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
. 1999 Jun;80(7):971-80.
doi: 10.1038/sj.bjc.6690451.

Mode of action of thiocoraline, a natural marine compound with anti-tumour activity

Affiliations
Free PMC article

Mode of action of thiocoraline, a natural marine compound with anti-tumour activity

E Erba et al. Br J Cancer. 1999 Jun.
Free PMC article

Abstract

Thiocoraline, a new anticancer agent derived from the marine actinomycete Micromonospora marina, was found to induce profound perturbations of the cell cycle. On both LoVo and SW620 human colon cancer cell lines, thiocoraline caused an arrest in G1 phase of the cell cycle and a decrease in the rate of S phase progression towards G2/M phases, as assessed by using bromodeoxyuridine/DNA biparametric flow cytometric analysis. Thiocoraline does not inhibit DNA-topoisomerase II enzymes in vitro, nor does it induce DNA breakage in cells exposed to effective drug concentrations. The cell cycle effects observed after exposure to thiocoraline appear related to the inhibition of DNA replication. By using a primer extension assay it was found that thiocoraline inhibited DNA elongation by DNA polymerase alpha at concentrations that inhibited cell cycle progression and clonogenicity. These studies indicate that the new anticancer drug thiocoraline probably acts by inhibiting DNA polymerase alpha activity.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Antibiot (Tokyo). 1997 Sep;50(9):734-7 - PubMed
    1. J Antibiot (Tokyo). 1997 Sep;50(9):738-41 - PubMed
    1. Cytometry. 1998 Jan 1;31(1):53-9 - PubMed
    1. Cancer Res. 1976 Jan;36(1):143-50 - PubMed
    1. Cell. 1981 Mar;23(3):647-8 - PubMed

Publication types