KAP1 Promotes Proliferation and Metastatic Progression of Breast Cancer Cells
Year: 2014
Type: article
Abstract: KAP1 (TRIM28) is a transcriptional regulator in embryonic development that controls stem cell self-renewal, chromatin organization, and the DNA damage response, acting as an essential corepressor for KRAB family zinc finger proteins (KRAB-ZNF). To gain insight into the function of this large gene family, we developed an antibody that recognizes the conserved zinc fingers linker region (ZnFL) in multiple KRAB-ZNF. Here, we report that the expression of many KRAB-ZNF along with active SUMOlyated KAP1 is elevated widely in human breast cancers. KAP1 silencing in breast cancer cells reduced proliferation and inhibited the growth and metastasis of tumor xenografts. Conversely, KAP1 overexpression stimulated cell proliferation and tumor growth. In cells where KAP1 was silenced, we identified multiple downregulated genes linked to tumor progression and metastasis, including EREG/epiregulin, PTGS2/COX2, MMP1, MMP2, and CD44, along with downregulation of multiple KRAB-ZNF proteins. KAP1-dependent stabilization of KRAB-ZNF required direct interactions with KAP1. Together, our results show that KAP1-mediated stimulation of multiple KRAB-ZNF contributes to the growth and metastasis of breast cancer.
Source: Cancer Research
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
Awards: G1274820946, The role of HEF1/NEDD9 protein in proliferation and invasion of metastatic breast cancer, West Virginia IDeA Network of Biomedical Research Excellence (WV-INBRE), G2461264676, CoBRE for Signal Transduction and Cancer Phase III, Cobre for Signal Transduction and Cancer, CoBRE for Signal Transduction and Cancer Phase III, West Virginia IDeA Network of Biomedical Research Excellence (WV-INBRE), Baylor College of Medicine Cancer Center - Cancer Center Support Grant
OpenAlex ID: W2062364357
