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

Genetic and epigenetic analysis of the beta-2-microglobulin gene in microsatellite instable colorectal cancer

Z. Snahnicanova, I. Kasubova, M. Kalman, M. Grendar, P. Mikolajcik, E. Gabonova, L. Laca, M. Caprnda, L. Rodrigo, R. Ciccocioppo, P. Kruzliak, L. Plank, Z. Lasabova,

. 2020 ; 20 (1) : 87-95. [pub] 20191218

Jazyk angličtina Země Itálie

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc20028541

Grantová podpora
APVV-16-0066 Agentúra Ministerstva Školstva, Vedy, Výskumu a Športu SR

One of the most common mechanisms of immune evasion in MSI colorectal cancers (CRCs) is loss of HLA class I expression due to mutations in B2M gene which can become a negative predictor for checkpoint blockade therapy. The aim of this study was the determination of prevalence of B2M somatic mutations in MSI CRC patients and relationship between B2M mutations and lymphocytes infiltration and other clinicopathological features as well as detection of methylation changes in B2M promoter region which can be another mechanism of immune escape. In our study, 37 MSI-H and 5 MSI-L patients were selected for screening of B2M mutational and methylation status. The characterization of patients was based on standard histopathological diagnosis and TNM classification; BRAF, KRAS mutations, tumor-infiltrating lymphocytes and peritumoral lymphoid reaction were also determined. MSI analysis was performed using fragment analysis. B2M mutations were identified by Sanger sequencing, and methylation of CpG islands in promoter region was detected by methylation-specific PCR. Heterozygous mutations in the B2M gene were detected in five MSI-H patients (13.5%), while the mutation c.45_48delTTCT was determined in four patients and mutation c.276delC was found in two patients. One of these five patients was compound heterozygote harboring both mutations. Methylation of the promoter region of the B2M gene was observed in one patient with MSI-H colorectal cancer. Detection of genetic and epigenetic changes in B2M gene could be important in personalized therapy for CRC patients as these changes may be one of the mechanisms of secondary resistance of MSI positive tumors to immunotherapy.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc20028541
003      
CZ-PrNML
005      
20210610110946.0
007      
ta
008      
210105s2020 it f 000 0|eng||
009      
AR
024    7_
$a 10.1007/s10238-019-00601-7 $2 doi
035    __
$a (PubMed)31853669
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a it
100    1_
$a Snahnicanova, Zuzana $u Division of Oncology, Biomedical Center Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Mala Hora 4, 036 01, Martin, Slovakia.
245    10
$a Genetic and epigenetic analysis of the beta-2-microglobulin gene in microsatellite instable colorectal cancer / $c Z. Snahnicanova, I. Kasubova, M. Kalman, M. Grendar, P. Mikolajcik, E. Gabonova, L. Laca, M. Caprnda, L. Rodrigo, R. Ciccocioppo, P. Kruzliak, L. Plank, Z. Lasabova,
520    9_
$a One of the most common mechanisms of immune evasion in MSI colorectal cancers (CRCs) is loss of HLA class I expression due to mutations in B2M gene which can become a negative predictor for checkpoint blockade therapy. The aim of this study was the determination of prevalence of B2M somatic mutations in MSI CRC patients and relationship between B2M mutations and lymphocytes infiltration and other clinicopathological features as well as detection of methylation changes in B2M promoter region which can be another mechanism of immune escape. In our study, 37 MSI-H and 5 MSI-L patients were selected for screening of B2M mutational and methylation status. The characterization of patients was based on standard histopathological diagnosis and TNM classification; BRAF, KRAS mutations, tumor-infiltrating lymphocytes and peritumoral lymphoid reaction were also determined. MSI analysis was performed using fragment analysis. B2M mutations were identified by Sanger sequencing, and methylation of CpG islands in promoter region was detected by methylation-specific PCR. Heterozygous mutations in the B2M gene were detected in five MSI-H patients (13.5%), while the mutation c.45_48delTTCT was determined in four patients and mutation c.276delC was found in two patients. One of these five patients was compound heterozygote harboring both mutations. Methylation of the promoter region of the B2M gene was observed in one patient with MSI-H colorectal cancer. Detection of genetic and epigenetic changes in B2M gene could be important in personalized therapy for CRC patients as these changes may be one of the mechanisms of secondary resistance of MSI positive tumors to immunotherapy.
