Academic Journal

Ubiquitin carboxyl-terminal hydrolase isozyme L1/UCHL1 suppresses epithelial-mesenchymal transition and is under-expressed in cadmium-transformed human bronchial epithelial cells

التفاصيل البيبلوغرافية
العنوان: Ubiquitin carboxyl-terminal hydrolase isozyme L1/UCHL1 suppresses epithelial-mesenchymal transition and is under-expressed in cadmium-transformed human bronchial epithelial cells
المؤلفون: Wu, Dan-Dan, Xu, Yan-Ming, Chen, De-Ju, Liang, Zhan-Ling, Chen, Xu-Li, Hylkema, Machteld N, Rots, Marianne G, Li, Sheng-Qing, Lau, Andy T Y
المصدر: Wu , D-D , Xu , Y-M , Chen , D-J , Liang , Z-L , Chen , X-L , Hylkema , M N , Rots , M G , Li , S-Q & Lau , A T Y 2021 , ' Ubiquitin carboxyl-terminal hydrolase isozyme L1/UCHL1 suppresses epithelial-mesenchymal transition and is under-expressed in cadmium-transformed human bronchial epithelial cells ' , Cell biology and toxicology , vol. 37 , no. 4 , pp. 497–513 . https://doi.org/10.1007/s10565-020-09560-2
سنة النشر: 2021
المجموعة: University of Groningen research database
مصطلحات موضوعية: BEAS-2B, Chronic cadmium exposure, Human lung cells, Subcellular proteomics, Ubiquitin carboxyl-terminal hydrolase isozyme L1, Epithelial-mesenchymal transition, TUMOR-SUPPRESSOR, UCHL1 GENE, PROMOTER, PGP9.5, HYPERMETHYLATION, METHYLATION, BIOMARKER, EXPOSURE
الوصف: Cadmium (Cd), a highly toxic heavy metal, is widespreadly distributed in the environment. Chronic exposure to Cd is associated with the development of several diseases including cancers. Over the decade, many researches have been carried on various models to examine the acute effects of Cd; yet, limited knowledge is known about the long-term Cd exposure, especially in the human lung cells. Previously, we showed that chronic Cd-exposed human bronchial epithelial BEAS-2B cells exhibited transformed cell properties, such as anchorage-independent growth, augmented cell migration, and epithelial–mesenchymal transition (EMT). To study these Cd-transformed cells more comprehensively, here, we further characterized their subproteomes. Overall, a total of 63 differentially expressed proteins between Cd-transformed and passage-matched control cells among the five subcellular fractions (cytoplasmic, membrane, nuclear-soluble, chromatin-bound, and cytoskeletal) were identified by mass spectrometric analysis and database searching. Interestingly, we found that the thiol protease ubiquitin carboxyl-terminal hydrolase isozyme L1 (UCHL1) is one of the severely downregulated proteins in the Cd-transformed cells. Notably, the EMT phenotype of Cd-transformed cells can be suppressed by forced ectopic expression of UCHL1, suggesting UCHL1 as a crucial modulator in the maintenance of the proper differentiation status in lung epithelial cells. Since EMT is considered as a critical step during malignant cell transformation, finding novel cellular targets that can antagonize this transition may lead to more efficient strategies to inhibit cancer development. Our data report for the first time that UCHL1 may play a function in the suppression of EMT in Cd-transformed human lung epithelial cells, indicating that UCHL1 might be a new therapeutic target for chronic Cd-induced carcinogenesis. [Figure not available: see fulltext.]
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
DOI: 10.1007/s10565-020-09560-2
الاتاحة: https://hdl.handle.net/11370/6a150b77-f433-45a6-8740-4b293a7b5694
https://research.rug.nl/en/publications/6a150b77-f433-45a6-8740-4b293a7b5694
https://doi.org/10.1007/s10565-020-09560-2
https://pure.rug.nl/ws/files/202902753/Wu2021_Article_UbiquitinCarboxyl_terminalHydr.pdf
Rights: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.A91D9EC1
قاعدة البيانات: BASE
الوصف
DOI:10.1007/s10565-020-09560-2