Telomere Maintenance Mechanisms in Human Osteosarcoma

描述（申请人提供）：骨肉瘤是儿童和青少年最常见的原发性骨肿瘤。尽管在过去30年中治疗取得了重大进展，但大约30%的局限性疾病患者和60%的转移性疾病患者无法存活。需要新的预后指标和治疗靶点来改善骨肉瘤患者的预后。端粒是覆盖在染色体末端的核蛋白结构。在每一轮复制中，由于DNA聚合酶无法复制DNA的末端，端粒会受到侵蚀。当端粒变得极短时，细胞衰老或凋亡被诱导。癌细胞的一个特点是它们具有无限的增殖潜力。为了实现这一目标，他们必须开发出对抗端粒缩短的机制。大多数人类癌症激活端粒酶来维持端粒，但少数癌症使用一种定义不明确的机制，称为“端粒选择性延长”或“ALT”。骨肉瘤与大多数人类癌症不同，骨肉瘤通常使用ALT机制。实验室研究表明，与ALT相比，端粒酶的表达与增加的致瘤性和转移有关。这就提出了端粒酶依赖性骨肉瘤比alt依赖性骨肉瘤更具临床侵袭性的可能性。与儿童肿瘤组（COG）合作，本研究将评估端粒酶表达在非转移性骨肉瘤患者中的预后意义。此外，本研究将利用人骨肉瘤端粒维持机制的异质性来鉴定ALT的新生物标志物。

DESCRIPTION (provided by applicant): Osteosarcoma is the most common primary bone tumor of children and adolescents. Despite significant treatment advances over the past 30 years, approximately 30% of patients with localized disease and 60% of patients with metastatic disease do not survive. Novel prognostic markers and therapeutic targets are needed to improve the outcomes of patients with osteosarcoma. Telomeres are nucleoprotein structures that cap chromosome ends. With each round of replication, telomeres erode due to the inability of DNA polymerases to replicate the very ends of DNA. When telomeres become critically short, cellular senescence or apoptosis are induced. A hallmark of cancer cells is that they have unlimited proliferative potential. To achieve this, they must develop mechanisms to counteract telomere shortening. Most human cancers activate the enzyme telomerase to maintain telomeres, but a minority of cancers use a poorly defined mechanism called "alternative lengthening of telomeres," or "ALT." Osteosarcoma is dissimilar from most human cancers in that osteosarcomas commonly use the ALT mechanism. Laboratory studies have shown that compared to ALT, telomerase expression is associated with increased tumorigenicity and metastasis. This raises the possibility that the telomerase-dependent osteosarcomas are more clinically aggressive than their ALT-dependent counterparts. In collaboration with the Children's Oncology Group (COG), this study will evaluate the prognostic significance of telomerase expression in patients with non-metastatic osteosarcoma. In addition, this study will take advantage of the heterogeneity of telomere maintenance mechanisms in human osteosarcoma to identify novel biomarkers for ALT.