FILIP1L antibodies are immunoreagents designed to bind specifically to the FILIP1L protein, a regulator of the WNT/β-catenin pathway and epithelial-to-mesenchymal transition (EMT). FILIP1L acts as a tumor suppressor by promoting β-catenin degradation, inhibiting metastasis, and enhancing chemosensitivity in cancers such as ovarian and colorectal carcinomas . Antibodies targeting FILIP1L are widely used in techniques like immunohistochemistry (IHC), Western blotting (WB), and immunofluorescence (IF) to study its expression and function.
FILIP1L antibodies are pivotal in elucidating the protein’s role in cancer progression and therapeutic response. Below are key applications supported by experimental data:
Low FILIP1L expression correlates with advanced tumor stage, chemoresistance, and poor survival .
Antibody-based IHC on 369 ovarian samples confirmed FILIP1L’s inverse relationship with β-catenin and EMT markers (e.g., SNAIL, SLUG) .
FILIP1L knockdown in CRC cells (e.g., COLO205) enhances migration, invasion, and angiogenesis, while overexpression (e.g., HCT116) induces apoptosis and cell cycle arrest .
IHC of patient tissues revealed FILIP1L’s association with reduced tumor size, lymph node metastasis, and improved survival .
Overexpression of FILIP1L in endothelial cells inhibits proliferation, migration, and tumor neovascularization .
Truncated FILIP1L mutants (e.g., FILIP1LΔC103) suppress melanoma growth by targeting tumor vasculature .
FILIP1L promotes β-catenin phosphorylation and proteasomal degradation, thereby inhibiting WNT target genes (e.g., MMP3, MMP9) and EMT .
In CRC, FILIP1L inactivation elevates Akt/GSK-3β signaling, driving angiogenesis via VEGF-A and HIF-1α upregulation .
Ovarian Cancer: FILIP1L overexpression in orthotopic mouse models reduced peritoneal metastases by 7–16 fold .
Colorectal Cancer: FILIP1L knockout mice exhibited colonic hyperplasia and mucin hypersecretion, mimicking human mucinous adenocarcinoma .