-
Je něco špatně v tomto záznamu ?
The expression profile of ATP-binding cassette transporter genes in breast carcinoma
V. Hlaváč, V. Brynychová, R. Václavíková, M. Ehrlichová, D. Vrána, V. Pecha, R. Koževnikovová, M. Trnková, J. Gatěk, D. Kopperová, I. Gut, P. Souček,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
NT13679
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
NLK
ProQuest Central
od 2000-02-01 do 2020-12-31
Health & Medicine (ProQuest)
od 2000-02-01 do 2020-12-31
PubMed
23556449
DOI
10.2217/pgs.13.26
Knihovny.cz E-zdroje
- MeSH
- ABC transportéry genetika metabolismus MeSH
- genetické asociační studie MeSH
- karcinom farmakoterapie genetika patologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádory prsu farmakoterapie genetika patologie MeSH
- neoadjuvantní terapie MeSH
- protinádorové látky aplikace a dávkování MeSH
- regulace genové exprese u nádorů MeSH
- stanovení celkové genové exprese MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
AIM: ATP-binding cassette (ABC) transporters contribute to development of resistance to anticancer drugs via ATP-dependent drug efflux. A major goal of our study was to investigate associations between the expression of ABC transporters and outcome of breast carcinoma patients. PATIENTS & METHODS: Transcript levels of all 49 human ABC transporters were determined in post-treatment tumor and non-neoplastic tissue samples from 68 breast carcinoma patients treated by neoadjuvant chemotherapy. Six ABC transporters were then evaluated in independent series of 100 pretreatment patients. RESULTS: ABCA5/6/8/9/10, ABCB1/5/11, ABCC6/9, ABCD2/4, ABCG5 and ABCG8 were significantly downregulated and ABCA2/3/7/12, ABCB2/3/8/9/10, ABCC1/4/5/10/11/12, ABCD1/3, ABCE1, ABCF1/2/3 and ABCG1 were upregulated in post-treatment tumors compared with non-neoplastic tissues. Significant associations of intratumoral levels of ABCC1 and ABCC8 with grade and expression of hormonal receptors were found in both sets of patients. ABCA12, ABCA13 and ABCD2 levels were significantly associated with the response to neoadjuvant chemotherapy in post-treatment patients. Protein expression of ABCA12, ABCC8 and ABCD2 in tumor tissues of patients with breast carcinoma was observed by immunoblotting for the first time. CONCLUSION: ABCA12, ABCA13, ABCC1, ABCC8 and ABCD2 present potential modifiers of progression and response to the chemotherapy of breast carcinoma.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc13031503
- 003
- CZ-PrNML
- 005
- 20190514130447.0
- 007
- ta
- 008
- 131002s2013 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.2217/pgs.13.26 $2 doi
- 035 __
- $a (PubMed)23556449
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Hlaváč, Viktor $u Toxicogenomics Unit, National Institute of Public Health, Prague, Czech Republic. $7 xx0270481
- 245 14
- $a The expression profile of ATP-binding cassette transporter genes in breast carcinoma / $c V. Hlaváč, V. Brynychová, R. Václavíková, M. Ehrlichová, D. Vrána, V. Pecha, R. Koževnikovová, M. Trnková, J. Gatěk, D. Kopperová, I. Gut, P. Souček,
- 520 9_
- $a AIM: ATP-binding cassette (ABC) transporters contribute to development of resistance to anticancer drugs via ATP-dependent drug efflux. A major goal of our study was to investigate associations between the expression of ABC transporters and outcome of breast carcinoma patients. PATIENTS & METHODS: Transcript levels of all 49 human ABC transporters were determined in post-treatment tumor and non-neoplastic tissue samples from 68 breast carcinoma patients treated by neoadjuvant chemotherapy. Six ABC transporters were then evaluated in independent series of 100 pretreatment patients. RESULTS: ABCA5/6/8/9/10, ABCB1/5/11, ABCC6/9, ABCD2/4, ABCG5 and ABCG8 were significantly downregulated and ABCA2/3/7/12, ABCB2/3/8/9/10, ABCC1/4/5/10/11/12, ABCD1/3, ABCE1, ABCF1/2/3 and ABCG1 were upregulated in post-treatment tumors compared with non-neoplastic tissues. Significant associations of intratumoral levels of ABCC1 and ABCC8 with grade and expression of hormonal receptors were found in both sets of patients. ABCA12, ABCA13 and ABCD2 levels were significantly associated with the response to neoadjuvant chemotherapy in post-treatment patients. Protein expression of ABCA12, ABCC8 and ABCD2 in tumor tissues of patients with breast carcinoma was observed by immunoblotting for the first time. CONCLUSION: ABCA12, ABCA13, ABCC1, ABCC8 and ABCD2 present potential modifiers of progression and response to the chemotherapy of breast carcinoma.
- 650 _2
- $a ABC transportéry $x genetika $x metabolismus $7 D018528
- 650 _2
- $a protinádorové látky $x aplikace a dávkování $7 D000970
- 650 _2
- $a nádory prsu $x farmakoterapie $x genetika $x patologie $7 D001943
- 650 _2
- $a karcinom $x farmakoterapie $x genetika $x patologie $7 D002277
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a stanovení celkové genové exprese $7 D020869
- 650 _2
- $a regulace genové exprese u nádorů $7 D015972
- 650 _2
- $a genetické asociační studie $7 D056726
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a neoadjuvantní terapie $7 D020360
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Brynychová, Veronika $u - $7 xx0323150
- 700 1_
- $a Václavíková, Radka $u - $7 xx0142918
- 700 1_
- $a Ehrlichová, Marie $u - $7 xx0067467
- 700 1_
- $a Vrána, David $u - $7 xx0103187
- 700 1_
- $a Pecha, Václav, $u - $d 1948- $7 xx0103675
- 700 1_
- $a Koževniková, Renata $u - $7 xx0137553
- 700 1_
- $a Trnková, Markéta $u - $7 xx0158385
- 700 1_
- $a Gatěk, Jiří, $u - $d 1950- $7 xx0052958
- 700 1_
- $a Kopperová, Dana $u -
- 700 1_
- $a Gut, Ivan, $u - $d 1936- $7 xx0060370
- 700 1_
- $a Souček, Pavel $u - $7 xx0060511
- 773 0_
- $w MED00008477 $t Pharmacogenomics $x 1744-8042 $g Roč. 14, č. 5 (2013), s. 515-529
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/23556449 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20131002 $b ABA008
- 991 __
- $a 20190514130551 $b ABA008
- 999 __
- $a ok $b bmc $g 995590 $s 829948
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2013 $b 14 $c 5 $d 515-529 $i 1744-8042 $m Pharmacogenomics $n Pharmacogenomics $x MED00008477
- GRA __
- $a NT13679 $p MZ0
- LZP __
- $a Pubmed-20131002