Abstract | BACKGROUND: METHODS: The role of STAT3 in Pol I-directed transcription was determined using combined techniques. The regulation of tumor cell growth mediated by STAT3 and Pol I products was analyzed in vitro and in vivo. RNAseq, ChIP assays and rescue assays were used to uncover the mechanism of Pol I transcription mediated by STAT3. RESULTS: STAT3 expression positively correlates with Pol I product levels and cancer cell growth. The inhibition of STAT3 or Pol I products suppresses cell growth. Mechanistically, STAT3 activates Pol I-directed transcription by enhancing the recruitment of the Pol I transcription machinery to the rDNA promoter. STAT3 directly activates Rpa34 gene transcription by binding to the RPA34 promoter, which enhances the occupancies of the Pol II transcription machinery factors at this promoter. Cancer patients with RPA34 high expression lead to poor survival probability and short survival time. CONCLUSION: STAT3 potentiates Pol I-dependent transcription and tumor cell growth by activating RPA34 in vitro and in vivo.
|
Authors | Cheng Zhang, Juan Wang, Xiaoye Song, Deen Yu, Baoqiang Guo, Yaoyu Pang, Xiaomei Yin, Shasha Zhao, Huan Deng, Shihua Zhang, Wensheng Deng |
Journal | British journal of cancer
(Br J Cancer)
Vol. 128
Issue 5
Pg. 766-782
(03 2023)
ISSN: 1532-1827 [Electronic] England |
PMID | 36526675
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Copyright | © 2022. The Author(s), under exclusive licence to Springer Nature Limited. |
Chemical References |
- RNA Polymerase I
- RNA Polymerase II
- STAT3 protein, human
- STAT3 Transcription Factor
|
Topics |
- Humans
- Promoter Regions, Genetic
- RNA Polymerase I
(genetics)
- RNA Polymerase II
(genetics, metabolism)
- STAT3 Transcription Factor
(metabolism)
- Transcription, Genetic
|