Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia

SA. Schubert, D. Ruano, FA. Elsayed, A. Boot, S. Crobach, AF. Sarasqueta, B. Wolffenbuttel, MM. van der Klauw, J. Oosting, CM. Tops, R. van Eijk, HF. Vasen, RH. Vossen, M. Nielsen, S. Castellví-Bel, C. Ruiz-Ponte, I. Tomlinson, MG. Dunlop, P....

. 2017 ; 117 (6) : 1215-1223. [pub] 20170725

Jazyk angličtina Země Anglie, Velká Británie

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc17030669
E-zdroje Online Plný text

NLK Free Medical Journals od 1947 do Před 1 rokem
Freely Accessible Journals od 1947 do Před 1 rokem
PubMed Central od 1947 do Před 1 rokem
Europe PubMed Central od 1947 do Před 1 rokem
ProQuest Central od 2000-01-01 do Před 1 rokem
Open Access Digital Library od 1947-01-01
Open Access Digital Library od 1999-01-01
Nursing & Allied Health Database (ProQuest) od 2000-01-01 do Před 1 rokem
Health & Medicine (ProQuest) od 2000-01-01 do Před 1 rokem
Public Health Database (ProQuest) od 2000-01-01 do Před 1 rokem

BACKGROUND: A substantial fraction of familial colorectal cancer (CRC) and polyposis heritability remains unexplained. This study aimed to identify predisposing loci in patients with these disorders. METHODS: Homozygosity mapping was performed using 222 563 SNPs in 302 index patients with various colorectal neoplasms and 3367 controls. Linkage analysis, exome and whole-genome sequencing were performed in a family affected by microsatellite stable CRCs. Candidate variants were genotyped in 10 554 cases and 21 480 controls. Gene expression was assessed at the mRNA and protein level. RESULTS: Homozygosity mapping revealed a disease-associated region at 1q32.3 which was part of the linkage region 1q32.2-42.2 identified in the CRC family. This includes a region previously associated with risk of CRC. Sequencing identified the p.Asp1432Glu variant in the MIA3 gene (known as TANGO1 or TANGO) and 472 additional rare, shared variants within the linkage region. In both cases and controls the population frequency was 0.02% for this MIA3 variant. The MIA3 mutant allele showed predominant mRNA expression in normal, cancer and precancerous tissues. Furthermore, immunohistochemistry revealed increased expression of MIA3 in adenomatous tissues. CONCLUSIONS: Taken together, our two independent strategies associate genetic variations in chromosome 1q loci and predisposition to familial CRC and polyps, which warrants further investigation.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc17030669
003      
CZ-PrNML
005      
20171030113010.0
007      
ta
008      
171025s2017 enk f 000 0|eng||
009      
AR
024    7_
$a 10.1038/bjc.2017.240 $2 doi
035    __
$a (PubMed)28742792
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a enk
100    1_
$a Schubert, Stephanie A $u Department of Pathology, Leiden University Medical Center, Leiden University, Leiden 2300 RC, The Netherlands.
245    10
$a Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia / $c SA. Schubert, D. Ruano, FA. Elsayed, A. Boot, S. Crobach, AF. Sarasqueta, B. Wolffenbuttel, MM. van der Klauw, J. Oosting, CM. Tops, R. van Eijk, HF. Vasen, RH. Vossen, M. Nielsen, S. Castellví-Bel, C. Ruiz-Ponte, I. Tomlinson, MG. Dunlop, P. Vodicka, JT. Wijnen, FJ. Hes, H. Morreau, NF. de Miranda, RH. Sijmons, T. van Wezel,
520    9_
$a BACKGROUND: A substantial fraction of familial colorectal cancer (CRC) and polyposis heritability remains unexplained. This study aimed to identify predisposing loci in patients with these disorders. METHODS: Homozygosity mapping was performed using 222 563 SNPs in 302 index patients with various colorectal neoplasms and 3367 controls. Linkage analysis, exome and whole-genome sequencing were performed in a family affected by microsatellite stable CRCs. Candidate variants were genotyped in 10 554 cases and 21 480 controls. Gene expression was assessed at the mRNA and protein level. RESULTS: Homozygosity mapping revealed a disease-associated region at 1q32.3 which was part of the linkage region 1q32.2-42.2 identified in the CRC family. This includes a region previously associated with risk of CRC. Sequencing identified the p.Asp1432Glu variant in the MIA3 gene (known as TANGO1 or TANGO) and 472 additional rare, shared variants within the linkage region. In both cases and controls the population frequency was 0.02% for this MIA3 variant. The MIA3 mutant allele showed predominant mRNA expression in normal, cancer and precancerous tissues. Furthermore, immunohistochemistry revealed increased expression of MIA3 in adenomatous tissues. CONCLUSIONS: Taken together, our two independent strategies associate genetic variations in chromosome 1q loci and predisposition to familial CRC and polyps, which warrants further investigation.
650    _2
$a familiární adenomatózní polypóza $x genetika $7 D011125
650    _2
$a receptory aromatických uhlovodíků - jaderný translokátor $x genetika $x metabolismus $7 D051784
650    _2
$a mapování chromozomů $7 D002874
