FOXD1 is associated with poor outcome and maintains tumor-promoting enhancer-gene programs in basal-like breast cancer

Breast cancer biology varies markedly among patients. Basal-like breast cancer is one of the most challenging subtypes to treat because it lacks effective therapeutic targets. Despite numerous studies on potential targetable molecules in this subtype, few targets have shown promise. However, the pre...

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Published in:Frontiers in oncology Vol. 13; p. 1156111
Main Authors: Kumegawa, Kohei, Yang, Liying, Miyata, Kenichi, Maruyama, Reo
Format: Journal Article
Language:English
Published: Switzerland Frontiers Media S.A 10-05-2023
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Summary:Breast cancer biology varies markedly among patients. Basal-like breast cancer is one of the most challenging subtypes to treat because it lacks effective therapeutic targets. Despite numerous studies on potential targetable molecules in this subtype, few targets have shown promise. However, the present study revealed that , a transcription factor that functions in both normal development and malignancy, is associated with poor prognosis in basal-like breast cancer. We analyzed publicly available RNA sequencing data and conducted -knockdown experiments, finding that maintains gene expression programs that contribute to tumor progression. We first conducted survival analysis of patients grouped via a Gaussian mixture model based on gene expression in basal-like tumors, finding that is a prognostic factor specific to this subtype. Then, our RNA sequencing and chromatin immunoprecipitation sequencing experiments using the basal-like breast cancer cell lines BT549 and Hs578T with knockdown revealed that regulates enhancer-gene programs related to tumor progression. These findings suggest that plays an important role in basal-like breast cancer progression and may represent a promising therapeutic target.
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These authors have contributed equally to this work
Edited by: Shihori Tanabe, National Institute of Health Sciences (NIHS), Japan
Reviewed by: Jogendra Singh Pawar, The Ohio State University, United States; Anabel Sorolla, Lleida Institute for Biomedical Research (IRBLleida), Spain
ISSN:2234-943X
2234-943X
DOI:10.3389/fonc.2023.1156111