Baljevic Muhamed, Dumitriu Bogdan, Lee Ju-Whei, Paietta Elisabeth M, Wiernik Peter H, Racevskis Janis, Chen Christina, Stein Eytan M, Gallagher Robert E, Rowe Jacob M, Appelbaum Frederick R, Powell Bayard L, Larson Richard A, Coutré Steven E, Lancet Jeffrey, Litzow Mark R, Luger Selina M, Young Neal S, Tallman Martin S
Oncology/Hematology Division, The University of Nebraska Medical Center, Omaha, Nebr., USA.
Acta Haematol. 2016;136(4):210-218. doi: 10.1159/000448160. Epub 2016 Sep 16.
Telomeres are the capping ends of chromosomes that protect the loss of genetic material and prevent chromosomal instability. In human tissue-specific stem/progenitor cells, telomere length (TL) is maintained by the telomerase complex, which consists of a reverse transcriptase catalytic subunit (TERT) and an RNA template (TERC). Very short telomeres and loss-of-function mutations in the TERT and TERC genes have been reported in acute myeloid leukemia, but the role of telomeres in acute promyelocytic leukemia (APL) has not been well established. We report the results for a large cohort of 187 PML/RARα-positive APL patients. No germline mutations in the TERT or TERC genes were identified. Codon 279 and 1062 TERT polymorphisms were present at a frequency similar to that in the general population. TL measured in blood or marrow mononuclear cells at diagnosis was significantly shorter in the APL patients than in healthy volunteers, and shorter telomeres at diagnosis were significantly associated with high-risk disease. For patients who achieved complete remission, the median increase in TL from diagnosis to remission (delta TL) was 2.0 kilobase (kb), and we found delta TL to be the most powerful predictor of overall survival when compared with well-established risk factors for poor outcomes in APL.
端粒是染色体的帽状末端,可保护遗传物质不丢失并防止染色体不稳定。在人类组织特异性干细胞/祖细胞中,端粒长度(TL)由端粒酶复合体维持,该复合体由逆转录酶催化亚基(TERT)和RNA模板(TERC)组成。急性髓系白血病中已报道了非常短的端粒以及TERT和TERC基因的功能丧失突变,但端粒在急性早幼粒细胞白血病(APL)中的作用尚未明确。我们报告了187例PML/RARα阳性APL患者的大样本队列研究结果。未发现TERT或TERC基因的种系突变。密码子279和1062的TERT多态性出现频率与普通人群相似。诊断时在血液或骨髓单个核细胞中测量的TL在APL患者中显著短于健康志愿者,且诊断时较短的端粒与高危疾病显著相关。对于达到完全缓解的患者,从诊断到缓解时TL的中位数增加量(ΔTL)为2.0千碱基(kb),并且我们发现与APL预后不良的既定危险因素相比,ΔTL是总生存期最有力的预测指标。