Membrane-associated phospholipase A1 beta (LIPI) is an Ewing tumour-associated cancer/testis antigen

被引:34
作者
Foell, Juergen L. [1 ]
Hesse, Manuela [1 ]
Volkmer, Ines [1 ]
Schmiedel, Benjamin J. [1 ]
Neumann, Ingo [1 ]
Staege, Martin S. [1 ]
机构
[1] Univ Halle Wittenberg, Childrens Canc Res Ctr, Dept Paediat, D-06097 Halle, Germany
关键词
cancer testis antigens; Ewing family tumours; LIPI; polymerase chain reaction;
D O I
10.1002/pbc.21602
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Cancer/testis antigens (CTA) represent a heterogeneous group of antigens expressed nearly exclusively in tumour cells and testis. Recently, we identified phospholipase At beta (a CTA also known as lipase member 1, LIPI) as a gene with high expression in Ewing family tumours (EFT). In the present paper we analyzed expression of LIPI in a panel of normal tissues and tumour samples. Procedure. The expression of CTA in EFT and normal tissues was analyzed by using DNA microarray datasets. Expression of LIPI in EFT, a panel of other tumour samples, and normal tissues was analyzed by using RT-PCR and quantitative RT-PCR. Results. LIPI was expressed in EFT samples but not in other investigated tumour samples. Expression of LIPI in normal tissues was restricted to testis and thyroid. However, expression in these tissues was low compared with EFT. Interestingly testis as well as thyroid expressed all analyzed EFT-associated transcripts, suggesting that these tissues harbour a small cell population with molecular features of EFT. The sensitivity of the LIPI RT-PCR was similar to the sensitivity of the conventional EWSR1-FLI1 RT-PCR, suggesting that LIPI might be useful as additional diagnostic target structure. Conclusions. The human cancer/testis antigen LIPI is highly expressed in Ewing family tumours and can be easily detected by RT-PCR or quantitative RT-PCR. LIPI might be an interesting target for the development of future diagnostic tools or treatment strategies.
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页码:228 / 234
页数:7
相关论文
共 29 条
[1]   Cancer-testis antigens are commonly expressed in multiple myeloma and induce systemic immunity following allogeneic stem cell transplantation [J].
Atanackovic, Djordje ;
Arfsten, Julia ;
Cao, Yanran ;
Gnjatic, Sacha ;
Schnieders, Frank ;
Bartels, Katrin ;
Schilling, Georgia ;
Faltz, Christiane ;
Wolschke, Christine ;
Dierlamm, Judith ;
Ritter, Gerd ;
Eiermann, Thomas ;
Hossfeld, Dieter Kurt ;
Zander, Axel R. ;
Jungbluth, Achim A. ;
Old, Lloyd J. ;
Bokemeyer, Carsten ;
Kroeger, Nicolaus .
BLOOD, 2007, 109 (03) :1103-1112
[2]   Melanoma genetics and the development of rational therapeutics [J].
Chudnovsky, Y ;
Khavari, PA ;
Adams, AE .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (04) :813-824
[3]   Molecular confirmation of Ewing sarcoma [J].
Dagher, R ;
Pham, TA ;
Sorbara, L ;
Kumar, S ;
Long, L ;
Bernstein, D ;
Mackall, C ;
Raffeld, M ;
Tsokos, M ;
Helman, L .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2001, 23 (04) :221-224
[4]   Human ES cell-derived neural rosettes reveal a functionally distinct early neural stem cell stage [J].
Elkabetz, Yechiel ;
Panagiotakos, Georgia ;
Al Shamy, George ;
Socci, Nicholas D. ;
Tabar, Viviane ;
Studer, Lorenz .
GENES & DEVELOPMENT, 2008, 22 (02) :152-165
[5]   A PCR-based expression signature of malignancy in follicular thyroid tumors [J].
Foukakis, Theodoros ;
Gusnanto, Arief ;
Au, Amy Y. M. ;
Hoog, Anders ;
Lui, Weng-Onn ;
Larsson, Catharina ;
Wallin, Goran ;
Zedenius, Jan .
ENDOCRINE-RELATED CANCER, 2007, 14 (02) :381-391
[6]   Interpreting expression profiles of cancers by genome-wide survey of breadth of expression in normal tissues [J].
Ge, XJ ;
Yamamoto, S ;
Tsutsumi, S ;
Midorikawa, Y ;
Ihara, S ;
Wang, SM ;
Aburatani, H .
GENOMICS, 2005, 86 (02) :127-141
[7]  
Hellgren I, 2000, BIOL PHARM BULL, V23, P700
[8]   Biochemical and molecular characterization of two phosphatidic acid-selective phospholipase A1s, mPA-PLA1α and mPA-PLA1β [J].
Hiramatsu, T ;
Sonoda, H ;
Takanezawa, Y ;
Morikawa, R ;
Ishida, M ;
Kasahara, K ;
Sanai, Y ;
Taguchi, R ;
Aoki, J ;
Arai, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (49) :49438-49447
[9]   Cancer-germline gene expression in pediatric solid tumors using quantitative real-time PCR [J].
Jacobs, Joannes F. M. ;
Brasseur, Francis ;
Hulsbergen-van de Kaa, Christina A. ;
van de Rakt, Mandy W. M. M. ;
Figdor, Carl G. ;
Adema, Gosse J. ;
Hoogerbrugge, Peter M. ;
Coulie, Pierre G. ;
de Vries, I. Jolanda M. .
INTERNATIONAL JOURNAL OF CANCER, 2007, 120 (01) :67-74
[10]   Expression profiles provide insights into early malignant potential and skeletal abnormalities in multiple endocrine neoplasia type 2B syndrome tumors [J].
Jain, SJ ;
Watson, MA ;
DeBenedetti, MK ;
Hiraki, Y ;
Moley, JF ;
Milbrandt, J .
CANCER RESEARCH, 2004, 64 (11) :3907-3913