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软骨肉瘤中 hTERT 启动子突变与进展和疾病相关死亡率相关。

hTERT promoter mutations in chondrosarcomas associate with progression and disease-related mortality.

机构信息

Department of Oncology-Pathology, Cancer Centre Karolinska, Karolinska Institutet, Stockholm, Sweden.

Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.

出版信息

Mod Pathol. 2018 Dec;31(12):1834-1841. doi: 10.1038/s41379-018-0098-3. Epub 2018 Jul 31.

Abstract

Chondrosarcomas are malignant skeletal tumors with chondroid differentiation. Prognosis is largely dependent on histological grading, which suffer from significant interobserver variability. Telomerase activity and abundant telomerase reverse transcriptase (hTERT) expression has previously been associated with chondrosarcoma grade and metastasis. We therefore analyzed the hTERT promoter in clinicopathologically well-characterized chondrosarcomas (grade 1-3) from 87 patients. Using Sanger sequencing we identified an activating -124 C > T mutation in 23 cases (26%). Promoter mutations were significantly associated with increased histological grade (8% of grade 1, 32% of grade 2 and 46% of grade 3, P = 0.002), suggesting a role in tumor progression. In four chondrosarcomas where the histopathological grade was heterogenous, the hTERT mutation was only identified in the higher-grade areas. Additionally, hTERT promoter mutations were significantly associated with worse metastasis-free survival (P = 0.018), chondrosarcoma-specific survival (P = 0.022) and older patient age (P = 0.003). These data suggest that hTERT promoter mutations are common in high grade conventional chondrosarcomas. Granted that additional studies can confirm these findings; hTERT promoter analysis could potentially serve as an adjuvant prognostic marker in routine chondrosarcoma grading. This study reinforces the rationale of telomerase targeted therapy in a subset of chondrosarcomas.

摘要

软骨肉瘤是一种具有软骨分化的恶性骨骼肿瘤。预后在很大程度上取决于组织学分级,但该分级存在显著的观察者间变异性。端粒酶活性和丰富的端粒酶逆转录酶(hTERT)表达先前与软骨肉瘤分级和转移有关。因此,我们分析了 87 例临床病理特征明确的软骨肉瘤(1-3 级)的 hTERT 启动子。我们通过 Sanger 测序在 23 例(26%)中发现了一个激活的-124C>T 突变。启动子突变与组织学分级增加显著相关(1 级中为 8%,2 级中为 32%,3 级中为 46%,P=0.002),提示其在肿瘤进展中起作用。在 4 例组织病理学分级存在异质性的软骨肉瘤中,仅在高级别区域检测到 hTERT 突变。此外,hTERT 启动子突变与无转移生存(P=0.018)、软骨肉瘤特异性生存(P=0.022)和患者年龄较大(P=0.003)显著相关。这些数据表明,hTERT 启动子突变在高级别常规软骨肉瘤中很常见。如果进一步的研究可以证实这些发现;hTERT 启动子分析可能在常规软骨肉瘤分级中作为辅助预后标志物。这项研究强化了在软骨肉瘤亚组中针对端粒酶的治疗策略的合理性。

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