CCNE1 antibodies are immunological reagents designed to bind specifically to the Cyclin E1 protein, a key regulator of the G1-to-S phase transition in the cell cycle. CCNE1 forms a complex with CDK2 to initiate DNA replication and cell division . These antibodies are used in techniques such as:
Western blotting (WB)
Immunohistochemistry (IHC-P)
Flow cytometry
Immunofluorescence (IF)
| Antibody Name | Host Species | Applications | Specificity Confirmed By |
|---|---|---|---|
| Anti-CCNE1 [CCNE1/2460] | Mouse | WB, IHC-P | HuProt protein array |
| 11554-1-AP | Rabbit | WB, IHC, IP | U2OS/MDA-MB-231 cells |
CCNE1 overexpression drives uncontrolled cell proliferation by:
Promoting premature S-phase entry, leading to genomic instability
Enhancing epithelial-mesenchymal transition (EMT) and metastasis
Studies using CCNE1 antibodies have revealed its interaction with CDK2 and its role in activating the MMB–FOXM1 mitotic transcriptional program, which accelerates cell division .
Overexpression correlates with poor survival in breast (BRCA), lung (LUAD), liver (LIHC), and ovarian cancers .
Immune microenvironment modulation: High CCNE1 levels associate with increased cancer-associated fibroblasts in BRCA, COAD, and STAD tumors .
CCNE1 immunohistochemistry does not predict taxane-platinum chemoresistance in ovarian cancer, challenging earlier hypotheses .
CCNE1 expression positively correlates with TMB, MSI, and immune checkpoint markers (e.g., PD-1, CTLA-4), suggesting immunotherapy implications .
Xenograft studies: RP-6306 (PKMYT1 inhibitor) achieves 84% tumor regression in CCNE1-amplified OVCAR3 models .
Patient-derived organoids: CCNE1 amplification sensitizes tumors to CDK1-targeted therapies .