-
Je něco špatně v tomto záznamu ?
Diagnostic and prognostic potential of miR-21, miR-29c, miR-148 and miR-203 in adenocarcinoma and squamous cell carcinoma of esophagus
R. Hezova, A. Kovarikova, J. Srovnal, M. Zemanova, T. Harustiak, J. Ehrmann, M. Hajduch, M. Svoboda, M. Sachlova, O. Slaby,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
NT13585
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
NLK
BioMedCentral
od 2006-12-01
BioMedCentral Open Access
od 2006
Directory of Open Access Journals
od 2006
Free Medical Journals
od 2006
PubMed Central
od 2006
Europe PubMed Central
od 2006
ProQuest Central
od 2009-01-01
Open Access Digital Library
od 2006-01-01
Medline Complete (EBSCOhost)
od 2006-01-01
Health & Medicine (ProQuest)
od 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2006
Springer Nature OA/Free Journals
od 2006-12-01
- MeSH
- adenokarcinom diagnóza genetika MeSH
- lidé středního věku MeSH
- lidé MeSH
- mikro RNA genetika MeSH
- nádorové biomarkery analýza genetika metabolismus MeSH
- nádory jícnu diagnóza genetika MeSH
- prognóza MeSH
- regulace genové exprese u nádorů genetika MeSH
- senioři MeSH
- spinocelulární karcinom diagnóza genetika MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
BACKGROUND: Esophageal cancer is the malignant tumor with very poor prognosis and increasing incidence often diagnosed at very late stage, so the prognosis of affected patients is unsatisfactory, despite the development of therapeutic option such as surgery, chemotherapy and radiotherapy. Consequently, there is a great need for biomarkers to allow a tailored multimodality approach with increased efficiency. Altered expression of microRNAs has been reported in wide range of malignancies, including esophageal cancer. The aim of this study was to examine the expression levels of candidate microRNAs in esophageal cancer and evaluate their diagnostic and prognostic potential. FINDINGS: Using quantitative real-time PCR, expression levels of 9 candidate microRNAs were examined in 62 tissue samples, 23 esophageal adenocarcinomas, 22 esophageal squamous cell carcinomas and 17 adjacent esophageal mucosa samples. MicroRNA expression levels were further analyzed in regards to clinico-pathological features of esophageal cancer patients. We observed significantly decreased levels of miR-203 and increased levels of miR-21 in adenocarcinoma tissues when compared to normal mucosa. MiR-29c and miR-148 indicated good ability to distinguish between histological subtypes of esophageal cancer. MiR-203 and miR-148 were linked to disease-free survival and overall survival in esophageal adenocarcinoma patients, and miR-148 also in esophageal squamous cell carcinoma patients. CONCLUSIONS: Our data suggest that altered expression of miR-21, miR-29c, miR-148 and miR-203 are related to neoplastic transformation and progression of the disease and these microRNAs could serve as a potential diagnostic and prognostic biomarkers in esophageal cancer. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/4646922201567057.
3rd Department of Surgery University Hospital in Motol Prague Czech Republic
Department of Oncology General University Hospital Prague Prague Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc16010247
- 003
- CZ-PrNML
- 005
- 20170525102416.0
- 007
- ta
- 008
- 160408s2015 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1186/s13000-015-0280-6 $2 doi
- 024 7_
- $a 10.1186/s13000-015-0280-6 $2 doi
- 035 __
- $a (PubMed)25928282
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Héžová, Renata $u Molecular Oncology II - Solid Cancers, Molecular Medicine Central European Institute of Technology, Masaryk University, Brno, Czech Republic. renata.hezova@gmail.com. Department of Comprehensive Cancer Care, Masaryk Memorial Cancer Institute, Zluty kopec 7, Brno, 656 53, Czech Republic. renata.hezova@gmail.com. $7 xx0157096
- 245 10
- $a Diagnostic and prognostic potential of miR-21, miR-29c, miR-148 and miR-203 in adenocarcinoma and squamous cell carcinoma of esophagus / $c R. Hezova, A. Kovarikova, J. Srovnal, M. Zemanova, T. Harustiak, J. Ehrmann, M. Hajduch, M. Svoboda, M. Sachlova, O. Slaby,
- 520 9_
- $a BACKGROUND: Esophageal cancer is the malignant tumor with very poor prognosis and increasing incidence often diagnosed at very late stage, so the prognosis of affected patients is unsatisfactory, despite the development of therapeutic option such as surgery, chemotherapy and radiotherapy. Consequently, there is a great need for biomarkers to allow a tailored multimodality approach with increased efficiency. Altered expression of microRNAs has been reported in wide range of malignancies, including esophageal cancer. The aim of this study was to examine the expression levels of candidate microRNAs in esophageal cancer and evaluate their diagnostic and prognostic potential. FINDINGS: Using quantitative real-time PCR, expression levels of 9 candidate microRNAs were examined in 62 tissue samples, 23 esophageal adenocarcinomas, 22 esophageal squamous cell carcinomas and 17 adjacent esophageal mucosa samples. MicroRNA expression levels were further analyzed in regards to clinico-pathological features of esophageal cancer patients. We observed significantly decreased levels of miR-203 and increased levels of miR-21 in adenocarcinoma tissues when compared to normal mucosa. MiR-29c and miR-148 indicated good ability to distinguish between histological subtypes of esophageal cancer. MiR-203 and miR-148 were linked to disease-free survival and overall survival in esophageal adenocarcinoma patients, and miR-148 also in esophageal squamous cell carcinoma patients. CONCLUSIONS: Our data suggest that altered expression of miR-21, miR-29c, miR-148 and miR-203 are related to neoplastic transformation and progression of the disease and these microRNAs could serve as a potential diagnostic and prognostic biomarkers in esophageal cancer. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/4646922201567057.