650    _2
$a dospělí $7 D000328
650    _2
$a senioři $7 D000368
650    _2
$a senioři nad 80 let $7 D000369
650    _2
$a kolorektální nádory $x genetika $x patologie $7 D015179
650    _2
$a CpG ostrůvky $7 D018899
650    12
$a metylace DNA $7 D019175
650    _2
$a down regulace $7 D015536
650    _2
$a epigeneze genetická $7 D044127
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a regulace genové exprese u nádorů $7 D015972
650    _2
$a lidé $7 D006801
650    _2
$a mužské pohlaví $7 D008297
650    12
$a mikrosatelitní nestabilita $7 D053842
650    _2
$a lidé středního věku $7 D008875
650    _2
$a mutace $7 D009154
650    _2
$a staging nádorů $7 D009367
650    _2
$a promotorové oblasti (genetika) $7 D011401
650    _2
$a beta-2-mikroglobulin $x genetika $7 D001613
655    _2
$a časopisecké články $7 D016428
700    1_
$a Kasubova, Ivana $u Division of Oncology, Biomedical Center Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Mala Hora 4, 036 01, Martin, Slovakia.
700    1_
$a Kalman, Michal, $u Department of Pathological Anatomy, Jessenius Faculty of Medicine and University Hospital in Martin, Comenius University in Bratislava, Martin, Slovakia. $d 1981- $7 xx0260967
700    1_
$a Grendar, Marian $u Department of Bioinformatics, Biomedical Center Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovakia.
700    1_
$a Mikolajcik, Peter $u Clinic of Surgery and Transplant Center, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovakia.
700    1_
$a Gabonová, Eva $u Clinic of Surgery and Transplant Center, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovakia. $7 xx0257295
700    1_
$a Laca, Ludovit $u Clinic of Surgery and Transplant Center, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovakia.
700    1_
$a Caprnda, Martin $u 1st Department of Internal Medicine, Faculty of Medicine, Comenius University and University Hospital, Bratislava, Slovakia.
700    1_
$a Rodrigo, Luis $u Faculty of Medicine, University of Oviedo, Central University Hospital of Asturias (HUCA), Oviedo, Spain.
700    1_
$a Ciccocioppo, Rachele $u Gastroenterology Unit, Department of Medicine, Azienda Ospedaliera Universitaria, Integrata Policlinico GB Rossi, University of Verona, Verona, Italy.
700    1_
$a Kruzliak, Peter $u Department of Internal Medicine, Brothers of Mercy Hospital, Polní 553/3, 63900, Brno, Czech Republic. kruzliakpeter@gmail.com. 2nd Department of Surgery, Faculty of Medicine, Masaryk University and St. Anne's University Hospital, Brno, Czech Republic. kruzliakpeter@gmail.com.
700    1_
$a Plank, Lukas $u Department of Pathological Anatomy, Jessenius Faculty of Medicine and University Hospital in Martin, Comenius University in Bratislava, Martin, Slovakia.
700    1_
$a Lasabova, Zora $u Division of Oncology, Biomedical Center Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Mala Hora 4, 036 01, Martin, Slovakia. zora.lasabova@uniba.sk. Department of Molecular Biology and Genomics, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovakia. zora.lasabova@uniba.sk.
773    0_
$w MED00006222 $t Clinical and experimental medicine $x 1591-9528 $g Roč. 20, č. 1 (2020), s. 87-95
856    41
$u https://pubmed.ncbi.nlm.nih.gov/31853669 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20210105 $b ABA008
991    __
$a 20210610110945 $b ABA008
999    __
$a ok $b bmc $g 1608876 $s 1119721
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2020 $b 20 $c 1 $d 87-95 $e 20191218 $i 1591-9528 $m Clinical and Experimental Medicine $n Clin Exp Med $x MED00006222
GRA    __
$a APVV-16-0066 $p Agentúra Ministerstva Školstva, Vedy, Výskumu a Športu SR
LZP    __
$a Pubmed-20210105

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...