Chang Zhengqi, Song Ruoxian, Xu Songfeng, Xu Ming, Yu Xiuchun
Department of Orthopedics, General Hospital of Jinan Military Commanding Region, Jinan, 250031, Shandong Province, China.
Tumour Biol. 2014 Jul;35(7):6809-14. doi: 10.1007/s13277-014-1891-3. Epub 2014 Apr 12.
Osteosarcoma has become a health threat for adolescents and young adults. To identify the genetic risk factor for the malignancy is in urgent need. Several studies have investigated the role of CD 152 polymorphisms in osteosarcoma in a sample of Chinese population. However, the association is poorly defined due to lack of a sufficiently large sample. In this study, we performed a meta-analysis of all CD 152 polymorphisms that had been implicated in osteosarcoma to examine the association. We searched the electronic MEDLINE database until December 31, 2013, to identify the studies regarding the association between CD 152 polymorphisms and osteosarcoma. Inclusion criteria were followed in the selection of eligible study. The genotypic and allelic data were collected from all studies included to evaluate the risk of osteosarcoma (odds ratio, OR). We found statistically significant evidence of the studied CD 152 polymorphisms and increased risk of osteosarcoma in homozygous (OR = 1.79, 95 % CI = 1.40-2.29, P = 0.958), recessive (OR = 1.77, 95 % CI = 1.40-2.25, P = 0.899), and allele model (OR = 1.21, 95 % CI = 1.09-1.34, P = 1.000). This increased risk was also revealed in single nucleotide polymorphism (SNP) +49G>A and SNP 326G>A. Our meta-analysis indicates that there may be an association between CD 152 polymorphisms and risk of osteosarcoma in Chinese population. Further validation of the observation is necessary.
骨肉瘤已成为青少年和青年的健康威胁。迫切需要确定这种恶性肿瘤的遗传风险因素。几项研究在中国人群样本中调查了CD 152多态性在骨肉瘤中的作用。然而,由于缺乏足够大的样本,这种关联尚未明确界定。在本研究中,我们对所有与骨肉瘤相关的CD 152多态性进行了荟萃分析,以检验这种关联。我们检索了截至2013年12月31日的电子MEDLINE数据库,以确定有关CD 152多态性与骨肉瘤之间关联的研究。在选择合格研究时遵循纳入标准。从所有纳入研究中收集基因型和等位基因数据,以评估骨肉瘤风险(比值比,OR)。我们发现,在所研究的CD 152多态性与纯合子(OR = 1.79,95%可信区间 = 1.40 - 2.29,P = 0.958)、隐性(OR = 1.77,95%可信区间 = 1.40 - 2.25,P = 0.899)和等位基因模型(OR = 1.21,95%可信区间 = 1.09 - 1.34,P = 1.000)中骨肉瘤风险增加之间存在统计学显著证据。单核苷酸多态性(SNP)+49G>A和SNP 326G>A中也显示出这种风险增加。我们的荟萃分析表明,中国人群中CD 152多态性与骨肉瘤风险之间可能存在关联。有必要对这一观察结果进行进一步验证。