PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 19267349-2 2009 After castration, or removal of testicular androgens, CYP17A1 can act as a rate-limiting enzyme in androgen synthesis from cholesterol or other adrenal precursors within the tumor microenvironment ultimately contributing to disease progression. Cholesterol 123-134 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 54-61 19497978-2 2009 Cholesterol side-chain cleavage (CYP11A1) and 17alpha-hydroxylase/17,20-lyase (CYP17) metabolize cholesterol into DHEA, whereas steroid sulfotransferase family 2A1 (SULT2A1) is responsible for conversion of DHEA to DHEA sulfate. Cholesterol 0-11 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 79-84 19497978-2 2009 Cholesterol side-chain cleavage (CYP11A1) and 17alpha-hydroxylase/17,20-lyase (CYP17) metabolize cholesterol into DHEA, whereas steroid sulfotransferase family 2A1 (SULT2A1) is responsible for conversion of DHEA to DHEA sulfate. Cholesterol 97-108 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 79-84 18499961-5 2008 Two of the candidate genes are the CYP17 and the CYP11alpha, encoding the 17-alpha-hydroxylase (P45017alpha) and the cholesterol side chain cleavage (P450scc) respectively. Cholesterol 117-128 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 35-40 9768686-4 1998 After conversion of cholesterol to pregnenolone, 17alpha-hydroxylase/17,20-lyase (CYP17) can metabolize pregnenolone through to DHEA. Cholesterol 20-31 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 82-87 8964847-1 1996 Previous studies of human adrenocortical cells have given inconsistent findings concerning the effects of angiotensin II (AII) alone or in combination with activators of the protein kinase A-signaling pathway on expression of cholesterol side-chain cleavage cytochrome P450 (P450scc), 17 alpha-hydroxylase cytochrome P450 (P450c17), and 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD), as well as the corresponding effects on adrenocortical cell steroid secretory products. Cholesterol 226-237 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 323-330 34333840-3 2021 Abiraterone acetate blocks CYP17A1, which reduces testosterone synthesis from adrenal androgens or cholesterol in the testis, adrenal glands, and prostate cancer cells (2). Cholesterol 99-110 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 27-34 7588323-4 1995 This action of K+ was accompanied by a dose-dependent (P < 0.05 at 6 mM K+ or above) and time-dependent (P < 0.05 at 24 h and beyond) increase in expression of P450c17 and, to a lesser extent, cytochrome P450 cholesterol side-chain cleavage messenger RNA (mRNA). Cholesterol 215-226 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 166-173 8396578-11 1993 IGF-II increased the abundance of ACTH-stimulated mRNAs encoding cholesterol side-chain cleavage cytochrome P450 (P450scc), 17 alpha hydroxylase/17,20 lyase P450 (P450c17), and 3 beta-hydroxysteroid dehydrogenase (3 beta HSD). Cholesterol 65-76 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 163-170 33750894-3 2021 Steroidogenic enzymes, such as CYP11A1, CYP17A1, HSD3B1, AKR1C3 and SRD5A, are essential to catalyze the conversion of the initial substrate cholesterol into potent androgens that confers the CRPC progression. Cholesterol 141-152 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 40-47 2555382-7 1989 Increased P450scc activity, which increased the conversion of cholesterol to pregnenolone, apparently permitted the 17,20-lyase activity of P450c17 to become rate limiting, thus accounting for the increased secretion of 17OHP. Cholesterol 62-73 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 140-147 34041015-5 2021 Based on documentary investigation, we postulated that the AR-SCAP-SREBPs-CYP17/HMGCR axis may regulate cholesterol and androgens synthesis and form a positive enhancement loop promoting NB progression. Cholesterol 104-115 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 74-79 24584631-1 2014 Carbon-carbon bond cleavage reactions are catalyzed by, among others, lanosterol 14-demethylase (CYP51), cholesterol side-chain cleavage enzyme (CYP11), sterol 17beta-lyase (CYP17), and aromatase (CYP19). Cholesterol 105-116 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 174-179 26514241-3 2016 The biosynthesis of cortisol involves a cascade of cholesterol metabolizing reactions regulated through three major CYP proteins: 17alpha-hydroxylase-C17/20-lyase (CYP17), 21-hydroxylase (CYP21), and 11beta-hydroxylase (CYP11B1). Cholesterol 51-62 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 164-169 25334044-6 2014 The mRNA levels of a cholesterol transport protein required for all steroidogenesis, StAR, and steroidogenic enzymes, HSD3beta2, CYP11A1, CYP21A2, and CYP17A1 increased 1.2-2.1-fold in GIP-stimulated H295R-GIPR cells. Cholesterol 21-32 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 151-158 24759590-4 2014 CYP17 is necessary for production of nongonadal androgens from cholesterol. Cholesterol 63-74 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 0-5 22174412-1 2012 TOK-001 and abiraterone are potent 17-heteroarylsteroid (17-HAS) inhibitors of Cyp17, one of the rate-limiting enzymes in the biosynthesis of testosterone from cholesterol in prostate cancer cells. Cholesterol 160-171 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 79-84 22451619-1 2012 Abiraterone acetate is an orally administered potent inhibitor of cytochrome P450, family 17, subfamily A, polypeptide 1 (CYP17), which is essential for synthesis of testosterone from cholesterol. Cholesterol 184-195 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 66-120 22451619-1 2012 Abiraterone acetate is an orally administered potent inhibitor of cytochrome P450, family 17, subfamily A, polypeptide 1 (CYP17), which is essential for synthesis of testosterone from cholesterol. Cholesterol 184-195 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 122-127 22649409-1 2012 Dehydroepiandrosterone (DHEA) is synthesized from cholesterol by activity of P450scc and P450c17, enzymes that we previously characterized in the developing nervous system. Cholesterol 50-61 cytochrome P450 family 17 subfamily A member 1 Homo sapiens 89-96