Pylkkänen Lea, Wolff Henrik, Stjernvall Tuula, Knuuttila Aija, Anttila Sisko, Husgafvel-Pursiainen Kirsti
Department of Industrial Hygiene and Toxicology, Finnish Institute of Occupational Health, Helsinki, Finland.
Virchows Arch. 2004 Jan;444(1):43-8. doi: 10.1007/s00428-003-0902-3. Epub 2003 Oct 16.
Human malignant mesothelioma (MM) is an aggressive neoplasm related to occupational exposure to asbestos and characterised by a long latency time. Multiple chromosomal deletions and DNA losses have been revealed in MM by studies performed with karyotypic, comparative genomic hybridisation and loss of heterozygosity (LOH) analyses. Among frequently deleted chromosomal sites, LOH at chromosome 3p has been detected in MM, suggesting the presence of one or several tumour suppressor genes that have an important role in development of the disease. The FHIT (fragile histidine triad) tumour suppressor gene, located at 3p14.2, has been proposed to be a target to major human lung carcinogens, such as tobacco smoke and asbestos. Although many studies have indicated decreased Fhit protein expression in a variety of malignancies, there is no report of FHIT gene aberrations or Fhit protein abnormalities in MM. We examined expression of the Fhit protein and LOH at the FHIT gene in malignant mesothelioma. Altogether, 13 paraffin embedded MM tumours were analysed for Fhit protein expression, and 21 fresh tumours and 10 cell cultures for LOH at the FHIT gene with two intragenic microsatellite markers. All tumours showed less intense immunostaining than normal bronchial epithelium or mesothelium. Fhit expression was absent or reduced in 54% (7 of 13) of the tumours, with the weakest staining observed in poorly differentiated areas. Allele loss was seen in 3 of 10 (30%) of the MM cell lines, but only in 1 of the 21 fresh tumours studied, suggesting concealment of LOH by normal cells present in MM tumours. In conclusion, our present data indicate a frequent decrease of Fhit protein expression, thus supporting the significance of FHIT inactivation in development of MM.
人类恶性间皮瘤(MM)是一种侵袭性肿瘤,与职业性接触石棉有关,其特征是潜伏期长。通过核型分析、比较基因组杂交和杂合性缺失(LOH)分析等研究发现,MM中存在多个染色体缺失和DNA丢失。在常见的染色体缺失位点中,MM中检测到3号染色体短臂(3p)的LOH,提示存在一个或几个在该疾病发生中起重要作用的肿瘤抑制基因。位于3p14.2的FHIT(脆性组氨酸三联体)肿瘤抑制基因被认为是主要人类肺癌致癌物(如烟草烟雾和石棉)的作用靶点。尽管许多研究表明多种恶性肿瘤中Fhit蛋白表达降低,但尚无关于MM中FHIT基因畸变或Fhit蛋白异常的报道。我们检测了恶性间皮瘤中Fhit蛋白的表达以及FHIT基因的LOH情况。总共对13个石蜡包埋的MM肿瘤进行了Fhit蛋白表达分析,对21个新鲜肿瘤和10个细胞培养物用两个基因内微卫星标记检测了FHIT基因的LOH。所有肿瘤的免疫染色强度均低于正常支气管上皮或间皮。54%(13个中的7个)的肿瘤Fhit表达缺失或降低,在低分化区域观察到最弱的染色。在10个MM细胞系中有3个(30%)出现等位基因缺失,但在21个研究的新鲜肿瘤中仅1个出现,提示MM肿瘤中存在的正常细胞掩盖了LOH。总之,我们目前的数据表明Fhit蛋白表达经常降低,从而支持FHIT失活在MM发生中的重要性。