PubMed          Journal:  ACS Med Chem Lett        ISSN: 1948-5875            Impact factor:   4.345


  29 in total

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9.  p62/SQSTM1 binds directly to Atg8/LC3 to facilitate degradation of ubiquitinated protein aggregates by autophagy.

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Journal:  Biochemistry       Date:  2022-04-01       Impact factor: 3.321

2.  Cyclometalated Iridium(III) Complex-Cationic Peptide Hybrids Trigger Paraptosis in Cancer Cells via an Intracellular Ca2+ Overload from the Endoplasmic Reticulum and a Decrease in Mitochondrial Membrane Potential.

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3.  Photosensitization of a subcutaneous tumour by the natural anthraquinone parietin and blue light.

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  6 in total

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