Campanella Nathália C, Penna Valter, Abrahão-Machado Lucas Faria, Cruvinel-Carloni Adriana, Ribeiro Guilherme, Soares Paula, Scapulatempo-Neto Cristovam, Reis Rui M
Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, São Paulo - Brazil.
Department of Orthopedy, Barretos Cancer Hospital, Barretos, São Paulo - Brazil.
Int J Biol Markers. 2016 Feb 28;31(1):e62-7. doi: 10.5301/jbm.5000168.
Oncogenic hotspot mutations in the promoter region of the TERT gene have been identified in several cancer types as being associated with a worse outcome. Additionally, a polymorphism (rs2853669) in the TERT promoter region was reported to modify the survival of TERT-mutated patients. Our aim is to determine the frequency of c.-124 C>T and c.-146 C>T TERT mutations and to genotype the rs2853669 polymorphism in a series of 68 soft tissue sarcomas (STS) comprising 22 histological subtypes.
PCR was performed, followed by direct sequencing of a fragment of TERT containing the hotspots and the rs2853669.
We found TERT mutations in 4/68 (5.9%) STSs including 1 pleomorphic liposarcoma (1/1), 1 dedifferentiated liposarcoma (1/1) and 2 myxoid liposarcomas (2/9). The variant C allele of rs2853669 was found in 54.8% (34/62) of all STSs and in 75% (3/4) of TERT-mutated cases. TERT mutations were associated with younger age, and the C allele of the rs2853669 was associated with high histological grade (2 and 3). No association was found between TERT mutation status or rs2853669 genotype and patient prognosis.
We showed that TERT promoter mutation is not a recurrent event in STS and is present in particular histological subtypes.
在几种癌症类型中,已发现端粒酶逆转录酶(TERT)基因启动子区域的致癌热点突变与较差的预后相关。此外,据报道TERT启动子区域的一种多态性(rs2853669)会影响TERT突变患者的生存率。我们的目的是确定68例软组织肉瘤(STS)(包括22种组织学亚型)中c.-124 C>T和c.-146 C>T TERT突变的频率,并对rs2853669多态性进行基因分型。
进行聚合酶链反应(PCR),随后对包含热点和rs2853669的TERT片段进行直接测序。
我们在4/68(5.9%)的STS中发现了TERT突变,包括1例多形性脂肪肉瘤(1/1)、1例去分化脂肪肉瘤(1/1)和2例黏液样脂肪肉瘤(2/9)。在所有STS的54.8%(34/62)和TERT突变病例的75%(3/4)中发现了rs2853669的变异C等位基因。TERT突变与较年轻的年龄相关,rs2853669的C等位基因与高组织学分级(2级和3级)相关。未发现TERT突变状态或rs2853669基因型与患者预后之间存在关联。
我们表明TERT启动子突变在STS中并非常见事件,且存在于特定的组织学亚型中。