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苯致白血病患者血小板线粒体突变的基因组分析:病例报告。

Genomic analysis of mutations in platelet mitochondria in a case of benzene-induced leukaemia: A case report.

机构信息

Shenzhen Prevention and Treatment Center for Occupational Diseases, Shenzhen, Guangdong.

Hebei North University, Hebei, China.

出版信息

Medicine (Baltimore). 2021 Jan 8;100(1):e24014. doi: 10.1097/MD.0000000000024014.

Abstract

INTRODUCTION

As a hematopoietic carcinogen, benzene induces human leukemia through its active metabolites such as benzoquinone, which may cause oxidative damage to cancer-related nuclear genes by increasing reactive oxygen species (ROS). Mitochondrion is the main regulatory organelle of ROS, genetic abnormality of mitochondrion can impede its regulation of ROS, leading to more severe oxidative damage. Mutations have been related to certain types of cancer in several mitochondrial genes, but they have never been completely analyzed genome-wide in leukemia.

PATIENT CONCERNS

The patient was a 52-year-old female who had chronic exposure to benzene for several years. Her symptoms mainly included recurrent dizziness, fatigue, and they had lasted for nearly 8 years and exacerbated in recent weeks before diagnosis.

DIAGNOSIS

Samples of peripheral blood were taken from the patient using evacuated tubes with EDTA anticoagulant on the second day of her hospitalization. At the same time blood routine and BCR/ABL genes of leukemic phenotype were tested. Platelets were isolated for mitochondrial DNA (mtDNA) extraction. The genetic analysis of ATP synthase Fo subunit 8 (complex V), ATP synthase Fo subunit 6 (complex V), cytochrome c oxidase subunit 1 (complex IV), cytochrome c oxidase subunit 2 (complex IV), cytochrome c oxidase subunit 3, Cytb, NADH dehydrogenase subunit 1 (complex I) (ND) 1, ND2, ND3, ND4, ND5, ND6, 12S-RNA, 16S-RNA, tRNA-Cysteine, A, N, tRNA-Leucine, E, displacement loop in platelet mtDNA were performed. All the detected gene mutations were validated using the conventional Sanger sequencing method.

INTERVENTIONS

The patient received imatinib, a small molecule kinase inhibitor, and symptomatic treatments.

OUTCOMES

After 3 months treatment her blood routine test indicators were restored to normal.

CONCLUSION

A total of 98 mutations were found, and 25 mutations were frame shift. The ND6 gene mutation rate was the highest among all mutation points. Frame shifts were identified in benzene-induced leukemia for the first time. Many mutations in the platelet mitochondrial genome were identified and considered to be potentially pathogenic in the female patient with benzene-induced leukemia. The mutation rate of platelet mitochondrial genome in the benzene-induced leukemia patient is relatively high, and the complete genome analysis is helpful to fully comprehend the disease characteristics.

摘要

简介

苯是一种造血致癌物质,通过其活性代谢物如苯醌诱导人类白血病,这可能通过增加活性氧物种(ROS)对癌症相关核基因造成氧化损伤。线粒体是 ROS 的主要调节细胞器,线粒体的遗传异常可能会阻碍其对 ROS 的调节,导致更严重的氧化损伤。几个线粒体基因中的突变与某些类型的癌症有关,但它们从未在白血病中进行过全基因组的完全分析。

患者关注

患者为 52 岁女性,曾有多年慢性苯暴露史。她的症状主要包括反复发作的头晕、疲劳,这些症状已经持续了近 8 年,在确诊前几周加重。

诊断

患者住院第二天,使用含 EDTA 抗凝剂的真空采血管采集外周血样本。同时检测白血病表型的血常规和 BCR/ABL 基因。分离血小板提取线粒体 DNA(mtDNA)。对 ATP 合酶 Fo 亚基 8(复合物 V)、ATP 合酶 Fo 亚基 6(复合物 V)、细胞色素 c 氧化酶亚基 1(复合物 IV)、细胞色素 c 氧化酶亚基 2(复合物 IV)、细胞色素 c 氧化酶亚基 3、Cytb、NADH 脱氢酶亚基 1(复合物 I)(ND)1、ND2、ND3、ND4、ND5、ND6、12S-RNA、16S-RNA、tRNA-Cysteine、A、N、tRNA-Leucine、E、血小板 mtDNA 中的移位环进行基因检测。使用常规 Sanger 测序法验证所有检测到的基因突变。

干预

患者接受了小分子激酶抑制剂伊马替尼和对症治疗。

结果

治疗 3 个月后,患者血常规检查指标恢复正常。

结论

共发现 98 种突变,其中 25 种为移码突变。ND6 基因突变率在所有突变点中最高。首次在苯诱导的白血病中发现移码突变。在苯诱导的白血病女性患者中发现了许多血小板线粒体基因组的突变,并认为这些突变可能具有潜在的致病性。苯诱导的白血病患者血小板线粒体基因组的突变率相对较高,进行全基因组分析有助于全面了解疾病特征。

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