Chirila D N, Popp R A, Balacescu O, Turdeanu N A, Constantea N A, Pop T R, Vesa S C, Ciuce C
Iuliu Haåieganu University of Medicine and Pharmacy, Vth Surgical Department, Cluj-Napoca, Romania.
Chirurgia (Bucur). 2013 May-Jun;108(3):365-71.
the present study evaluates genetic polymorphisms of three glutathione S-transferases (GSTM1, GSTT1and GSTP1) in patients with synchronous malignant colorectal tumors and the association of synchronous colorectal cancers with other cancers.
from 420 patients with a colorectal cancer admitted to our hospital between 2005-2012, we selected for genetic analysis 20 patients with multiple synchronous malignant colorectal tumors and 9 patients with asynchronous association of colorectal cancer with another cancer. We searched for GST genotypes, comparing the results with controls.
the genetic analysis was possible only in 19 patients with colorectal synchronous cancers and 9 patients with asynchronous association of colorectal cancer with another cancer; we found a statistically significant difference for null GSTM1 genotype frequency between these patients and the control group; we found no differences regarding the frequency of null GSTT1 genotype and Ile105Val polymorphism of GSTP1 in patients with synchronous cancers compared with the control group.
in our study we found the null GSTM1 genotype as a risk factor for multiple colorectal synchronous cancers and for an association of synchronous colorectal with other cancers
本研究评估同步性恶性结直肠肿瘤患者中三种谷胱甘肽S-转移酶(GSTM1、GSTT1和GSTP1)的基因多态性,以及同步性结直肠癌与其他癌症的关联。
从2005年至2012年入住我院的420例结直肠癌患者中,我们选择了20例患有多个同步性恶性结直肠肿瘤的患者和9例结直肠癌与另一种癌症存在异步关联的患者进行基因分析。我们检测了GST基因型,并将结果与对照组进行比较。
仅对19例结直肠同步癌患者和9例结直肠癌与另一种癌症存在异步关联的患者进行了基因分析;我们发现这些患者与对照组之间,无效GSTM1基因型频率存在统计学显著差异;与对照组相比,同步癌患者中无效GSTT1基因型频率和GSTP1的Ile105Val多态性频率无差异。
在我们的研究中,我们发现无效GSTM1基因型是多个结直肠同步癌以及同步性结直肠癌与其他癌症关联的一个危险因素。