HEGER, Zbynek, Jaromír GUMULEC, Natalia CERNEI, Hana POLANSKÁ, Martina RAUDENSKÁ, Michal MASAŘÍK, Tomas ECKSCHLAGER, Marie STIBOROVA, Vojtech ADAM and Rene KIZEK. Relation of exposure to amino acids involved in sarcosine metabolic pathway on behavior of non-tumor and malignant prostatic cell lines. Prostate. Hoboken: Wiley-Blackwell, 2016, vol. 76, No 7, p. 679-690. ISSN 0270-4137. Available from: https://dx.doi.org/10.1002/pros.23159.
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Basic information
Original name Relation of exposure to amino acids involved in sarcosine metabolic pathway on behavior of non-tumor and malignant prostatic cell lines
Authors HEGER, Zbynek (203 Czech Republic), Jaromír GUMULEC (203 Czech Republic, belonging to the institution), Natalia CERNEI (203 Czech Republic), Hana POLANSKÁ (203 Czech Republic, belonging to the institution), Martina RAUDENSKÁ (203 Czech Republic, belonging to the institution), Michal MASAŘÍK (203 Czech Republic, guarantor, belonging to the institution), Tomas ECKSCHLAGER (203 Czech Republic), Marie STIBOROVA (203 Czech Republic), Vojtech ADAM (203 Czech Republic) and Rene KIZEK (203 Czech Republic).
Edition Prostate, Hoboken, Wiley-Blackwell, 2016, 0270-4137.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30200 3.2 Clinical medicine
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 3.820
RIV identification code RIV/00216224:14110/16:00091191
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1002/pros.23159
UT WoS 000373932700007
Keywords in English cancer metabolism; dimethylglycine; folate; glycine; sarcosine pathway; prostate cancer
Tags EL OK
Tags International impact, Reviewed
Changed by Changed by: Ing. Mgr. Věra Pospíšilíková, učo 9005. Changed: 12/10/2016 12:18.
Abstract
BACKGROUND Sarcosine (N-methylglycine) was previously delineated as a substantial oncometabolite of prostate cancer (PCa) and its metabolism seems to be significantly involved in PCa development and behavior. METHODS We focused on investigation whether the exposure of prostate cells (PNT1A, 22Rv1, and PC-3) to sarcosine-related amino acids (glycine, dimethylglycine, and sarcosine) affects their aggressiveness (cell mobility and division rates, using real-time cell based assay). The effect of supplementation on expression of glycine-N-methyltransferase (GNMT) mRNA was examined using qRT-PCR. Finally, post-treatment amino acids patterns were determined with consequent statistical processing using the Ward's method, factorial ANOVA and principal component analysis (P<0.05). RESULTS The highest migration induced sarcosine and glycine in metastatic PC-3 cells (a decrease in relative free area about 53% and 73%). The highest cell division was achieved after treatment of 22Rv1 and PC-3 cells with sarcosine (time required for division decreased by 65% or 45%, when compared to untreated cells). qRT-PCR revealed also significant effects on expression of GNMT. Finally, amino acid profiling shown specific amino acid patterns for each cell line. In both, treated and untreated PC-3 cells significantly higher levels of serine, glutamic acid, and aspartate, linked with prostate cancer progression were found. CONCLUSIONS Sarcosine-related amino acids can exceptionally affect the behavior of benign and malignant prostate cells.
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