Hecht F, Sutherland G R
Cancer Genet Cytogenet. 1984 Jun;12(2):179-81. doi: 10.1016/0165-4608(84)90132-8.
To determine whether there might be a statistically significant association between fragile sites and cancer breakpoints, we examined the locations of the 21 fragile sites and the 50 cancer breakpoints recently accepted by the Seventh Human Gene Mapping Workshop. Nine of the 21 fragile sites appeared to be located at or near a cancer breakpoint. The chi-square test for association gives a value of 15.8 (p less than 0.001) indicating that there is a very highly significant statistical association between human fragile sites and cancer breakpoints. This association is not narrowly limited to one class of fragile site, such as those sensitive to folate or to one type of cancer, but appears to extend to leukemia, lymphoma, and solid cancer. To more fully understand the meaning of this intriguing association between fragile sites and cancer breakpoints, future research will need to locate additional fragile sites and cancer breakpoints with precision, record their concurrence in individuals and families, determine if fragile site families are predisposed to cancer, and prove that a fragile site and a cancer breakpoint that appear to be coincident are at the same point on the DNA level.
为了确定脆性位点与癌症断点之间是否可能存在统计学上的显著关联,我们研究了21个脆性位点以及最近被第七届人类基因定位研讨会认可的50个癌症断点的位置。21个脆性位点中有9个似乎位于癌症断点处或其附近。关联性的卡方检验得出的值为15.8(p小于0.001),这表明人类脆性位点与癌症断点之间存在非常高度显著的统计学关联。这种关联并不局限于某一类脆性位点,比如对叶酸敏感的那些脆性位点,也不局限于某一种癌症类型,而是似乎延伸到了白血病、淋巴瘤和实体癌。为了更全面地理解脆性位点与癌症断点之间这种有趣关联的意义,未来的研究需要精确地定位更多的脆性位点和癌症断点,记录它们在个体和家族中的同时出现情况,确定携带脆性位点的家族是否易患癌症,并证明看似重合的一个脆性位点和一个癌症断点在DNA水平上处于同一点。