Kim Jun Hyun, Lee Gun Eui, Kim Jin Cheon, Lee Jun Ho, Chung In Kwon
Department of Biology and Protein Network Research Center, Yonsei University, Seoul, Korea.
Mol Cells. 2002 Apr 30;13(2):228-36.
Actively dividing cells show progressive loss of telomeric DNA during successive rounds of replication due to end-replication problem. Telomere shortening has been proposed as a regulatory mechanism that controls the replicative capacity of primary cells before undergoing cellular senescence. In immortal cells including cancer, cellular senescence can be overcome by reactivation of telomerase or by a telomerase-independent mechanism for lengthening telomeres. In this work, we present a novel example of telomere elongation mechanism in a human stomach adenocarcinoma cell line which was selected for resistance to adriamycin. The resistant cell line (MKN/ADR) had long terminal restriction fragments (TRFs) of up to approximately 50 kb, while its parent cell line (MKN-45) had the TRFs, consisting of a smear extending from approximately 4 to approximately 25 kb. The very large TRFs in MKN/ADR cell line were proven to be telomeric by digestion with the exonuclease Bal31. When telomerase activity was examined using the PCR-based telomeric repeat amplification protocol (TRAP) assay, MKN/ADR cell line showed reduced activity to about 10% of that in MKN-45 cell line. The correlation between reduced telomerase activity and mRNA expression of telomerase subunits in MKN/ADR cell line was assessed by the reverse transcriptase-PCR analysis. The level of human telomerase reverse transcriptase (hTERT) mRNA was lower in MKN/ADR cell line than in MKN-45 cell line. This observation correlates with the finding that telomerase activity is reduced about 10-fold in MKN/ADR cell line. Reverse transcriptase-PCR analysis also revealed a close correlation between telomerase-associated protein (TP1) mRNA expression and telomerase activity in MKN/ADR cell line. In contrast, expression levels of human telomerase RNA (hTR) were identical in both MKN/ADR and MKN-45 cell lines. Taken together, these data suggest that telomeres in MKN/ADR cell line may be regulated through a novel mechanism other than telomerase. Although the basis for telomere elongation mechanism in MKN/ADR cell line is not yet understood, the occurrence of alternative mechanism for telomere elongation in drug-resistant cancer cells may have an important implication for use of telomerase inhibitors in human cancer treatment.
由于末端复制问题,处于活跃分裂状态的细胞在连续的复制轮次中会出现端粒DNA的逐渐丢失。端粒缩短被认为是一种调控机制,可在原代细胞进入细胞衰老之前控制其复制能力。在包括癌细胞在内的永生细胞中,细胞衰老可通过端粒酶的重新激活或通过一种不依赖端粒酶的端粒延长机制来克服。在这项研究中,我们展示了在一种对阿霉素具有抗性的人胃腺癌细胞系中端粒延长机制的一个新例子。抗性细胞系(MKN/ADR)具有长达约50 kb的长末端限制片段(TRF),而其亲本细胞系(MKN-45)的TRF由从约4 kb延伸至约25 kb的条带组成。通过核酸外切酶Bal31消化证明,MKN/ADR细胞系中非常大的TRF是端粒。当使用基于PCR的端粒重复序列扩增协议(TRAP)分析检测端粒酶活性时,MKN/ADR细胞系的活性降低至MKN-45细胞系的约10%。通过逆转录酶-PCR分析评估了MKN/ADR细胞系中端粒酶活性降低与端粒酶亚基mRNA表达之间的相关性。MKN/ADR细胞系中人端粒酶逆转录酶(hTERT)mRNA的水平低于MKN-45细胞系。这一观察结果与MKN/ADR细胞系中端粒酶活性降低约10倍的发现相关。逆转录酶-PCR分析还揭示了MKN/ADR细胞系中端粒酶相关蛋白(TP1)mRNA表达与端粒酶活性之间的密切相关性。相比之下,人端粒酶RNA(hTR)在MKN/ADR和MKN-45细胞系中的表达水平相同。综上所述,这些数据表明MKN/ADR细胞系中的端粒可能通过一种不同于端粒酶的新机制进行调控。尽管MKN/ADR细胞系中端粒延长机制的基础尚不清楚,但耐药癌细胞中端粒延长替代机制的出现可能对人类癌症治疗中端粒酶抑制剂的使用具有重要意义。