A central role for TRPS1 in the control of cell cycle and cancer development

The eukaryotic cell cycle is controlled by a complex regulatory network, which is still poorly understood. Here we demonstrate that TRPS1, an atypical GATA factor, modulates cell proliferation and controls cell cycle progression. Silencing TRPS1 had a differential effect on the expression of nine key cell cycle-related genes. Eight of these genes are known to be involved in the regulation of the G2 phase and the G2/M transition of the cell cycle. Using cell synchronization studies, we confirmed that TRPS1 plays an important role in the control of cells in these phases of the cell cycle. We also show that silencing TRPS1 controls the expression of 53BP1, but not TP53. TRPS1 silencing also decreases the expression of two histone deacetylases, HDAC2 and HDAC4, as well as the overall HDAC activity in the cells, and leads to the subsequent increase in the acetylation of histone4 K16 but not of histone3 K9 or K18. Finally, we demonstrate that TRPS1 expression is elevated in luminal breast cancer cells and luminal breast cancer tissues as compared with other breast cancer subtypes. Overall, our study proposes that TRPS1 acts as a central hub in the control of cell cycle and proliferation during cancer development.

Medienart:

E-Artikel

Erscheinungsjahr:

2014

Erschienen:

2014

Enthalten in:

Zur Gesamtaufnahme - volume:5

Enthalten in:

Oncotarget - 5(2014), 17 vom: 15. Sept., Seite 7677-90

Sprache:

Englisch

Beteiligte Personen:

Wu, Lele [VerfasserIn]
Wang, Yuzhi [VerfasserIn]
Liu, Yan [VerfasserIn]
Yu, Shiyi [VerfasserIn]
Xie, Hao [VerfasserIn]
Shi, Xingjuan [VerfasserIn]
Qin, Sheng [VerfasserIn]
Ma, Fei [VerfasserIn]
Tan, Tuan Zea [VerfasserIn]
Thiery, Jean Paul [VerfasserIn]
Chen, Liming [VerfasserIn]

Themen:

DNA-Binding Proteins
Journal Article
RNA, Small Interfering
Repressor Proteins
Research Support, Non-U.S. Gov't
TRPS1 protein, human
Transcription Factors

Anmerkungen:

Date Completed 06.08.2015

Date Revised 21.10.2021

published: Print

Citation Status MEDLINE

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM242426379