Genetic and Pharmacological Screens Converge in Identifying FLIP, BCL2, and IAP Proteins as Key Regulators of Sensitivity to the TRAIL-Inducing Anticancer Agent ONC201/TIC10-Reference-Cited by-同舟云学术

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Genetic and Pharmacological Screens Converge in Identifying FLIP, BCL2, and IAP Proteins as Key Regulators of Sensitivity to the TRAIL-Inducing Anticancer Agent ONC201/TIC10

Published:2015-02-13 Issue:8 Volume:75 Page:1668-1674
ISSN:0008-5472
Container-title:Cancer Research
language:en
Short-container-title:Cancer Res

Author:

Allen Joshua E.,Prabhu Varun V.,Talekar Mala,van den Heuvel A. Pieter J.,Lim Bora,Dicker David T.,Fritz Jennifer L.,Beck Adam,El-Deiry Wafik S.

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

Cited by 39 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The mitochondrial protease ClpP is a druggable target that controls VSMC phenotype by a SIRT1-dependent mechanism;Redox Biology;2024-07

2. Targeting Mitochondria with ClpP Agonists as a Novel Therapeutic Opportunity in Breast Cancer;Cancers;2023-03-23

3. Therapeutic targeting of TRAIL death receptors;Biochemical Society Transactions;2023-01-11

4. Biological and pharmacological roles of m6A modifications in cancer drug resistance;Molecular Cancer;2022-12-14

5. ONC201-Induced Mitochondrial Dysfunction, Senescence-like Phenotype, and Sensitization of Cultured BT474 Human Breast Cancer Cells to TRAIL;International Journal of Molecular Sciences;2022-12-08

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