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
. 1984;18(1):49-53.
doi: 10.1007/BF00205399.

Antitumor and antimetastatic activity of the immunoadjuvant peptidoglycan monomer PGM in mice bearing MCa mammary carcinoma

Antitumor and antimetastatic activity of the immunoadjuvant peptidoglycan monomer PGM in mice bearing MCa mammary carcinoma

G Sava et al. Cancer Immunol Immunother. 1984.

Abstract

The antitumor and antimetastatic activities of the water-soluble peptidoglycan monomer GlnNAc-Mur-NAc-L-Ala-D-iso-Gln-meso-diamminopimelic acid (omega-NH2)-D-Ala-D-Ala (PGM), which has immunostimulant effects, have been evaluated in CBA mice bearing MCa mammary carcinoma. The antineoplastic effects of PGM depend strictly on the dosage and treatment schedule used. Though a significant inhibition of the primary tumor growth is observed over a wide range of dosage, only the IV administration of daily doses of 50 mg/kg/day on days 1, 5, 10, 15 inhibits spontaneous lung metastasis formation and in parallel prolongs the survival time of the treated mice. The magnitude of the antimetastatic effects of PGM depends on the degree of dissemination of the tumor, and is greater when the number of metastatic foci is low. Examination of the therapeutic potential of PGM in combination with surgery has further indicated that the timing of administration plays an important role in the overall effectiveness of this substance. A 5-day interval is necessary between two consecutive injections for the induction of significant increases of the survival times.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Baldwin RW. Manipulation of host resistance in cancer therapy. Semin Immunopathol. 1982;5:113–125. - PubMed
    1. Fidler IJ, Sone S, Fogler WE, Barnes ZL. Eradication of spontaneous metastases and activation of alveolar macrophages by intravenous injection of liposomes containing muramyl dipeptide. Proc Natl Acad Sci USA. 1981;78:1680–1684. - PMC - PubMed
    1. Giraldi T, Sava G, Cuman R, Nisi C, Lassiani L. Selectivity of the antimetastatic and cytotoxic effects of p-(3,3-dimethyl-1-triazeno)benzoic acid potassium salt, (±)1,2-di-(3,5-dioxopiperazin-1-yl)propane and cyclophosphamide in mice bearing Lewis lung carcinoma. Cancer Res. 1981;41:2524–2528. - PubMed
    1. Hršak I, Tomašić J, Pavelić K, Valinger Z. Stimulation of humoral immunity by peptidoglycan monomer from Brevibacterium divaricatum . Z Immunitaetsforsch Immunobiol. 1978;155:312–318. - PubMed
    1. Hršak I, Novak D, Tomašić J. Immunostimulating activity of peptidoglycan monomer (PGM) on in vivo primary response to sheep erythrocytes, Salmonella typhymurium and Newcastle disease virus. Period Biol. 1980;82:147–151.

Publication types

Substances

LinkOut - more resources