Abstract
Herein, we describe the preparation of liposomes with folate-Targeting properties for the encapsulation of anti-sarcosine antibodies (antisarAbs@LIP) and sarcosine (sar@LIP). The competitive inhibitory effects of exogenously added folic acid supported the role of folate targeting in liposome internalization. We examined the effects of repeated administration on mice PC-3 xenografts. Sar@LIP treatment significantly increased tumor volume and weight compared to controls treated with empty liposomes. Moreover, antisarAbs@LIP administration exhibited a mild antitumor effect. We also identified differences in gene expression patterns post-Treatment. Furthermore, Sar@LIP treatment resulted in decreased amounts of tumor zinc ions and total metallothioneins. Examination of the spatial distribution across the tumor sections revealed a sarcosine-related decline of the MT1X isoform within the marginal regions but an elevation after antisarAbs@LIP administration. Our exploratory results demonstrate the importance of sarcosine as an oncometabolite in PCA. Moreover, we have shown that sarcosine can be a potential target for anticancer strategies in management of PCA.
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CITATION STYLE
Heger, Z., Polanska, H., Merlos Rodrigo, M. A., Guran, R., Kulich, P., Kopel, P., … Adam, V. (2016). Prostate tumor attenuation in the nu/nu murine model due to anti-sarcosine antibodies in folate-Targeted liposomes. Scientific Reports, 6. https://doi.org/10.1038/srep33379
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