FPGS1 antibodies target the enzyme responsible for polyglutamylation of folates and antifolate drugs, enhancing their intracellular retention and biochemical activity . Key features include:
FPGS1 expression correlates with tumor responsiveness to antifolate therapies like pemetrexed. Studies using NN3.2 demonstrated:
Overexpression in malignancies: 65% of colon adenocarcinoma samples showed 3+ cytoplasmic staining intensity .
Predictive utility: High FPGS1 levels in tumors may indicate better retention of antifolate drugs, improving chemotherapy efficacy .
FPGS1 antibodies have identified isoform-specific roles:
Mitochondrial vs. cytosolic activity: 27616-1-AP confirmed FPGS localization in both compartments, essential for glycine synthesis and nucleotide metabolism .
Gene modulation effects: FPGS1 inhibition reduced THBS2 and C1S expression by 5.25- and 3.26-fold, respectively, altering extracellular matrix dynamics .
| Antibody | Observed Band | Cell Line/Tissue | Reference |
|---|---|---|---|
| NN3.2 | 60 kDa | Ovarian tumor lysates | |
| 27616-1-AP | 65 kDa | HeLa mitochondrial extract | |
| BS-13196R | 59-65 kDa | Breast cancer xenografts |
Normal tissues: Strong reactivity in colon crypts, liver hepatocytes, and lymphoid cells .
Malignant tissues: Heterogeneous cytoplasmic staining, with intensity correlating with tumor grade .
FPGS1 antibodies are pivotal for: