Laboratory of Venoms and Therapeutic Biomolecules, LR16IPT08 Institute Pasteur of Tunis, University of Tunis El Manar, 13 Place Pasteur, BP74, 1002, Tunis, Belvédère, Tunisia.
Center for Biomedical Informatics, School of Medicine, University of Missouri, Columbia, MO, USA.
BMC Cancer. 2020 Nov 10;20(1):1086. doi: 10.1186/s12885-020-07605-7.
Colorectal cancer (CRC) is the third most diagnosed malignancy worldwide. The global burden is expected to increase along with ongoing westernized behaviors and lifestyle. The etiology of CRC remains elusive and most likely combines environmental and genetic factors. The Kv2.1 potassium channel encoded by KCNB1 plays a collection of roles in malignancy of cancer and may be a key factor of CRC susceptibility. Our study provides baseline association between Tunisian CRC and interactions between KCNB1 variants and lifestyle factors.
A case-control study involving 300 CRC patients, and 300 controls was conducted Patients were carefully phenotyped and followed till the end of study. KCNB1 genotyping was confirmed by Sanger sequencing. Bivariate and multivariable logistic regression analyses were used to assess the clinical status, lifestyle and study polymorphisms association with CRC.
We noted significant gender association with CRC occurrence. Moreover, CRC risk increases with high meat and fat consumption, alcohol use and physical activity (PA). Carriage of rs1051296 A/G and both rs11468831 ins/del and del/del genotypes (p < 0.001) were significantly associated with CRC risk. Analysis according to gender reveals correlation of rs1051295 A/G, rs11468831 non ins/ins (p = 0.01) with CRC susceptibility regardless of patients' gender while rs3331 T/C (p = 0.012) was associated with females. Stratification study according to malignancy site; Rectal Cancer (RC) and Colon Cancer (CC), reveals increasing RC risk by gender and high meat and fat consumption, alcohol use and PA. However, additional association with high brine consumption was noted for CC. The rs1051295 A/G (p = 0.01) was associated with RC risk. Increased CC risk was associated with carriage of rs1051295 A/G, rs11168831 (del/del) and (ins/del) genotypes.
The risk of CRC increases with modifiable factors by Western influences on Tunisian lifestyle such as alcohol use, high fat consumption and possibly inadequate intake of vegetables. In addition, KCNB1 polymorphisms also markedly influence CRC susceptibility. Our study establishes key elements of a baseline characterization of clinical state, Western influenced lifestyle and KCNB1 variants associated with Tunisian CRC.
结直肠癌(CRC)是全球第三大常见恶性肿瘤。随着西方化行为和生活方式的持续,预计全球负担将增加。CRC 的病因仍然难以捉摸,最有可能是环境和遗传因素的结合。由 KCNB1 编码的 Kv2.1 钾通道在癌症恶性肿瘤中发挥着一系列作用,可能是 CRC 易感性的关键因素。我们的研究提供了突尼斯 CRC 与 KCNB1 变体和生活方式因素之间相互作用的基线关联。
我们进行了一项病例对照研究,涉及 300 名 CRC 患者和 300 名对照。对患者进行了仔细的表型分析,并随访至研究结束。通过 Sanger 测序证实 KCNB1 基因分型。使用双变量和多变量逻辑回归分析评估临床状况、生活方式和研究多态性与 CRC 的关联。
我们注意到 CRC 发生与性别存在显著关联。此外,高肉类和脂肪摄入、饮酒和体力活动(PA)会增加 CRC 风险。携带 rs1051296 A/G 以及 rs11468831 ins/del 和 del/del 基因型(p<0.001)与 CRC 风险显著相关。根据性别进行的分析显示,rs1051295 A/G、rs11468831 非 ins/ins(p=0.01)与 CRC 易感性相关,无论患者性别如何,而 rs3331 T/C(p=0.012)与女性相关。根据恶性肿瘤部位进行分层研究;直肠癌(RC)和结肠癌(CC)显示,RC 风险因性别和高肉类和脂肪摄入、饮酒和 PA 而增加。然而,还发现 CC 与高盐水摄入有关。rs1051295 A/G(p=0.01)与 RC 风险相关。携带 rs1051295 A/G、rs11168831(del/del)和(ins/del)基因型的 CC 风险增加。
CRC 风险随着西方化生活方式对突尼斯的影响而增加,例如饮酒、高脂肪摄入和蔬菜摄入不足等可改变的因素。此外,KCNB1 多态性也显著影响 CRC 的易感性。我们的研究建立了突尼斯 CRC 与临床状态、受西方影响的生活方式和 KCNB1 变体相关的基线特征的关键要素。