Malignant transformation in human chondrosarcoma cells supported by telomerase activation and tumor suppressor inactivation.

James A Martin, Erin Forest, Joel A Block, Aloysius J Klingelhutz, Brent Whited, Steven Gitelis, Andrew Wilkey, Joseph A Buckwalter
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Abstract

Human chondrosarcomas do not respond to current chemotherapies or radiation therapy, and their size and histological appearance do not reliably predict the risk of local recurrence and metastases, making selection of surgical treatment difficult. Identifying mechanisms responsible for the proliferation and invasive behavior of these tumors would be of immense clinical value. We hypothesized that telomerase expression is one of these mechanisms. We detected telomerase expression in 7 of 16 chondrosarcomas, but cells cultured from telomerase-negative chondrosarcomas acquired strong telomerase activity and lost tumor suppressor activity after their establishment in culture. These changes were associated with accelerated indefinite cell proliferation, morphological transition, and increased invasive activity, indicating that telomerase activation and loss of cell cycle control leads to the emergence of aggressive cells from chondrosarcoma cell populations. These observations may lead to better understanding of the factors responsible for malignant transformation, local recurrence, and metastases of cartilage neoplasms.

端粒酶激活和肿瘤抑制因子失活支持人软骨肉瘤细胞的恶性转化。
人软骨肉瘤对目前的化疗或放疗没有反应,而且它们的大小和组织学外观不能可靠地预测局部复发和转移的风险,这使得选择手术治疗变得困难。确定这些肿瘤的增殖和侵袭行为的机制将具有巨大的临床价值。我们假设端粒酶的表达是其中一种机制。我们在16个软骨肉瘤中的7个中检测到了端粒酶的表达,但从端粒酶阴性的软骨肉瘤培养的细胞在培养后获得了很强的端粒酶活性,而失去了抑瘤活性。这些变化与加速的不确定细胞增殖、形态转变和侵袭性活动增加有关,表明端粒酶激活和细胞周期控制的丧失导致软骨肉瘤细胞群中出现侵袭性细胞。这些观察结果可能有助于更好地了解导致软骨肿瘤恶性转化、局部复发和转移的因素。
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