Association between mutations in the CARD15/NOD2 gene and colorectal cancer in a Greek population
✍ Scribed by Ioannis Papaconstantinou; George Theodoropoulos; Maria Gazouli; Dimitris Panoussopoulos; Gerassimos J. Mantzaris; Evangelos Felekouras; John Bramis
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- French
- Weight
- 69 KB
- Volume
- 114
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Epidemiological observations suggest that cancer arises from chronically inflamed tissues. Inflammatory bowel disease (IBD) is a typical example since patients with longstanding IBD are at increased risk for development of colorectal cancer (CRC). Therefore, genetic factors predisposing to or implicated in the chronic inflammatory process in IBD may simultaneously predispose to CRC. Recently CARD15/NOD2 has been associated with IBD, which further strengthens the notion that the inflammatory response plays a crucial role in this disease. Several mutations have been identified in the CARD15/NOD2 gene, which appear with significantly higher frequency in patients with IBD. In this report, we have examined the frequency of the 3 major mutations R702W, G908R and 3020insC of the CARD2/NOD2 gene in a series of 104 consecutive Greek patients with sporadic colorectal cancer and 100 healthy individuals. The frequency of all the mutations was significantly elevated compared to the control population (R702W, OR=5.00, p=0.023; G908R, OR=2.78, p=0.025; 3020insC, OR=2.44, p=0.017). Patients with advanced stage tumors were more frequently carriers of at least 1 variant in the CARD15/NOD2 gene (p=0.009). Our results suggest that CARD2/NOD2 may be a genetic factor that predispose to sporadic colorectal cancer. © 2005 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
## Abstract __MKK4__ (mitogen‐activated protein kinase kinase 4, NM\_003010.2), which belongs to the mitogen‐activated protein kinase pathways, possesses functions in tumorigenesis. We hypothesized the genetic variants in __MKK4__ gene may alter its functions and thus cancer risk. In current hospit
## Conclusions: TLR 4 A299G appears to be a significant risk factor for CD, in particular colonic, nonstricturing disease. Furthermore, we identified a novel NOD2 haplotype that strengthens the relationship between TLR4 A299G and these phenotypes.
## Abstract GST Alpha 4 (GSTA4) has an important role in the protection against oxidative stress induced by carcinogens such as tobacco smoke. However, few studies investigated the association between __GSTA4__ polymorphisms and lung cancer risk. We genotyped three selected __GSTA4__ SNPs (rs182623
Defects of neural tube closure are among the most common of all human malformations. Epidemiological and genetic studies indicate that most of these defects are multifactorial in origin with genetic and environmental causes. Although periconceptional supplementation of the maternal diet with folic a
## Abstract Aurora‐A kinase is considered a potential cancer susceptibility gene that encodes a centrosome‐associated, cell cycle‐regulated serine/threonine kinase. We studied two single nucleotide polymorphisms (SNP) in the coding region of Aurora‐A, 91T‐to‐A (F31I) and 169G‐to‐A (V57I). We studie