-
Something wrong with this record ?
NAD(P)H:quinone oxidoreductase 1 Pro187Ser polymorphism and expression do not cosegregate with clinico-pathological characteristics of human mammary tumors
M. Hubáčková, R. Václavíková, M. Mrhalová, K. Kubáčková, R. Kodet, I. Gut, P. Souček
Language English Country United States
Document type Research Support, Non-U.S. Gov't
Grant support
NR9426
MZ0
CEP Register
NR8563
MZ0
CEP Register
- MeSH
- Genetic Predisposition to Disease MeSH
- Immunohistochemistry MeSH
- Polymorphism, Single Nucleotide genetics MeSH
- Middle Aged MeSH
- Humans MeSH
- RNA, Messenger genetics metabolism MeSH
- NAD(P)H Dehydrogenase (Quinone) genetics MeSH
- Breast Neoplasms enzymology genetics pathology MeSH
- Proline genetics MeSH
- Gene Expression Regulation, Neoplastic MeSH
- Serine genetics MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Publication type
- Research Support, Non-U.S. Gov't MeSH
OBJECTIVE: The aim of this study was to further clarify the recently reported role of NAD(P)H:quinone oxidoreductase 1 (NQO1) as a strong prognostic and predictive factor in breast cancer. METHODS: NQO1 transcript levels were monitored in mammary tumors by real-time polymerase chain reaction. NQO1 protein levels were immunohistochemically determined in formalin-fixed paraffin-embedded tissues. NQO1 polymorphism (Pro187Ser, rs1800566) was also assessed. Evaluation (N=52) and validation (N=53) sets were analyzed subsequently. RESULTS: Carriers of variant NQO1-Ser allele had significantly more frequently NQO1-negative protein expression (P=0.001) in both sets. NQO1 transcript levels in samples with negative protein expression were significantly lower than in those with positive NQO1 protein expression (P=0.007) in both sets. Patients with stages 0/I/II had more often positive NQO1 protein expression than patients with stages III/IV (P=0.022) in the evaluation set. Significant association between NQO1 protein expression and TP53 protein status was also found (P=0.037). However, both associations were not replicated by analysis of the validation set. Analysis of both sets combined did not show significant association of NQO1 protein expression either with stage (P=0.231) or with TP53 protein status (P>0.999). Thus, the results observed in the evaluation set were effects of small sample size. CONCLUSION: The role of NQO1 in human mammary gland carcinogenesis does not seem to be directly associated with classical clinico-pathological factors.
References provided by Crossref.org
- 000
- 03358naa 2200445 a 4500
- 001
- bmc11019626
- 003
- CZ-PrNML
- 005
- 20170911143848.0
- 008
- 110714s2009 xxu e eng||
- 009
- AR
- 024 __
- $a 10.1097/fpc.0b013e32832cf9cf $2 doi
- 035 __
- $a (PubMed)19494791
- 040 __
- $a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Hubáčková, Miluše. $7 _AN026440
- 245 10
- $a NAD(P)H:quinone oxidoreductase 1 Pro187Ser polymorphism and expression do not cosegregate with clinico-pathological characteristics of human mammary tumors / $c M. Hubáčková, R. Václavíková, M. Mrhalová, K. Kubáčková, R. Kodet, I. Gut, P. Souček
- 314 __
- $a Laboratory of Toxicogenomics, National Institute of Public Health, Prague, Czech Republic.
- 520 9_
- $a OBJECTIVE: The aim of this study was to further clarify the recently reported role of NAD(P)H:quinone oxidoreductase 1 (NQO1) as a strong prognostic and predictive factor in breast cancer. METHODS: NQO1 transcript levels were monitored in mammary tumors by real-time polymerase chain reaction. NQO1 protein levels were immunohistochemically determined in formalin-fixed paraffin-embedded tissues. NQO1 polymorphism (Pro187Ser, rs1800566) was also assessed. Evaluation (N=52) and validation (N=53) sets were analyzed subsequently. RESULTS: Carriers of variant NQO1-Ser allele had significantly more frequently NQO1-negative protein expression (P=0.001) in both sets. NQO1 transcript levels in samples with negative protein expression were significantly lower than in those with positive NQO1 protein expression (P=0.007) in both sets. Patients with stages 0/I/II had more often positive NQO1 protein expression than patients with stages III/IV (P=0.022) in the evaluation set. Significant association between NQO1 protein expression and TP53 protein status was also found (P=0.037). However, both associations were not replicated by analysis of the validation set. Analysis of both sets combined did not show significant association of NQO1 protein expression either with stage (P=0.231) or with TP53 protein status (P>0.999). Thus, the results observed in the evaluation set were effects of small sample size. CONCLUSION: The role of NQO1 in human mammary gland carcinogenesis does not seem to be directly associated with classical clinico-pathological factors.
- 590 __
- $a bohemika - dle Pubmed
- 650 _2
- $a nádory prsu $x enzymologie $x genetika $x patologie $7 D001943
- 650 _2
- $a regulace genové exprese u nádorů $7 D015972
- 650 _2
- $a genetická predispozice k nemoci $7 D020022
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a imunohistochemie $7 D007150
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a NAD(P)H dehydrogenasa (chinon) $x genetika $7 D016660
- 650 _2
- $a jednonukleotidový polymorfismus $x genetika $7 D020641
- 650 _2
- $a prolin $x genetika $7 D011392
- 650 _2
- $a messenger RNA $x genetika $x metabolismus $7 D012333
- 650 _2
- $a serin $x genetika $7 D012694
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Václavíková, Radka $7 xx0142918
- 700 1_
- $a Mrhalová, Marcela $7 xx0062381
- 700 1_
- $a Kubáčková, Kateřina $7 xx0083614
- 700 1_
- $a Kodet, Roman, $d 1953- $7 nlk19990073380
- 700 1_
- $a Gut, Ivan, $d 1936- $7 xx0060370
- 700 1_
- $a Souček, Pavel $7 xx0060511
- 773 0_
- $t Pharmacogenetics and Genomics $w MED00189565 $g Roč. 19, č. 7 (2009), s. 505-512 $x 1744-6872
- 910 __
- $a ABA008 $b x $y 2 $z 0
- 990 __
- $a 20110715114706 $b ABA008
- 991 __
- $a 20170911144453 $b ABA008
- 999 __
- $a ok $b bmc $g 864483 $s 729504
- BAS __
- $a 3
- BMC __
- $a 2009 $x MED00189565 $b 19 $c 7 $d 505-512 $i 1744-6872 $m Pharmacogenetics and genomics $n Pharmacogenet Genomics
- GRA __
- $a NR9426 $p MZ0
- GRA __
- $a NR8563 $p MZ0
- LZP __
- $a 2011-3B09/Bjvme