Investigation of FJ 194940.1 gene alternative splicing in colon cancer and its association with clinicopathological parameters

被引:3
作者
Bartczak-Tomczyk, Malwina [1 ]
Salagacka, Aleksandra [1 ]
Mirowski, Marek [1 ]
Balcerczak, Ewa [1 ]
机构
[1] Med Univ Lodz, Dept Pharmaceut Biochem, Lab Mol Biol & Pharmacogen, PL-90151 Lodz, Poland
关键词
FJ; 194940.1; expression; alternative splicing; transcript; colon cancer; PROSTATE-CANCER; EXPRESSION;
D O I
10.3892/etm.2011.378
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Colorectal cancer (CRC) is one of the most frequent neoplasms and is responsible for the second highest mortality rate of all cancers in the more developed regions of the world. The molecular mechanisms of CRC are relatively well characterized and are correlated to the accumulation of genetic mutations and certain patterns of gene expression/over-expression. There are a number of possible molecular factors involved in CRC progression in the aforementioned pathways, which are as yet not well described. One of these factors appears to be the gene FJ 194940.1, previously termed P65. FJ 194940.1 consists of 6 exons and probably undergoes alternative splicing in malignant tissues. In this study, tissue samples from 102 patients with colon cancer were investigated to confirm alternative splicing and to correlate results obtained with clinicopathological parameters. A total of 18 splice variants, which arise from various combinations of 4 exons (II, III, IV and V) and exon-exon junctions between exons 1 and 2 (I/II); 2 and 3 (II/III); 3 and 4 (III/IV), as well as 4 and 5 (IV/V), were found. For statistical analysis the full length transcript was divided into parts A and B. Part A consisted of exons II and Ill, as well as I/II and II/III exon-exon junctions, whereas part B comprised exons IV and V, as well as III/IV and IV/V exon-exon junctions. The expression of part B of the FJ 194940.1 gene transcript is correlated with welldifferentiated (G1) and moderately differentiated cases (G2). Lymphocytic tumor infiltration, a good prognostic factor in CRC, was significantly correlated to the presence of all elements in part A of the FJ 194940.1 gene transcript. Patients who had all elements in part A of the transcript survived for a shorter duration. Investigation of the El 194940.1 gene revealed that the gene had undergone alternative splicing. However, the role of its transcripts and potential proteins should be examined in detail.
引用
收藏
页码:237 / 242
页数:6
相关论文
共 17 条
[1]   Expression and prognostic value of CD44 standard and variant v3 and v6 isoforms in prostate cancer [J].
Aaltomaa, S ;
Lipponen, P ;
Ala-Opas, M ;
Kosma, VM .
EUROPEAN UROLOGY, 2001, 39 (02) :138-144
[2]  
Balcerczak E, 2007, Int J Biomed Sci, V3, P287
[3]  
Balcerczak E, 2002, NEOPLASMA, V49, P295
[4]   Expression of the p65 gene in patients with colorectal cancer:: comparison with some histological typing, grading and clinical staging [J].
Balcerczak, M ;
Balcerczak, E ;
Pasz-Walczak, G ;
Kordek, R ;
Mirowski, M .
EJSO, 2004, 30 (03) :266-270
[5]  
Baudry D, 2000, CLIN CANCER RES, V6, P3957
[6]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[7]  
Czyz W, 2003, FOLIA HISTOCHEM CYTO, V41, P91
[8]   WT1 SUPPRESSES SYNTHESIS OF THE EPIDERMAL GROWTH-FACTOR RECEPTOR AND INDUCES APOPTOSIS [J].
ENGLERT, C ;
HOU, X ;
MAHESWARAN, S ;
BENNETT, P ;
NGWU, C ;
RE, GG ;
GARVIN, AJ ;
ROSNER, MR ;
HABER, DA .
EMBO JOURNAL, 1995, 14 (19) :4662-4675
[9]  
Hewitt SM, 1996, ANTICANCER RES, V16, P621
[10]   Alternatively spliced MDM2 transcripts in human breast cancer in relation to tumor necrosis and lymph node involvement [J].
Hori, M ;
Shimazaki, J ;
Inagawa, S ;
Itabashi, M ;
Hori, M .
PATHOLOGY INTERNATIONAL, 2000, 50 (10) :786-792