Gao Jingfang, Arbman Gunnar, He Lujun, Qiao Fang, Zhang Zhiyong, Zhao Zengren, Rosell Johan, Sun Xiao-Feng
Department of Oncology, Institute of Biomedicine and Surgery, Linköping University, Linköping, Sweden.
Acta Oncol. 2008;47(3):372-8. doi: 10.1080/02841860701644052. Epub 2007 Sep 26.
beta-mannosidase, encoded by MANBA, has been suggested to be implicated in cancers, while genetic variations in the MANBA in relation to colorectal cancer (CRC) risk has not been examined. In this study, we investigated the relationship of a polymorphic CA repeat in MANBA gene with CRC risk in 152 Swedish CRC patients and 441 Swedish controls, and 196 Chinese CRC patients and 577 Chinese controls, as well as the clinicopathologic significance of this polymorphism on CRC patients, by using capillary electrophoresis. The MANBA genotypes were related to CRC risk in the Swedish population (p=0.03), but not in the Chinese population. In the Swedish population, individuals with < 22 CAs/< 22 CAs had significantly increased risk for CRC compared with those with >or=22 CAs/>or= 22 CAs (gender-age-adjusted analysis: OR 1.93, 95% CI 1.06-3.51). There was no relationship between the polymorphism and clinicopathologic variables. These findings suggest the different susceptibilities of this polymorphism to CRC development in the two populations.
由MANBA编码的β-甘露糖苷酶被认为与癌症有关,而MANBA基因的遗传变异与结直肠癌(CRC)风险的关系尚未得到研究。在本研究中,我们通过毛细管电泳研究了MANBA基因中一个多态性CA重复序列与152例瑞典CRC患者和441例瑞典对照、196例中国CRC患者和577例中国对照中CRC风险的关系,以及该多态性对CRC患者的临床病理意义。MANBA基因型与瑞典人群的CRC风险相关(p = 0.03),但与中国人群无关。在瑞典人群中,与具有≥22个CA/≥22个CA的个体相比,具有<22个CA/<22个CA的个体患CRC的风险显著增加(性别-年龄校正分析:OR 1.93,95%CI 1.06 - 3.51)。该多态性与临床病理变量之间没有关系。这些发现表明该多态性在两个人群中对CRC发生的易感性不同。