KOČÍ, Lenka, Katarína CHLEBOVÁ, Martina HÝŽĎALOVÁ, Jiřina HOFMANOVÁ, Miroslav JÍRA, Petr KYSELA, Alois KOZUBÍK, Zdeněk KALA and Pavel KREJČÍ. Apoptosis inhibitor 5 (API-5; AAC-11; FIF) is upregulated in human carcinomas in vivo. Oncology Letters. Spandidos Publ., 2012, vol. 3, No 4, p. 913-916. ISSN 1792-1074. Available from: https://dx.doi.org/10.3892/ol.2012.593.
Other formats:   BibTeX LaTeX RIS
Basic information
Original name Apoptosis inhibitor 5 (API-5; AAC-11; FIF) is upregulated in human carcinomas in vivo
Authors KOČÍ, Lenka (203 Czech Republic, guarantor), Katarína CHLEBOVÁ (203 Czech Republic, belonging to the institution), Martina HÝŽĎALOVÁ (203 Czech Republic), Jiřina HOFMANOVÁ (203 Czech Republic, belonging to the institution), Miroslav JÍRA (203 Czech Republic, belonging to the institution), Petr KYSELA (203 Czech Republic, belonging to the institution), Alois KOZUBÍK (203 Czech Republic, belonging to the institution), Zdeněk KALA (203 Czech Republic, belonging to the institution) and Pavel KREJČÍ (203 Czech Republic, belonging to the institution).
Edition Oncology Letters, Spandidos Publ. 2012, 1792-1074.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30200 3.2 Clinical medicine
Country of publisher Greece
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 0.237
RIV identification code RIV/00216224:14110/12:00065918
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.3892/ol.2012.593
UT WoS 000301307600033
Keywords in English apoptosis inhibitor 5; anti-apoptosis clone 11;carcinoma; human; apoptosis; magnetic bead selection
Tags International impact, Reviewed
Changed by Changed by: Ing. Mgr. Věra Pospíšilíková, učo 9005. Changed: 29/4/2014 10:18.
Abstract
Apoptosis inhibitor 5 (API-5) is a 55 kDa nuclear protein with potent anti-apoptotic signaling in tumor cells in vitro. In this study, we analyzed the expression of the API-5 protein in vivo in a broad spectrum of human carcinomas, including those of the colon, lung, liver, kidney, pancreas, stomach and esophagus using tumor tissues obtained during tumor resection. The results showed significant upregulation of API-5 expression in biopsies of lung (23%, n=13) and colorectal tumors (33%, n=27) in comparison with biopsies from the adjacent normal tissue. Colon cancer biopsies were used to study the cell populations with an upregulated level of expression of API-5 more closely. Using a magnetic bead based selection for the epithelial cell marker EpCAM, we purified epithelial cells from the tumor and control tissues and analyzed these cells for API-5 expression by western immunoblotting. We observed that EpCAM-positive tumor cells expressed API-5 in all three colorectal cancer cases tested, in contrast to the control EpCAM-positive and EpCAM negative cells isolated from the control or tumor tissues. These data suggest that the expression of the API-5 protein is upregulated in tumor epithelial cells and may serve as a prognostic marker in colorectal cancer.
Links
GAP305/11/0752, research and development projectName: Molekulární základy FGFR3 signalingu v kostní dysplázii
Investor: Czech Science Foundation
GA301/09/0587, research and development projectName: Nové dráhy FGFR3 signalingu v achondroplázii
Investor: Czech Science Foundation, Novel pathway of FGFR3 signaling in achondroplasia
MSM0021622430, plan (intention)Name: Funkční a molekulární charakteristiky nádorových a normálních kmenových buněk - identifikace cílů pro nová terapeutika a terapeutické strategie
Investor: Ministry of Education, Youth and Sports of the CR, Functional and molecular characteristics of cancer and normal stem cells - identification of targets for novel therapeutics and therapeutic strategies
2B06060, research and development projectName: Zefektivnění diagnostiky a léčby gastroezofageální refluxní choroby jícnu (Acronym: NPVII11002)
Investor: Ministry of Education, Youth and Sports of the CR
PrintDisplayed: 20/7/2024 00:28