Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1994 Aug;26(4):393-8.
doi: 10.1007/BF00762780.

Ascorbate on cell growth and differentiation

Affiliations
Review

Ascorbate on cell growth and differentiation

F J Alcaín et al. J Bioenerg Biomembr. 1994 Aug.

Abstract

Ascorbate, an essential nutrient in humans, primates, and guinea pig, is involved in many cellular functions. Ascorbate also modulates cell growth and differentiation. Ascorbate can reduce or stimulate the growth of tumor cells, depending on the cell type. The inhibitory effect is not specific for the biological active isomer L-ascorbate, and isoascorbate and D-ascorbate are more effective in reducing cell growth than L-ascorbate. These results indicate that ascorbate has a cytotoxic effect by killing cells directly, rather a cytostatic one. However, only L-ascorbate is able to stimulate cell growth, but the mechanism of this stimulation is still unknown. L-Ascorbate stimulates the in vitro differentiation of several mesenchyme-derived cell types by altering the expression of multiple genes as the cell progresses through specific differentiation programs. Stimulation of collagen matrix at gene transcription, mRNA stabilization, hydroxylation, and secretion is a key role for L-ascorbate. L-Ascorbate also prevents cell transformation by stabilization of the differentiated state and cooperates with other agents to induce differentiation in a leukemia cell line.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Biochim Biophys Acta. 1987 Sep 11;925(3):258-64 - PubMed
    1. Biochem Biophys Res Commun. 1993 Apr 30;192(2):439-45 - PubMed
    1. Endocr Rev. 1992 Nov;13(4):719-64 - PubMed
    1. Leuk Res. 1991;15(12):1145-52 - PubMed
    1. Nature. 1970 Jul 4;227(5253):24-6 - PubMed

MeSH terms

LinkOut - more resources