- 650 _2
- $a adenokarcinom $x diagnóza $x genetika $7 D000230
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a nádorové biomarkery $x analýza $x genetika $x metabolismus $7 D014408
- 650 _2
- $a spinocelulární karcinom $x diagnóza $x genetika $7 D002294
- 650 _2
- $a nádory jícnu $x diagnóza $x genetika $7 D004938
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a regulace genové exprese u nádorů $x genetika $7 D015972
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a mikro RNA $x genetika $7 D035683
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a prognóza $7 D011379
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Kovaříková, Alena $u Molecular Oncology II - Solid Cancers, Molecular Medicine Central European Institute of Technology, Masaryk University, Brno, Czech Republic. aluskakovarikova@centrum.cz. $7 _AN065532
- 700 1_
- $a Srovnal, Josef $u Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University Olomouc, Olomouc, 779 00, Czech Republic. srovnalj@gmail.com. $7 xx0091239
- 700 1_
- $a Zemanová, Milada $u Department of Oncology, General University Hospital in Prague, Prague, Czech Republic. Milada.Zemanova@vfn.cz. $7 xx0060597
- 700 1_
- $a Haruštiak, Tomáš $u 3rd Department of Surgery, University Hospital in Motol, Prague, Czech Republic. TomasHarustiak@seznam.cz. $7 xx0096527
- 700 1_
- $a Ehrmann, Jiří, $u Department of Histology and Embryology, Faculty of Medicine and Dentistry, Palacky University and University Hospital, Olomouc, 779 00, Czech Republic. jiri.ehrmann@gmail.com. $d 1967- $7 jo2003163162
- 700 1_
- $a Hajdúch, Marián, $u Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University Olomouc, Olomouc, 779 00, Czech Republic. hajduchm@gmail.com. $d 1969- $7 xx0050218
- 700 1_
- $a Svoboda, Marek, $u Department of Comprehensive Cancer Care, Masaryk Memorial Cancer Institute, Zluty kopec 7, Brno, 656 53, Czech Republic. msvoboda@mou.cz. $d 1975- $7 xx0098478
- 700 1_
- $a Šachlová, Milana, $u Department of Comprehensive Cancer Care, Masaryk Memorial Cancer Institute, Zluty kopec 7, Brno, 656 53, Czech Republic. sachlova@mou.cz. $d 1959- $7 mzk2006322883
- 700 1_
- $a Slabý, Ondřej, $u Molecular Oncology II - Solid Cancers, Molecular Medicine Central European Institute of Technology, Masaryk University, Brno, Czech Republic. on.slaby@gmail.com. Department of Comprehensive Cancer Care, Masaryk Memorial Cancer Institute, Zluty kopec 7, Brno, 656 53, Czech Republic. on.slaby@gmail.com. $d 1981- $7 js20030220015
- 773 0_
- $w MED00165474 $t Diagnostic pathology $x 1746-1596 $g Roč. 10, č. - (2015), s. 42
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/25928282 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20160408 $b ABA008
- 991 __
- $a 20170525102814 $b ABA008
- 999 __
- $a ok $b bmc $g 1113676 $s 934615
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2015 $b 10 $c - $d 42 $e 20150428 $i 1746-1596 $m Diagnostic pathology $n Diagn Pathol $x MED00165474
- GRA __
- $a NT13585 $p MZ0
- LZP __
- $a Pubmed-20160408