Balachandar V, Lakshman Kumar B, Sasikala K, Manikantan P, Sangeetha R, Mohana Devi S
Division of Human Genetics, Department of Zoology, Bharathiar University, Coimbatore-641046, Tamilnadu, India.
J Zhejiang Univ Sci B. 2007 Sep;8(9):638-46. doi: 10.1631/jzus.2007.B0638.
The aim of the present investigation was to study the major chromosomal aberrations (CA) like deletion, translocation, inversion and mosaic in prostate cancer patients of Tamilnadu, Southern India. Totally 45 blood samples were collected from various hospitals in Tamilnadu, Southern India. Equal numbers of normal healthy subjects were chosen after signing a consent form. Volunteers provided blood samples (5 ml) to establish leukocyte cultures. Cytogenetic studies were performed by using Giemsa-banding technique and finally the results were ensured by spectral karyotyping (SKY) technique. In the present investigation, major CA like deletion, translocation, inversion and mosaic were identified in experimental subjects. Results showed frequent CA in chromosomes 1, 3, 5, 6, 7, 9, 13, 16, 18 and X. In comparison with experimental subjects, the control subjects exhibited very low levels of major CA (P<0.05). In the present study, the high frequency of centromeric rearrangements indicates a potential role for mitotic irregularities associated with the centromere in prostate cancer tumorigenesis. Identification of chromosome alterations may be helpful in understanding the molecular basis of the disease in better manner.
本研究的目的是研究印度南部泰米尔纳德邦前列腺癌患者中的主要染色体畸变(CA),如缺失、易位、倒位和嵌合体。从印度南部泰米尔纳德邦的多家医院共采集了45份血样。在签署知情同意书后,选取了数量相等的正常健康受试者。志愿者提供血样(5毫升)以建立白细胞培养物。采用吉姆萨染色技术进行细胞遗传学研究,最后通过光谱核型分析(SKY)技术确认结果。在本研究中,在实验对象中鉴定出了缺失、易位、倒位和嵌合体等主要染色体畸变。结果显示,1、3、5、6、7、9、13、16、18号染色体和X染色体上频繁出现染色体畸变。与实验对象相比,对照对象的主要染色体畸变水平非常低(P<0.05)。在本研究中,着丝粒重排的高频率表明着丝粒相关的有丝分裂异常在前列腺癌肿瘤发生中具有潜在作用。鉴定染色体改变可能有助于更好地理解该疾病的分子基础。