2006
DOI: 10.1007/s10517-006-0395-6
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In vivo anticancer activity of lysates from Trypanosoma cruzi of different genetic groups

Abstract: Lyzed epimastigotes of Trypanosoma cruzi clones P209-1, Gamba1, Sp104-1, MASu, Y7/1, MN12, Cl-Brener, 86/2036, Y7/2-1 inhibit the growth of Ehrlich adenocarcinoma in mice. the tumor decreased 1.5-3 times after 12 daily injections of lysates from 15 million epimastigotes. The protective effect progressed after the injections were discontinued and depended on the dose and lysate producer clone. Trypanosoma lysates in the studied doses were nontoxic.

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Cited by 16 publications
(6 citation statements)
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“…However, in previous studies, Darani et al (2009) claimed that the crude antigens of T. canis eggs showed antitumor potential. The anti-cancer potential of parasitic products is mostly investigated in crude form; a study by Batmonkh et al (2006) looked at the antitumor properties of parasites ( Trypanosoma cruzi ) in a mouse model in which parasite lysates were able to reduce the tumor size compared to the control group. The present study focused on a specific part of T. canis ES proteins that do not interpret the results as misleading.…”
Section: Discussionmentioning
confidence: 99%
“…However, in previous studies, Darani et al (2009) claimed that the crude antigens of T. canis eggs showed antitumor potential. The anti-cancer potential of parasitic products is mostly investigated in crude form; a study by Batmonkh et al (2006) looked at the antitumor properties of parasites ( Trypanosoma cruzi ) in a mouse model in which parasite lysates were able to reduce the tumor size compared to the control group. The present study focused on a specific part of T. canis ES proteins that do not interpret the results as misleading.…”
Section: Discussionmentioning
confidence: 99%
“…As early as 1948, researchers injected T. cruzi endotoxin directly into tumor-bearing mice, successfully inhibiting the growth of various types of tumors ( Hauschka and Goodwin, 1948 ). Studies involving the lysates of different genetic groups of T. cruzi strains have revealed their notable anti-tumor capabilities ( Sheklakova et al., 2003 ; Batmonkh et al., 2006 ). However, the significant side effects associated with these treatments hinder their direct use in cancer therapy.…”
Section: T Cruzimentioning
confidence: 99%
“…In this complex scenario, where evidence points to both antineoplastic and pro-tumorigenic properties of T. cruzi, it is evident that the interaction of the parasite, its molecules, the host, and cancer involves diverse mechanisms that operate differentially depending on the observational context. The outcome of this intricate interaction depends on various factors: 1) the type of tumor, 2) the virulence and phenotypic characteristics of the T. cruzi strain involved-for instance, some clones exhibit antitumor effects only during infection or immunization, while others exhibit a delayed effect- (Batmonkh et al, 2006), 3) whether the immunogens are parasite lysates or live parasites, and 4) in the case of live parasites, the stage of the disease-acute or chronic phase-regardless of the infected host species.…”
Section: T Cruzi Chagas Disease and Cancer: The Paradox Unveiledmentioning
confidence: 99%