2013
Sarcosine as a Potential Prostate Cancer Biomarker-A Review
CERNEI, Natalia Vladimirovna, Zbynek HEGER, Jaromír GUMULEC, Ondřej ZITKA, Michal MASAŘÍK et. al.Základní údaje
Originální název
Sarcosine as a Potential Prostate Cancer Biomarker-A Review
Autoři
CERNEI, Natalia Vladimirovna (498 Moldavsko), Zbynek HEGER (203 Česká republika), Jaromír GUMULEC (203 Česká republika, domácí), Ondřej ZITKA (203 Česká republika), Michal MASAŘÍK (203 Česká republika, garant, domácí), Petr BABULA (203 Česká republika), Tomas ECKSCHLAGER (203 Česká republika), Marie STIBOROVA (203 Česká republika), Rene KIZEK (203 Česká republika) a Vojtech ADAM (203 Česká republika)
Vydání
International Journal of Molecular Sciences, Basel, MDPI Center, 2013, 1422-0067
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10600 1.6 Biological sciences
Stát vydavatele
Švýcarsko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 2.339
Kód RIV
RIV/00216224:14110/13:00070630
Organizační jednotka
Lékařská fakulta
UT WoS
000322171700060
Klíčová slova anglicky
cancer of prostate; biomarkers; early diagnostic; prostatic specific antigen; non-invasive markers; urine; amino acids
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 19. 12. 2013 18:11, Soňa Böhmová
Anotace
V originále
Prostate cancer (CaP) is the most common type of tumour disease in men. Early diagnosis of cancer of the prostate is very important, because the sooner the cancer is detected, the better it is treated. According to that fact, there is great interest in the finding of new markers including amino acids, proteins or nucleic acids. Prostate specific antigen (PSA) is commonly used and is the most important biomarker of CaP. This marker can only be detected in blood and its sensitivity is approximately 80%. Moreover, early stages cannot be diagnosed using this protein. Currently, there does not exist a test for diagnosis of early stages of prostate cancer. This fact motivates us to find markers sensitive to the early stages of CaP, which are easily detected in body fluids including urine. A potential is therefore attributed to the non-protein amino acid sarcosine, which is generated by glycine-N-methyltransferase in its biochemical cycle. In this review, we summarize analytical methods for quantification of sarcosine as a CaP marker. Moreover, pathways of the connection of synthesis of sarcosine and CaP development are discussed.