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enhanced expression of the high affinity ascorbic acid transporter SVCT2, which tightly regulates intracellular ascorbic acid concentrations.
mutant KRAS can be bypassed by L-ascorbic acid in an SVCT-2-dependent manner. Furthermore, SVCT-2 in mutant KRAS colon cancer may act as a potent marker for potentiating L-ascorbic acid co-treatment with cetuximab.
These data suggest that both fruit intake and genetic marker in SLC23A2 may play an independent role in chronic lymphocytic leukemia biology.
Ascorbic acid kills cholangiocarcinoma cells via DNA damage, ATP depletion, and inhibition of mTOR (show FRAP1 Proteins) pathway in a SVCT-2 dependent manner.
Our findings show, for the first time, that transporters of the water-soluble vitamin ascorbic acid (i.e., the vitamin C transporters SVCT-1 (show SVCT1 Proteins) and SVCT-2) are differentially expressed along the length of the intestinal tract and that the pattern of expression is mediated, at least in part, by transcriptional and epigenetic mechanism(s) affecting both Slc23a1 and Slc23a2 genes.
Significant methylation changes in the SLC23A2 and NCOR2 regulatory regions.
Vitamin C supplementation significantly increases skeletal muscle SVCT2 protein expression.
ascorbic acid uptake mechanism, kinetics, and regulation by sodium dependent vitamin C transporter (SVCT2) in MDA-MB231, T47D and ZR-75-1 cells.
Together, these data clarify previous inconsistencies in the literature andimplicate SVCT2 as the pericyte ascorbate transporter.
The functional expression of SVCT2 was detected in HEK293 cells.The kinetic analysis suggested that an ascorbate-dependent mechanism accounts for targeted SVCT2 expression in the developing kidney during medullary epithelial cell differentiation.
Our studies demonstrate that the active SVCT2 is expressed in IVD (show IVD Proteins) cells and that the expression of this transporter is regulated by growth factors IGF-1 (show IGF1 Proteins) and dexamethasone
This study found impaired myelination and reduced collagen expression in Sodium-dependent Vitamin C Transporter 2 heterozygous mice (SVCT2(+/-) ) during peripheral nerve development and after peripheral nerve injury.
Data show that phosphorylation of caveolin-1 (show CAV1 Proteins) on Tyr (show TYR Proteins)(14) in microglia induced the internalization of sodium-vitamin C cotransporter 2 (SVCT2).
Study shows that SVCT2 is regulated at the post-transcriptional level by miR (show MLXIP Proteins)-141 and miR (show MLXIP Proteins)-200a during osteogenic differentiation of bone marrow stromal cells.
Results indicate that both the SVCT2 transporter and oxidative stress play a vital role in BMSC attachment, migration and cytoskeletal re-arrangement.
Increased expression of SVCT2 in a new mouse model raises ascorbic acid in tissues and protects against oxidative stress.
the expression and transport activity of SVCT2 in brain capillary endothelial cells after transient ischemia
Expression of various collagen types is reduced in sciatic nerves of SVCT2(+/-) heterozygous mice compared to wild-type.
The results suggest that expression of the SVCT2 is differentially regulated during embryonic development and in adulthood.
Evidence of increased apoptosis in SVCT2(-/-) mice and disruption of the basement membrane in fetal brain.
The absorption of vitamin C into the body and its distribution to organs requires two sodium-dependent vitamin C transporters. This gene encodes one of the two required transporters and the encoded protein accounts for tissue-specific uptake of vitamin C. Previously, this gene had an official symbol of SLC23A1.
Na(+)/L-ascorbic acid transporter 2
, nucleobase transporter-like 1 protein
, sodium-dependent vitamin C transporter-2
, solute carrier family 23 (nucleobase transporters), member 1
, solute carrier family 23 (nucleobase transporters), member 2
, solute carrier family 23 member 2
, yolk sac permease-like molecule 2
, sodium-coupled ascorbic acid transporter 2
, sodium-dependent vitamin C transporter 2
, sodium-coupled ascorbic acid transporter SVCT2