Gallmeier Eike, Kern Scott E
Department of Oncology, The Sol Goldman Pancreatic Cancer Research Center, Baltimore, Maryland, USA.
Cancer Biol Ther. 2005 Jul;4(7):703-6. doi: 10.4161/cbt.4.7.1909. Epub 2005 Jul 10.
The specific killing of cells impaired in BRCA2 function upon treatment with poly (ADP-ribose) polymerase (PARP) inhibitors has recently been reported by two groups. CAPAN1, which was not characterized in these reports, represents the only human cancer cell line harboring the frequent, naturally occurring BRCA2 6174delT frameshift mutation accompanied by loss of the second allele. The severe impact of this mutation on BRCA2 function has been extensively characterized. However, PARP inhibition by 3-aminobenzamide or NU1025 did not result in significant cell death in CAPAN1 cells. Our data raise concern about the uniformity of the specific cell killing of BRCA2-deficient cells upon PARP inhibition and therefore urge caution as to whether prior findings are fully generalizable for the specific treatment of human cancers harboring naturally occurring, inactivating forms of BRCA2 mutations.
最近有两个研究小组报告称,在用聚(ADP - 核糖)聚合酶(PARP)抑制剂治疗后,BRCA2功能受损的细胞会被特异性杀伤。CAPAN1细胞系在这些报告中未被研究,它是唯一一种携带常见的、自然发生的BRCA2 6174delT移码突变且伴有第二个等位基因缺失的人类癌细胞系。这种突变对BRCA2功能的严重影响已得到广泛研究。然而,3 - 氨基苯甲酰胺或NU1025对PARP的抑制作用并未导致CAPAN1细胞出现明显的细胞死亡。我们的数据引发了人们对PARP抑制后BRCA2缺陷细胞特异性杀伤的一致性的关注,因此对于先前的研究结果是否完全适用于携带自然发生的、失活形式BRCA2突变的人类癌症的特异性治疗,我们需谨慎对待。