Department of Oncology, Changhai Hospital, the Second Military Medical University, Shanghai, China.
Key Laboratory of Systems Biology, State Key Laboratory of Cell Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
Oncogene. 2015 Oct 1;34(40):5198-205. doi: 10.1038/onc.2014.443. Epub 2015 Jan 26.
Certain predisposition factors such as BRCA1/2 and CHEK2 mutations cause familial breast cancers that occur early. In China, breast cancers are diagnosed at relatively younger age, and higher percentage of patients are diagnosed before 40 years, than that in Caucasians. However, the prevalence for BRCA1/2 mutations and reported CHEK2 germline mutations is much lower or absent in Chinese population, arguing for the need to study other novel risk alleles among Chinese breast cancer patients. In this study, we searched for CHEK2 mutations in young, high-risk breast cancer patients in China and detected a missense variant Y390C (1169A > G) in 12 of 150 patients (8.0%) and 2 in 250 healthy controls (0.8%, P = 0.0002). Four of the Y390C carriers have family history of breast and/or ovarian cancer. In patients without family history, Y390C carriers tend to develop breast cancer early, before 35 years of age. The codon change at Y390, a highly conserved residue located in CHEK2's kinase domain, appeared to significantly impair CHEK2 activity. Functional analysis suggested that the CHEK2 Y390C mutation is deleterious as judged by the mutant protein's inability to inactivate CDC25A or to activate p53 after DNA damage. Cells expressing the CHEK2 Y390C variant showed impaired p21 and Puma expression after DNA damage, and the deregulated cell cycle checkpoint and apoptotic response may help conserve mutations and therefore contribute to tumorigeneisis. Taken together, our results not only identified a novel CHEK2 allele that is associated with cancer families and confers increased breast cancer risk, but also showed that this allele significantly impairs CHEK2 function during DNA damage response. Our results provide further insight on how the function of such an important cancer gene may be impaired by existing mutations to facilitate tumorigenesis. It also offers a new subject for breast cancer monitoring, prevention and management.
某些易感因素,如 BRCA1/2 和 CHEK2 突变,会导致早发性家族性乳腺癌。在中国,乳腺癌的发病年龄相对较早,且 40 岁以下患者的比例高于白种人。然而,BRCA1/2 突变的发生率以及报道的 CHEK2 种系突变在中国人群中要低得多或不存在,这表明有必要在中国乳腺癌患者中研究其他新的风险等位基因。在这项研究中,我们在中国年轻的高危乳腺癌患者中寻找 CHEK2 突变,并在 150 名患者中的 12 名(8.0%)和 250 名健康对照中的 2 名(0.8%)中检测到错义变异 Y390C(1169A > G)(P = 0.0002)。携带 Y390C 的患者中有 4 人有乳腺癌和/或卵巢癌家族史。在无家族史的患者中,Y390C 携带者倾向于在 35 岁之前更早地患上乳腺癌。Y390 处的密码子变化,位于 CHEK2 激酶结构域中的一个高度保守残基,似乎显著削弱了 CHEK2 的活性。功能分析表明,根据突变蛋白无法使 CDC25A 失活或在 DNA 损伤后激活 p53,判断 CHEK2 Y390C 突变是有害的。表达 CHEK2 Y390C 变体的细胞在 DNA 损伤后显示出 p21 和 Puma 表达受损,失调的细胞周期检查点和凋亡反应可能有助于保存突变,从而促进肿瘤发生。总之,我们的研究结果不仅鉴定了一个与癌症家族相关并增加乳腺癌风险的新型 CHEK2 等位基因,还表明该等位基因在 DNA 损伤反应中显著削弱了 CHEK2 的功能。我们的研究结果进一步深入了解了重要癌症基因的功能如何因现有突变而受损,从而促进肿瘤发生。这也为乳腺癌监测、预防和管理提供了一个新的研究课题。