Ctr9, a key subunit of PAFc, affects global estrogen signaling and drives ERα-positive breast tumorigenesis.

Abstract

The human RNA polymerase II (RNAPII)-associated factor complex (hPAFc) and its individual subunits have been implicated in human diseases, including cancer. However, its involvement in breast cancer awaits investigation. Using data mining and human breast cancer tissue microarrays, we found that Ctr9, the key scaffold subunit in hPAFc, is highly expressed in estrogen receptor α-positive (ERα(+)) luminal breast cancer, and the high expression of Ctr9 correlates with poor prognosis. Knockdown of Ctr9 in ERα(+) breast cancer cells almost completely erased estrogen-regulated transcriptional response. At the molecular level, Ctr9 enhances ERα protein stability, promotes recruitment of ERα and RNAPII, and stimulates transcription elongation and transcription-coupled histone modifications. Knockdown of Ctr9, but not other hPAFc subunits, alters the morphology, proliferative capacity, and tamoxifen sensitivity of ERα(+) breast cancer cells. Together, our study reveals that Ctr9, a key subunit of hPAFc, is a central regulator of estrogen signaling that drives ERα(+) breast tumorigenesis, rendering it a potential target for the treatment of ERα(+) breast cancer.

• Authors: Hao Zeng, Wei Xu
• Journal: Genes & development (Genes Dev) Vol. 29 Issue 20 Pg. 2153-67 (Oct 15 2015) ISSN: 1549-5477 [Electronic] United States
• PMID: 26494790 (Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S.)
• Copyright: © 2015 Zeng and Xu; Published by Cold Spring Harbor Laboratory Press.

Chemical References

• Antineoplastic Agents
• CTR9 protein, human
• ESR1 protein, human
• Estrogen Receptor alpha
• Estrogens
• Histones
• Nuclear Proteins
• Phosphoproteins
• Transcription Factors
• Tamoxifen
• RNA Polymerase II

Topics

• Antineoplastic Agents (pharmacology)
• Breast Neoplasms (diagnosis, physiopathology)
• Carcinogenesis (genetics)
• Cell Proliferation
• Data Mining
• Drug Resistance, Neoplasm (genetics)
• Estrogen Receptor alpha (metabolism)
• Estrogens (physiology)
• Female
• Gene Expression Regulation, Neoplastic
• Gene Knockdown Techniques
• Histones (metabolism)
• Humans
• Nuclear Proteins (genetics, metabolism)
• Phosphoproteins (genetics, metabolism)
• Protein Stability
• RNA Polymerase II (metabolism)
• Signal Transduction (genetics)
• Tamoxifen (pharmacology)
• Tissue Array Analysis
• Transcription Elongation, Genetic
• Transcription Factors