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中国江西省乳腺癌患者中地中海贫血的患病率及基因紊乱谱

The prevalence and genetic disorders spectrum of thalassemia among breast cancer patients in Jiangxi province, China.

作者信息

Ding Jingxian, Huang Zhaohui, Jiang Xiaoliu, Li Qingge, Cao Yali, Guo Yonghong

机构信息

Department of Radiation Oncology, The Breast Cancer Institute, The Third Hospital of Nanchang, Nanchang, China.

Department of Breast Surgery, The Breast Cancer Institute, The Third Hospital of Nanchang, Nanchang, China.

出版信息

Front Genet. 2022 Oct 18;13:1001369. doi: 10.3389/fgene.2022.1001369. eCollection 2022.

Abstract

Thalassemia is a common inherited hematological disease with genetic disorders characterized by imbalanced synthesis of the globin chains. Due to the improvement of treatment methods, patients with thalassemia can survive for a long time. Therefore, it is not uncommon for patients with thalassemia suffering from malignant tumors. However, there are quite few reports on thalassemia patients complicated with breast cancer. Herein, we try to investigate the prevalence and genetic disorders spectrum of thalassemia in patients with breast cancer. Blood routing tests and serum ferritin analysis were conducted in 1887 breast cancer patients treated in the department of radiation oncology during 1 April 2020 and 30 March 2022. The suspected thalassemia carriers with small mean corpuscular volume (MCV), mean corpuscular hemoglobin content (MCH) or mean corpuscular hemoglobin concentration (MCHC) but the concentration of serum ferritin within normal limits were further investigated by polymerase chain reaction (PCR) and flow through hybridization gene chip to detect common mutations of α-globin and β-globin genes using Thalassemia Geno Array Diagnostic Kit. The prevalence and genetic mutation spectrum of thalassemia among breast cancer patients were analyzed. Four hundred and eighty-nine suspected thalassemia carriers were detected by complete blood cell counts and serum ferritin analysis among 1887 breast cancer patients. One hundred and seven cases (5.7%) were identified as carriers of thalassemia, of which 55 cases (51.4%) were α-thalassemia, 50 cases (46.7%) were β-thalassemia, and 2 cases (1.9%) were co-inheritance of α-thalassemia and β-thalassemia simultaneously. In α-thalassemia, the most prevalent genotype is -/αα; as for β-thalassemia, β/β is the most common genotype. The degree of anemia is more severe in β-thalassemia than in α-thalassemia. This is the first comprehensive molecular epidemiological investigation on thalassemia among breast cancer patients. Our data indicated that thalassemia was not uncommon in breast cancer patients. The physicians should have the knowledge to avoid misdiagnosis as iron deficiency anemia.

摘要

地中海贫血是一种常见的遗传性血液疾病,属于遗传性疾病,其特征是珠蛋白链合成失衡。由于治疗方法的改进,地中海贫血患者能够长期存活。因此,地中海贫血患者罹患恶性肿瘤并不罕见。然而,关于地中海贫血患者合并乳腺癌的报道相当少。在此,我们试图调查乳腺癌患者中地中海贫血的患病率和基因紊乱谱。对2020年4月1日至2022年3月31日在放疗科接受治疗的1887例乳腺癌患者进行了血常规检查和血清铁蛋白分析。对平均红细胞体积(MCV)、平均红细胞血红蛋白含量(MCH)或平均红细胞血红蛋白浓度(MCHC)较小但血清铁蛋白浓度在正常范围内的疑似地中海贫血携带者,采用聚合酶链反应(PCR)和流式杂交基因芯片,使用地中海贫血基因阵列诊断试剂盒检测α-珠蛋白和β-珠蛋白基因的常见突变。分析了乳腺癌患者中地中海贫血的患病率和基因突变谱。在1887例乳腺癌患者中,通过全血细胞计数和血清铁蛋白分析检测出489例疑似地中海贫血携带者。其中107例(5.7%)被确定为地中海贫血携带者,其中55例(51.4%)为α-地中海贫血,50例(46.7%)为β-地中海贫血,2例(1.9%)为α-地中海贫血和β-地中海贫血同时遗传。在α-地中海贫血中,最常见的基因型是 -/αα;至于β-地中海贫血,β/β是最常见的基因型。β-地中海贫血的贫血程度比α-地中海贫血更严重。这是首次对乳腺癌患者中的地中海贫血进行全面的分子流行病学调查。我们的数据表明,地中海贫血在乳腺癌患者中并不罕见。医生应具备相关知识,避免误诊为缺铁性贫血。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11cc/9623098/f13ab49d0756/fgene-13-1001369-g001.jpg

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