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通过阵列比较基因组杂交鉴定的基因组改变作为他莫昔芬治疗的雌激素受体阳性乳腺癌的预后标志物。

Genomic alterations identified by array comparative genomic hybridization as prognostic markers in tamoxifen-treated estrogen receptor-positive breast cancer.

作者信息

Han Wonshik, Han Mi-Ryung, Kang Jason Jongho, Bae Ji-Yeon, Lee Ji Hyun, Bae Young Ju, Lee Jeong Eon, Shin Hyuk-Jae, Hwang Ki-Tae, Hwang Sung-Eun, Kim Sung-Won, Noh Dong-Young

机构信息

Department of Surgery, Seoul National University College of Medicine, Seoul, Korea.

出版信息

BMC Cancer. 2006 Apr 12;6:92. doi: 10.1186/1471-2407-6-92.

Abstract

BACKGROUND

A considerable proportion of estrogen receptor (ER)-positive breast cancer recurs despite tamoxifen treatment, which is a serious problem commonly encountered in clinical practice. We tried to find novel prognostic markers in this subtype of breast cancer.

METHODS

We performed array comparative genomic hybridization (CGH) with 1,440 human bacterial artificial chromosome (BAC) clones to assess copy number changes in 28 fresh-frozen ER-positive breast cancer tissues. All of the patients included had received at least 1 year of tamoxifen treatment. Nine patients had distant recurrence within 5 years (Recurrence group) of diagnosis and 19 patients were alive without disease at least 5 years after diagnosis (Non-recurrence group).

RESULTS

Potential prognostic variables were comparable between the two groups. In an unsupervised clustering analysis, samples from each group were well separated. The most common regions of gain in all samples were 1q32.1, 17q23.3, 8q24.11, 17q12-q21.1, and 8p11.21, and the most common regions of loss were 6q14.1-q16.3, 11q21-q24.3, and 13q13.2-q14.3, as called by CGH-Explorer software. The average frequency of copy number changes was similar between the two groups. The most significant chromosomal alterations found more often in the Recurrence group using two different statistical methods were loss of 11p15.5-p15.4, 1p36.33, 11q13.1, and 11p11.2 (adjusted p values < 0.001). In subgroup analysis according to lymph node status, loss of 11p15 and 1p36 were found more often in Recurrence group with borderline significance within the lymph node positive patients (adjusted p = 0.052).

CONCLUSION

Our array CGH analysis with BAC clones could detect various genomic alterations in ER-positive breast cancers, and Recurrence group samples showed a significantly different pattern of DNA copy number changes than did Non-recurrence group samples.

摘要

背景

尽管接受了他莫昔芬治疗,但相当一部分雌激素受体(ER)阳性乳腺癌仍会复发,这是临床实践中常见的严重问题。我们试图在这种乳腺癌亚型中寻找新的预后标志物。

方法

我们使用1440个人类细菌人工染色体(BAC)克隆进行阵列比较基因组杂交(CGH),以评估28个新鲜冷冻的ER阳性乳腺癌组织中的拷贝数变化。所有纳入的患者均接受了至少1年的他莫昔芬治疗。9例患者在诊断后5年内出现远处复发(复发组),19例患者在诊断后至少5年无病存活(非复发组)。

结果

两组之间潜在的预后变量具有可比性。在无监督聚类分析中,每组的样本分得很开。根据CGH-Explorer软件的分析,所有样本中最常见的扩增区域是1q32.1、17q23.3、8q24.11、17q12 - q21.1和8p11.21,最常见的缺失区域是6q14.1 - q16.3、11q21 - q24.3和13q13.2 - q14.3。两组之间拷贝数变化的平均频率相似。使用两种不同统计方法在复发组中更常发现的最显著染色体改变是11p15.5 - p15.4、1p36.33、11q13.1和11p11.2的缺失(校正p值<0.001)。在根据淋巴结状态进行的亚组分析中,在淋巴结阳性患者中,复发组中11p15和1p36的缺失更常见,具有临界显著性(校正p = 0.052)。

结论

我们使用BAC克隆进行的阵列CGH分析可以检测ER阳性乳腺癌中的各种基因组改变,并且复发组样本显示出与非复发组样本明显不同的DNA拷贝数变化模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c1d/1459182/25c5001a7281/1471-2407-6-92-1.jpg

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