Literature DB >> 9192836

Increased facilitated transport of dehydroascorbic acid without changes in sodium-dependent ascorbate transport in human melanoma cells.

C Spielholz1, D W Golde, A N Houghton, F Nualart, J C Vera.   

Abstract

Many cell types transport vitamin C solely in its oxidized form, dehydroascorbic acid, through facilitative glucose transporters. These cells accumulate large intracellular concentrations of vitamin C by reducing dehydroascorbic acid to ascorbate, a form that is trapped intracellularly. Certain specialized cells can transport vitamin C in its reduced form, ascorbate, through a sodium-dependent cotransporter. We found that normal human melanocytes and human malignant melanoma cells are able to transport vitamin C using both mechanisms. Melanoma cell lines transported dehydroascorbic acid at a rate that was at least 10 times greater than the rate of transport by melanocytes, whereas both melanoma cells and melanocytes transported ascorbate with similar efficiency. Dehydroascorbic acid transport was inhibited by deoxyglucose and cytochalasin B, indicating the direct participation of facilitative glucose transporters in the transport of oxidized vitamin C. Melanoma cells accumulated intracellular vitamin C concentrations that were up to 100 times greater than the corresponding extracellular dehydroascorbic acid concentrations, whereas intracellular accumulation of vitamin C by melanocytes never exceeded the extracellular level of dehydroascorbic acid. Melanoma cells transported dehydroascorbic acid through at least two different transporters, each with a distinct K(m), a finding that agreed well with the presence of several glucose transporter isoforms in these cells. Only one kinetic component of ascorbate uptake was identified in both melanocytes and melanoma cells, and ascorbate transport was sodium dependent and inhibited by ouabain. Both cell types were able to accumulate intracellular concentrations of vitamin C that were greater than the extracellular ascorbate concentrations. The data indicate that melanoma cells and normal melanocytes transport vitamin C using two different transport systems. The transport of dehydroascorbic acid is mediated by a facilitated mechanism via glucose transporters, whereas transport of ascorbic acid involves a sodium-ascorbate cotransporter. The differential capacity of melanoma cells to transport the oxidized form of vitamin C reflects the increased expression of facilitative transporters associated with the malignant phenotype.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9192836

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  19 in total

1.  Ascorbate enhances the toxicity of the photodynamic action of Verteporfin in HL-60 cells.

Authors:  Galina G Kramarenko; Werner W Wilke; Disha Dayal; Garry R Buettner; Freya Q Schafer
Journal:  Free Radic Biol Med       Date:  2006-01-19       Impact factor: 7.376

Review 2.  Targeting cancer vulnerabilities with high-dose vitamin C.

Authors:  Bryan Ngo; Justin M Van Riper; Lewis C Cantley; Jihye Yun
Journal:  Nat Rev Cancer       Date:  2019-05       Impact factor: 60.716

Review 3.  Regulation of the Epigenome by Vitamin C.

Authors:  Juan I Young; Stephan Züchner; Gaofeng Wang
Journal:  Annu Rev Nutr       Date:  2015-05-06       Impact factor: 11.848

4.  Vitamin C Sensitizes Melanoma to BET Inhibitors.

Authors:  Sushmita Mustafi; Vladimir Camarena; Claude-Henry Volmar; Tyler C Huff; David W Sant; Shaun P Brothers; Zhao-Jun Liu; Claes Wahlestedt; Gaofeng Wang
Journal:  Cancer Res       Date:  2017-11-27       Impact factor: 12.701

5.  [(11)C]Ascorbic and [(11)C]dehydroascorbic acid, an endogenous redox pair for sensing reactive oxygen species using positron emission tomography.

Authors:  V N Carroll; C Truillet; B Shen; R R Flavell; X Shao; M J Evans; H F VanBrocklin; P J H Scott; F T Chin; D M Wilson
Journal:  Chem Commun (Camb)       Date:  2016-03-10       Impact factor: 6.222

6.  Histidine residues in the Na+-coupled ascorbic acid transporter-2 (SVCT2) are central regulators of SVCT2 function, modulating pH sensitivity, transporter kinetics, Na+ cooperativity, conformational stability, and subcellular localization.

Authors:  Valeska Ormazabal; Felipe A Zuñiga; Elizabeth Escobar; Carlos Aylwin; Alexis Salas-Burgos; Alejandro Godoy; Alejandro M Reyes; Juan Carlos Vera; Coralia I Rivas
Journal:  J Biol Chem       Date:  2010-09-14       Impact factor: 5.157

7.  Vitamin C protects HL60 and U266 cells from arsenic toxicity.

Authors:  Nicos Karasavvas; Juan M Cárcamo; George Stratis; David W Golde
Journal:  Blood       Date:  2005-01-27       Impact factor: 22.113

8.  Dehydroascorbate uptake activity correlates with cell growth and cell division of tobacco bright yellow-2 cell cultures.

Authors:  Nele Horemans; Geert Potters; Leen De Wilde; Roland J Caubergs
Journal:  Plant Physiol       Date:  2003-09       Impact factor: 8.340

9.  Ascorbic acid participates in a general mechanism for concerted glucose transport inhibition and lactate transport stimulation.

Authors:  Maite A Castro; Constanza Angulo; Sebastián Brauchi; Francisco Nualart; Ilona I Concha
Journal:  Pflugers Arch       Date:  2008-05-28       Impact factor: 3.657

10.  A human sodium-dependent vitamin C transporter 2 isoform acts as a dominant-negative inhibitor of ascorbic acid transport.

Authors:  Eugene A Lutsenko; Juan M Carcamo; David W Golde
Journal:  Mol Cell Biol       Date:  2004-04       Impact factor: 4.272

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.