E3 ubiquitin ligase ITCH-mediated proteasomal degradation of WBP2 sensitizes breast cancer cells to chemotherapy through restraining AMOTL2/c-JUN axis
- 19 December 2024
- journal article
- research article
- Published by Elsevier in Biochemical Pharmacology
- Vol. 232, 116720
Abstract
No abstract availableKeywords
This publication has 50 references indexed in Scilit:
- Induced expression of AMOT reverses adriamycin resistance in breast cancer cellsCell Biology International, 2024
- Potential role of CXCR4 in trastuzumab resistance in breast cancer patientsBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 2022
- WBP2 promotes BTRC mRNA stability to drive migration and invasion in triple‐negative breast cancer via NF‐κB activationMolecular Oncology, 2021
- Neoadjuvant chemotherapy for luminal a breast cancer: Factors predictive of histopathologic response and oncologic outcomeThe American Journal of Surgery, 2021
- Itch attenuates CD4 T‐cell proliferation in mice by limiting WBP2 protein stabilityEuropean Journal of Immunology, 2020
- Regulation of autoimmune disease by the E3 ubiquitin ligase ItchCellular Immunology, 2019
- ASPP2 suppresses invasion and TGF-β1-induced epithelial–mesenchymal transition by inhibiting Smad7 degradation mediated by E3 ubiquitin ligase ITCH in gastric cancerCancer Letters, 2017
- WBP2 modulates G1/S transition in ER+ breast cancer cells and is a direct target of miR-206Cancer Chemotherapy and Pharmacology, 2017
- The HECT Family of E3 Ubiquitin Ligases: Multiple Players in Cancer DevelopmentCancer Cell, 2008
- The Nedd4-like family of E3 ubiquitin ligases and cancerCancer and Metastasis Reviews, 2007