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Authors established a preclinical model of resistance to induction therapy to examine the functional relevance of TFDP3 to chemoresistance in MRD derived from Jurkat/E6-1.
TFDP3 can bind to E2F1 (显示 E2F1 抗体) molecule to form E2F (显示 E2F1 抗体)/TFDP3 complex; and the localizations of TFDP3 and E2F1 (显示 E2F1 抗体) molecules and the co-localization were different in different phases of cell cycle in the nucleus and cytoplasm, which indicated that the E2F (显示 E2F1 抗体)/TFDP3 complex involved in the process of regulating the cell cycle.
data highlight that TFDP3 is expressed in breast cancer, that it is a member of the cancer-testis antigen family and that it functions as a regulator in epithelial-mesenchymal transition
TFDP3 was highly expressed in cancer tissues including prostate cancer tissues.TFDP3 was expressed in coordination with E2F1 (显示 E2F1 抗体) in most prostate cancer tissues.
Data gathered from cell lines, tumorigenicity studies, and primary hepatocellular carcinoma samples demonstrate a negative role of HIF-2alpha (显示 EPAS1 抗体) in tumors, which is mediated by the TFDP3/E2F1 (显示 E2F1 抗体) pathway.
Data show that TFDP3 upregulates the expression of autophagy gene LC3B (显示 MAP1LC3B 抗体) and inhibits E2F1 (显示 E2F1 抗体)-induced apoptosis, and may play an important role in prostate cancer.
DP-4 downregulating E2F-1 (显示 E2F1 抗体) activity and contributes to a new pRb (显示 RB1 抗体)-independent mechanism for regulating cell cycle progression.
TFDP3, a novel DP protein, inhibits DNA binding and transactivation by E2F (显示 E2F1 抗体)
This gene encodes a member of the DP family of transcription factors. These factors heterodimerize with E2F proteins to enhance their DNA-binding activity and promote transcription from E2F target genes. This protein functions as a negative regulator and inhibits the DNA binding and transcriptional activities of E2F factors.
, cancer/testis antigen 30
, hepatocellular carcinoma-associated antigen 661
, transcription factor Dp family member 3
, transcription factor Dp family, member 3