ATXN3 promotes breast cancer metastasis by deubiquitinating KLF4. (28th December 2019)
- Record Type:
- Journal Article
- Title:
- ATXN3 promotes breast cancer metastasis by deubiquitinating KLF4. (28th December 2019)
- Main Title:
- ATXN3 promotes breast cancer metastasis by deubiquitinating KLF4
- Authors:
- Zou, Haojing
Chen, Hongyan
Zhou, Zhuan
Wan, Yong
Liu, Zhihua - Abstract:
- Abstract: Krüppel-like factor 4 (KLF4) is an important transcription factor implicated in a variety of essential cellular processes. Aberrant KLF4 expression is closely related to tumourigenesis and tumour progression. The rapid turnover of the KLF4 protein indicates an important role for the posttranslational modifications (PTMs) of KLF4. To date, E3 ligases mediating KLF4 ubiquitination have been widely reported, yet the deubiquitinating mechanism of KLF4 remains largely unknown. We screened a library of 65 deubiquitinating enzymes and identified ATXN3 as a deubiquitinating enzyme of KLF4. Subsequent immunoprecipitation assays confirmed that ATXN3 bound to KLF4, mediating the deubiquitination and stabilization of KLF4 protein levels. Furthermore, we demonstrated that ATXN3 promoted breast cancer cell metastasis via KLF4 in vitro and in vivo . Finally, the protein expression analysis of human breast cancer specimens demonstrated that ATXN3 significantly correlated with KLF4. High ATXN3/KLF4 expression was associated with a poor prognosis in breast cancer patients. Collectively, we identified ATXN3 as a novel deubiquitinating enzyme of KLF4, providing a new explanation for breast cancer metastasis, and proposed ATXN3 as a potential target for breast cancer metastasis treatment. Highlights: ATXN3 deubiquitinates and stabilizes KLF4. ATXN3 promotes breast cancer metastasis by targeting KLF4. ATXN3 expression correlates with KLF4 expression in breast cancer samples. HighAbstract: Krüppel-like factor 4 (KLF4) is an important transcription factor implicated in a variety of essential cellular processes. Aberrant KLF4 expression is closely related to tumourigenesis and tumour progression. The rapid turnover of the KLF4 protein indicates an important role for the posttranslational modifications (PTMs) of KLF4. To date, E3 ligases mediating KLF4 ubiquitination have been widely reported, yet the deubiquitinating mechanism of KLF4 remains largely unknown. We screened a library of 65 deubiquitinating enzymes and identified ATXN3 as a deubiquitinating enzyme of KLF4. Subsequent immunoprecipitation assays confirmed that ATXN3 bound to KLF4, mediating the deubiquitination and stabilization of KLF4 protein levels. Furthermore, we demonstrated that ATXN3 promoted breast cancer cell metastasis via KLF4 in vitro and in vivo . Finally, the protein expression analysis of human breast cancer specimens demonstrated that ATXN3 significantly correlated with KLF4. High ATXN3/KLF4 expression was associated with a poor prognosis in breast cancer patients. Collectively, we identified ATXN3 as a novel deubiquitinating enzyme of KLF4, providing a new explanation for breast cancer metastasis, and proposed ATXN3 as a potential target for breast cancer metastasis treatment. Highlights: ATXN3 deubiquitinates and stabilizes KLF4. ATXN3 promotes breast cancer metastasis by targeting KLF4. ATXN3 expression correlates with KLF4 expression in breast cancer samples. High ATXN3/KLF4 expression is associated with a poor prognosis in breast cancer patients. … (more)
- Is Part Of:
- Cancer letters. Volume 467(2019)
- Journal:
- Cancer letters
- Issue:
- Volume 467(2019)
- Issue Display:
- Volume 467, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 467
- Issue:
- 2019
- Issue Sort Value:
- 2019-0467-2019-0000
- Page Start:
- 19
- Page End:
- 28
- Publication Date:
- 2019-12-28
- Subjects:
- KLF4 -- ATXN3 -- Deubiquitinating enzyme -- Breast cancer -- Metastasis
KLF4 Krüppel-like factor 4 -- PTM posttranslational modification -- UPS ubiquitin-proteasome system -- DUB deubiquitinating enzyme -- CHX cycloheximide
Cancer -- Periodicals
Neoplasms -- Periodicals
Cancer -- Périodiques
Electronic journals
616.994 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03043835/ ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.canlet.2019.09.012 ↗
- Languages:
- English
- ISSNs:
- 0304-3835
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3046.485000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 12013.xml