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
. 1990;32(2):131-6.
doi: 10.1007/BF01754210.

Common expression of a tumor necrosis factor resistance mechanism among gynecological malignancies

Affiliations

Common expression of a tumor necrosis factor resistance mechanism among gynecological malignancies

C B Powell et al. Cancer Immunol Immunother. 1990.

Abstract

The efficacy of tumor necrosis factor alpha (TNF alpha) as an anticancer agent is limited. This limitation might be related to the expression of a protein-synthesis-dependent resistance mechanism that prevents the lysis of tumor cells by TNF alpha. To test this possibility eight randomly selected human cell lines, three derived from ovarian carcinomas and five derived from cervical carcinomas, were tested for their in vitro sensitivity to TNF alpha-mediated lysis. The results of this analysis showed that all eight cell lines are normally resistant to lysis by TNF alpha. However, in the presence of inhibitors of protein synthesis, seven of them showed a significant increase in TNF alpha-mediated lysis. Measurement of protein synthesis showed that there is a linear correlation between the level of inhibition of protein synthesis and the level of TNF alpha-mediated lysis. The fact that seven of eight randomly selected cell lines are resistant to TNF alpha because they express a protein-synthesis-dependent resistance mechanism suggests that this mechanism of resistance may be common among gynecological cancers. The results also suggest that a therapy involving TNF alpha and inhibitors of protein synthesis might be useful for the treatment of gynecological malignancies.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Aggarawal BB, Moffat B, Harkins RN. Human lymphotoxin. J Biol Chem. 1984;259:686. - PubMed
    1. Blick M, Sherwin SA, Rosenblum M, Gutterman J. Phase I study of recombinant tumor necrosis factor in cancer patients. Cancer Res. 1987;47:2986. - PubMed
    1. Carswell EA, Old LJ, Kassel RL, Green S, Fiore N, Williamson B. An endotoxin induced serum factor that causes necrosis of tumors. Proc Natl Acad Sci USA. 1975;72:3666. - PMC - PubMed
    1. Collins JL, Patek PQ, Cohn M. Tumorigenicity and lysis by natural killers. J Exp Med. 1981;153:89. - PMC - PubMed
    1. Collins JL, Kao M-S, Patek PQ. Humans express natural cytotoxic (NC) cell activity that is similar to murine NC cell activity. J Immunol. 1987;138:4180. - PubMed

MeSH terms