Schayek Hagit, Laitman Yael, Katz Lior H, Pras Elon, Ries-Levavi Liat, Barak Frida, Friedman Eitan
Gertner Oncogenetics Unit, Sheba Medical Center, Tel Hashomer, Israel.
Institute of Gastroenterology, Sheba Medical Center, Tel Hashomer, Israel.
Isr Med Assoc J. 2017 Jun;19(6):365-367.
Biallelic BLM gene mutation carriers are at an increased risk for cancer, including colorectal cancer (CRC). Whether heterozygous BLM gene mutations confer an increased cancer risk remains controversial.
To evaluate CRC and endometrial cancer risk in BLM heterozygous mutation carriers.
Jewish Ashkenazim at high risk for colon or endometrial cancer and endometrial cancer cases unselected for family history were genotyped for the BLMAsh predominant mutation.
Overall, 243 high-risk individuals were included: 97 men CRC patients (55.12 ± 12.3 years at diagnosis), 109 women with CRC (56.5 ± 13.7 years), 32 women with endometrial cancer (58.25 ± 13.4 years) and 5 women with both CRC and endometrial cancer. In addition, 120 unselected Ashkenazi women with endometrial cancer (64.2 ± 11.58 years) were genotyped. The BLMAsh mutation was present in 4/243 (1.65%) high-risk patients; 2 CRC (0.97%) 2 endometrial cancer (5.4%), and 1/120 unselected endometrial cancer patients (0.84%). Notably, in high-risk cases, BLMAsh mutation carriers were diagnosed at a younger age (for CRC 47.5 ± 7.8 years; P = 0.32 ; endometrial cancer 49.5 ± 7.7 years; P = 0.36) compared with non-carriers.
Ashkenazi high risk CRC/endometrial cancer, and women with endometrial cancer have a higher rate of BLMAsh heterozygous mutation compared with the general population. BLMAsh heterozygous mutation carriers are diagnosed with CRC and endometrial cancer at a younger age compared with non-carriers. These observations should be validated and the possible clinical implications assessed.
双等位基因BLM基因突变携带者患癌风险增加,包括结直肠癌(CRC)。杂合性BLM基因突变是否会增加癌症风险仍存在争议。
评估BLM杂合突变携带者患结直肠癌和子宫内膜癌的风险。
对患结肠癌或子宫内膜癌风险高的犹太裔阿什肯纳兹人以及未根据家族史选择的子宫内膜癌病例进行BLMAsh主要突变的基因分型。
总共纳入了243名高危个体:97名男性CRC患者(诊断时年龄为55.12±12.3岁),109名女性CRC患者(56.5±13.7岁),32名子宫内膜癌女性患者(58.25±13.4岁)以及5名同时患有CRC和子宫内膜癌的女性。此外,对120名未根据家族史选择的阿什肯纳兹子宫内膜癌女性患者(64.2±11.58岁)进行了基因分型。BLMAsh突变存在于4/243(1.65%)的高危患者中;2例CRC(0.97%),2例子宫内膜癌(5.4%),以及1/120名未根据家族史选择的子宫内膜癌患者(0.84%)。值得注意的是,在高危病例中,与非携带者相比,BLMAsh突变携带者被诊断出的年龄更小(CRC为47.5±7.8岁;P = 0.32;子宫内膜癌为49.5±7.7岁;P = 0.36)。
与一般人群相比,阿什肯纳兹高危CRC/子宫内膜癌患者以及子宫内膜癌女性患者中BLMAsh杂合突变率更高。与非携带者相比,BLMAsh杂合突变携带者被诊断出患CRC和子宫内膜癌的年龄更小。这些观察结果应得到验证,并评估其可能的临床意义。