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
. 1994;33(5):385-90.
doi: 10.1007/BF00686267.

Apoptosis induced by etoposide in small-cell lung cancer cell lines

Affiliations

Apoptosis induced by etoposide in small-cell lung cancer cell lines

S Okamoto-Kubo et al. Cancer Chemother Pharmacol. 1994.

Abstract

The DNA fragmentation, a parameter of apoptosis, in non-small (NSCLC) and small (SCLC) cell lung cancer cell lines (N231 and PC-9) was evaluated. The DNA fragmentation in SCLC lines, but not in NSCLC lines, was observed in overgrown cells without exposure to anticancer drugs. In etoposide (VP-16)-treated N231 but not PC-9 cells, DNA fragmentation continued to increase up to 42 h, and the increase was dependent on the concentration of VP-16. The endonuclease activity of VP-16-treated N231, but not PC-9, cells required both Ca2+ and Mg2+ for full activity. It was elevated in a time- and concentration-dependent manner. As this activity was not affected by addition of cycloheximide, the activation of the endonuclease activity without protein synthesis may be involved in VP-16-induced cytotoxicity in N231.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Int Rev Cytol. 1980;68:251-306 - PubMed
    1. Biochem Biophys Res Commun. 1993 Apr 15;192(1):30-6 - PubMed
    1. J Biol Chem. 1982 Nov 10;257(21):13114-9 - PubMed
    1. Proc Natl Acad Sci U S A. 1992 Aug 15;89(16):7703-7 - PubMed
    1. Exp Cell Res. 1992 Jun;200(2):416-24 - PubMed

Publication types

MeSH terms