Mol. Cells 2002; 13(2): 228-236
Published online January 1, 1970
© The Korean Society for Molecular and Cellular Biology
Actively dividing cells show progressive loss of telom-eric DNA during successive rounds of replication due to end-replication problem. Telomere shortening has been proposed as a regulatory mechanism that con-trols the replicative capacity of primary cells before undergoing cellular senescence. In immortal cells in-cluding 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 adenocar-cinoma cell line which was selected for resistance to adriamycin. The resistant cell line (MKN/ADR) had long terminal restriction fragments (TRFs) of up to ~50 kb, while its parent cell line (MKN-45) had the TRFs, consisting of a smear extending from ~4 to ~25 kb. The very large TRFs in MKN/ADR cell line were proven to be telomeric by digestion with the exonucle-ase 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 ac-tivity and mRNA expression of telomerase subunits in MKN/ADR cell line was assessed by the reverse tran-scriptase-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 pro-tein (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 telom-erase inhibitors in human cancer treatment.
Keywords T, Immortalization, Adriamycin-resistant Cell Line
Mol. Cells 2002; 13(2): 228-236
Published online April 30, 2002
Copyright © The Korean Society for Molecular and Cellular Biology.
Jun Hyun Kim, Gun Eui Lee, Jin Cheon Kim, Jun Ho Lee, In Kwon Chung
Actively dividing cells show progressive loss of telom-eric DNA during successive rounds of replication due to end-replication problem. Telomere shortening has been proposed as a regulatory mechanism that con-trols the replicative capacity of primary cells before undergoing cellular senescence. In immortal cells in-cluding 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 adenocar-cinoma cell line which was selected for resistance to adriamycin. The resistant cell line (MKN/ADR) had long terminal restriction fragments (TRFs) of up to ~50 kb, while its parent cell line (MKN-45) had the TRFs, consisting of a smear extending from ~4 to ~25 kb. The very large TRFs in MKN/ADR cell line were proven to be telomeric by digestion with the exonucle-ase 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 ac-tivity and mRNA expression of telomerase subunits in MKN/ADR cell line was assessed by the reverse tran-scriptase-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 pro-tein (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 telom-erase inhibitors in human cancer treatment.
Keywords: T, Immortalization, Adriamycin-resistant Cell Line
Xun Jin, Joong-Seob Lee, Sungwook Kwak, Soo-Yeon Lee, Ji-Eun Jung, Tae-Kyung Kim, Chenxiong Xu, Zhongshan Hong, Zhehu Li, Sun-Myung Kim, Xumin Pian, Dong-Hee Lee, Jong-Taek Yoon, Seungkwon You, Yun-Jaie Choi, Hyunggee Kim
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