Karlsen F, Rabbitts P H, Sundresan V, Hagmar B
Department of Pathology, Norwegian Radium Hospital, Montebello, Oslo.
Int J Cancer. 1994 Sep 15;58(6):787-92. doi: 10.1002/ijc.2910580606.
Loss of heterozygosity (LOH) has been extensively studied on the short arm of chromosome 3, and functional proofs have been obtained defining a tumor-suppressor locus at 3p21-22. We examined 31 paraffin-embedded cervical cancer samples for LOH, using 5 PCR-primer pairs, located around 3p21. Allele loss was found in 19 out of the 27 informative samples (70%) while 13 out of 23 informative samples (56%) had LOH located at 3p21-22. More of the human papillomavirus (HPV)-positive samples had LOH compared to the HPV-negative samples, giving only a weak association between loss of allele and HPV integration. Modifications of the DNA in the formaldehyde-fixed samples were detected, and further studies will be required to clarify how such artifacts may affect restriction fragment length polymorphism (RFLP) studies on fixed tissues.
杂合性缺失(LOH)已在3号染色体短臂上进行了广泛研究,并已获得功能证据,确定了3p21-22处的一个肿瘤抑制基因座。我们使用位于3p21周围的5对PCR引物,检测了31份石蜡包埋的宫颈癌样本中的LOH。在27份信息性样本中的19份(70%)中发现了等位基因缺失,而在23份信息性样本中的13份(56%)中,LOH位于3p21-22。与HPV阴性样本相比,更多的人乳头瘤病毒(HPV)阳性样本存在LOH,等位基因缺失与HPV整合之间的关联较弱。在甲醛固定样本中检测到了DNA修饰,需要进一步研究以阐明此类假象如何影响对固定组织的限制性片段长度多态性(RFLP)研究。