Kurvinen Kaisa, Rantanen Virpi, Syrjänen Stina, Johansson Bo
Department of Oral Pathology and Oral Radiology, Institute of Dentistry and MediCity Research Laboratory, Faculty of Medicine, University of Turku, Turku, Finland.
Int J Radiat Biol. 2006 Dec;82(12):859-67. doi: 10.1080/09553000600969812.
Telomerase activation in response to irradiation might enhance the radioresistance of cells. Thus, we have investigated radiation-induced effects on telomerase in six gynecological cancer cell lines, with different intrinsic radiosensitivity and capacity for sublethal damage repair (SLDR).
Three endometrial adenocarcinoma (UM-EC-1, UT-EC-2B and UT-EC-3) and three vulvar squamous cell carcinoma (A431, UM-SCV-2 and UM-SCV-7) cell lines were irradiated with doses of 5, 10 and 25 Gy and the effects on telomerase were evaluated at 0.5, 6, 24 and 48 h post-irradiation. Telomerase activity was quantitatively measured by SYBR Green real-time telomeric repeat amplification protocol.
The most radioresistant cell line A431 had the strongest stimulatory effects (approximately 2.0 - 2.5-fold) on telomerase activity 24 and 48 h post-irradiation with the highest radiation doses. In contrast to that, telomerase activities in the highly radiosensitive cell line UT-EC-2B remained below the basal level throughout the 48-h period of post-irradiation with the highest doses, and even a decline to approximately 50% of the basal level was found 24 h after exposure. In other cell lines being either moderately or highly radiation resistant, telomerase activity levels in response to irradiation remained mainly at the basal level or gradually increased.
The present findings indicate that there might be a connection between the radiation-induced telomerase response and radiosensitivity. However, no correlation was found between the radiation-induced effects on telomerase and the sublethal damage repair capacity of the cells.
响应辐射的端粒酶激活可能增强细胞的放射抗性。因此,我们研究了辐射对六种妇科癌细胞系中端粒酶的影响,这些细胞系具有不同的内在放射敏感性和亚致死损伤修复(SLDR)能力。
用5、10和25 Gy的剂量照射三种子宫内膜腺癌(UM-EC-1、UT-EC-2B和UT-EC-3)和三种外阴鳞状细胞癌(A431、UM-SCV-2和UM-SCV-7)细胞系,并在照射后0.5、6、24和48小时评估对端粒酶的影响。通过SYBR Green实时端粒重复扩增协议定量测量端粒酶活性。
放射抗性最强的细胞系A431在接受最高辐射剂量照射后24和48小时对端粒酶活性具有最强的刺激作用(约2.0 - 2.5倍)。与此相反,放射敏感性高的细胞系UT-EC-2B在接受最高剂量照射后的48小时内端粒酶活性一直低于基础水平,甚至在照射后24小时发现下降至基础水平的约50%。在其他中度或高度放射抗性的细胞系中,辐射诱导的端粒酶活性水平主要保持在基础水平或逐渐增加。
目前的研究结果表明,辐射诱导的端粒酶反应与放射敏感性之间可能存在联系。然而,未发现辐射对端粒酶的影响与细胞的亚致死损伤修复能力之间存在相关性。