650    _2
$a lidské chromozomy, pár 1 $x genetika $7 D002878
650    _2
$a kolorektální nádory $x genetika $7 D015179
650    _2
$a proteiny aktivující GTPasu $x genetika $x metabolismus $7 D020690
650    _2
$a genetická vazba $7 D008040
650    12
$a genetická predispozice k nemoci $7 D020022
650    _2
$a genotyp $7 D005838
650    _2
$a homozygot $7 D006720
650    _2
$a lidé $7 D006801
650    _2
$a mikrosatelitní repetice $7 D018895
650    _2
$a nádorové proteiny $x genetika $x metabolismus $7 D009363
650    _2
$a jednonukleotidový polymorfismus $7 D020641
650    _2
$a prekancerózy $x genetika $x metabolismus $7 D011230
650    _2
$a messenger RNA $x metabolismus $7 D012333
655    _2
$a časopisecké články $7 D016428
700    1_
$a Ruano, Dina $u Department of Pathology, Leiden University Medical Center, Leiden University, Leiden 2300 RC, The Netherlands.
700    1_
$a Elsayed, Fadwa A $u Department of Pathology, Leiden University Medical Center, Leiden University, Leiden 2300 RC, The Netherlands.
700    1_
$a Boot, Arnoud $u Department of Pathology, Leiden University Medical Center, Leiden University, Leiden 2300 RC, The Netherlands.
700    1_
$a Crobach, Stijn $u Department of Pathology, Leiden University Medical Center, Leiden University, Leiden 2300 RC, The Netherlands.
700    1_
$a Sarasqueta, Arantza Farina $u Department of Pathology, Leiden University Medical Center, Leiden University, Leiden 2300 RC, The Netherlands.
700    1_
$a Wolffenbuttel, Bruce $u Department of Endocrinology, University of Groningen, University Medical Center Groningen, Groningen 9700 RB, The Netherlands.
700    1_
$a van der Klauw, Melanie M $u Department of Endocrinology, University of Groningen, University Medical Center Groningen, Groningen 9700 RB, The Netherlands.
700    1_
$a Oosting, Jan $u Department of Pathology, Leiden University Medical Center, Leiden University, Leiden 2300 RC, The Netherlands.
700    1_
$a Tops, Carli M $u Department of Clinical Genetics, Leiden University Medical Center, Leiden University, Leiden 2300 RC, The Netherlands.
700    1_
$a van Eijk, Ronald $u Department of Pathology, Leiden University Medical Center, Leiden University, Leiden 2300 RC, The Netherlands.
700    1_
$a Vasen, Hans Fa $u Department of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden University, Leiden 2300 RC, The Netherlands.
700    1_
$a Vossen, Rolf Ham $u Department of Human Genetics, Leiden University Medical Center, Leiden University, Leiden 2300 RC, The Netherlands.
700    1_
$a Nielsen, Maartje $u Department of Clinical Genetics, Leiden University Medical Center, Leiden University, Leiden 2300 RC, The Netherlands.
700    1_
$a Castellví-Bel, Sergi $u Department of Gastroenterology, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), University of Barcelona, Barcelona, Catalonia 08036, Spain.
700    1_
$a Ruiz-Ponte, Clara $u Fundación Pública Galega de Medicina Xenómica (FPGMX)-SERGAS, Grupo de Medicina Xenómica-USC, Instituto de Investigación Sanitaria de Santiago (IDIS), Centro de Investigación en Red de Enfermedades Raras (CIBERER), Santiago de Compostela 15706, Spain.
700    1_
$a Tomlinson, Ian $u Oxford Centre for Cancer Gene Research, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK.
700    1_
$a Dunlop, Malcolm G $u Colon Cancer Genetics Group, MRC Human Genetics Unit, The University of Edinburgh, Western General Hospital, Edinburgh EH4 2XU, UK.
700    1_
$a Vodicka, Pavel $u Institute of Experimental Medicine, Institute of Biology and Medical Genetics, Prague 142 00, Czech Republic.
700    1_
$a Wijnen, Juul T $u Department of Clinical Genetics, Leiden University Medical Center, Leiden University, Leiden 2300 RC, The Netherlands.
700    1_
$a Hes, Frederik J $u Department of Clinical Genetics, Leiden University Medical Center, Leiden University, Leiden 2300 RC, The Netherlands.
700    1_
$a Morreau, Hans $u Department of Pathology, Leiden University Medical Center, Leiden University, Leiden 2300 RC, The Netherlands.
700    1_
$a de Miranda, Noel Fcc $u Department of Pathology, Leiden University Medical Center, Leiden University, Leiden 2300 RC, The Netherlands.
700    1_
$a Sijmons, Rolf H $u Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen 9700 RB, The Netherlands.
700    1_
$a van Wezel, Tom $u Department of Pathology, Leiden University Medical Center, Leiden University, Leiden 2300 RC, The Netherlands.
773    0_
$w MED00009369 $t British journal of cancer $x 1532-1827 $g Roč. 117, č. 6 (2017), s. 1215-1223
856    41
$u https://pubmed.ncbi.nlm.nih.gov/28742792 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20171025 $b ABA008
991    __
$a 20171030113059 $b ABA008
999    __
$a ok $b bmc $g 1254262 $s 991696
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2017 $b 117 $c 6 $d 1215-1223 $e 20170725 $i 1532-1827 $m British journal of cancer $n Br J Cancer $x MED00009369
LZP    __
$a Pubmed-20171025

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...