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Co-targeting BET bromodomain BRD4 and RAC1 suppresses growth, stemness and tumorigenesis by disrupting the c-MYC-G9a-FTH1axis and downregulating HDAC1 in molecular subtypes of breast cancer
BET bromodomain BRD4 and RAC1 oncogenes are considered important therapeutic targets for cancer and play key roles in tumorigenesis, survival and metastasis. However, combined inhibition of BRD4-RAC1 signaling pathways in different molecular subtypes of breast cancer including luminal-A, HER-2 posit...
Autores principales: | Ali, Amjad, Shafarin, Jasmin, Unnikannan, Hema, Al-Jabi, Nour, Jabal, Rola Abu, Bajbouj, Khuloud, Muhammad, Jibran Sualeh, Hamad, Mawieh |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8579449/ https://www.ncbi.nlm.nih.gov/pubmed/34803511 http://dx.doi.org/10.7150/ijbs.62236 |
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