bioRxiv · 10.1101/2024.08.01.606147
Loss function of tumor suppressor FRMD8 confers resistance to tamoxifen therapy via a dual mechanism
Abstract
Approximately 40% ER-positive breast cancer patients suffer from therapeutic resistance to tamoxifen. Although reduced ER level is the major cause of tamoxifen resistance, the underlying mechanisms remain elusive. Here, we report that FRMD8 raises the level of ER at both transcriptional and post-translational layers. FRMD8 deficiency in MMTV-Cre+; Frmd8fl/fl; PyMT mice accelerates mammary tumor growth and loss of luminal phenotype, and confers tamoxifen resistance. Single-cell RNA profiling reveals that Frmd8 loss decreases the proportion of hormone-sensing differentiated epithelial cells and downregulates the levels of ER. Mechanically, on one hand, loss of FRMD8 inhibits ESR1 transcription via suppressing the expression of FOXO3A, a transcription factor of ESR1. On the other hand, FRMD8 interacts both with ER and UBE3A, and disrupts the interaction of UBE3A with ER, thereby blocking UBE3A-mediated ER degradation. In breast cancer patients, FRMD8 gene promoter is found hypermethylated and low level of FRMD8 predicts poor prognosis. Therefore, FRMD8 is an important regulator of ER and may control therapeutic sensitivity to tamoxifen in ER-positive breast cancer patients. Impact StatementTumor suppressive protein FRMD8 inhibits breast cancer progression by regulating the level of ER and has the possibility to be a potential target for overcoming tamoxifen treatment resistance.
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Wu, W., Yu, M., Li, Q., Zhao, Y., Zhang, L., Sun, Y., Wang, Z., Gong, Y., Wang, W., Liu, C., Zhang, J., Tang, Y., Xu, X., Guo, X., Zhan, J., Zhang, H.. 2024-08-04. Loss function of tumor suppressor FRMD8 confers resistance to tamoxifen therapy via a dual mechanism. https://doi.org/10.1101/2024.08.01.606147
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