Cancer risk assessment of premalignant breast tissues from patients with BRCA mutations by genome profiling.

IF 6.5 2区 医学 Q1 ONCOLOGY NPJ Breast Cancer Pub Date : 2024-10-04 DOI:10.1038/s41523-024-00693-9
Takeshi Hirose, Masachika Ikegami, Kumiko Kida, Toshihide Ueno, Rina Kitada, Lei Wang, Shinya Tanaka, Makoto Endo, Yasuharu Nakashima, Naoki Kanomata, Hiroyuki Mano, Hideko Yamauchi, Shinji Kohsaka
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Abstract

Patients with germline pathogenic variants of BRCA1/2 genes have a particular predisposition to develop breast cancer. No clinical test has been developed to accurately and quantitatively evaluate their risk of developing breast cancer. We hypothesized that aberrant cell clonal expansion may be initiated in normal breast tissues without manifesting pathologic changes. To assess the prevalence of clonal expansion in the normal breast, we collected normal breast tissue from 24 breast cancer patients who had undergone surgical resection and 5 carriers of pathogenic BRCA1/2 variant who had undergone prophylactic mastectomy. Whole-exome sequencing (WES) was conducted in 97 specimens from 14 individuals, and TOP panel, a gene panel targeting 464 genes, was conducted in 321 specimens from 26 individuals, including 8 individuals with germline pathogenic variants of BRCA1/2 genes. Recurrent oncogenic mutations within PIK3CA, ARHGAP35, HRAS, and NF1 were identified in normal breast tissue at considerable variant allelic frequencies (VAF), suggesting clonal expansion. In addition, 937 normal breast tissues were evaluated using the Breast Cancer Panel (BCP) targeting 25 genes to determine the exact prevalence and distribution of clonal expansion. To assess the clonal expansion, we developed the clonality score, which is the mean value of clonal cell fractions for samples obtained from a given breast. The average clonality score in macroscopically normal breast tissue was 0.95 (0-2.46), with a significant difference between cases with and without a history of breast cancer of stage 2 or more advanced stage (p = 0.01). Additional WES on 42 samples with relatively large clone size (VAF > 3%) confirmed that these cell clones harbored multiple mutations (10.7 mutations/sample), and the number of existing mutations was consistent with the clone size (R = 0.50). The results suggest that clonal changes occur in normal breast tissue of women at high risk for breast cancer even before cancer is detected pathologically and/or radiologically, and the clonality score shows the potential to be a valid method of evaluating clonal expansion for cancer-risk assessment that provides appropriate preventive options for patients at high risk for breast cancer.

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通过基因组图谱对 BRCA 基因突变患者的恶性前乳腺组织进行癌症风险评估。
具有 BRCA1/2 基因种系致病变异的患者特别容易罹患乳腺癌。目前还没有一种临床检测方法能准确、定量地评估他们罹患乳腺癌的风险。我们假设,正常乳腺组织中可能存在异常细胞克隆扩增,但不会出现病理变化。为了评估克隆扩增在正常乳腺中的发生率,我们收集了 24 名接受过手术切除的乳腺癌患者和 5 名接受过预防性乳房切除术的 BRCA1/2 变异致病携带者的正常乳腺组织。对来自 14 人的 97 份标本进行了全外显子组测序(WES),并对来自 26 人的 321 份标本(包括 8 名 BRCA1/2 基因种系致病变异者)进行了针对 464 个基因的 TOP panel 测序。在正常乳腺组织中发现了PIK3CA、ARHGAP35、HRAS和NF1中的复发性致癌突变,其变异等位基因频率(VAF)相当高,表明存在克隆扩增。此外,我们还使用针对 25 个基因的乳腺癌面板(BCP)对 937 个正常乳腺组织进行了评估,以确定克隆扩增的确切发生率和分布情况。为了评估克隆扩增,我们制定了克隆度评分,即从特定乳腺样本中获得的克隆细胞分数的平均值。宏观正常乳腺组织的克隆度平均值为 0.95(0-2.46),有乳腺癌 2 期或更晚期病史的病例与无乳腺癌病史的病例之间存在显著差异(p = 0.01)。对 42 个克隆体积相对较大(VAF > 3%)的样本进行的额外 WES 证实,这些细胞克隆存在多个突变(10.7 个突变/样本),现有突变的数量与克隆体积一致(R = 0.50)。结果表明,乳腺癌高危女性的正常乳腺组织甚至在病理和/或放射学检测出癌症之前就发生了克隆变化,而克隆性评分显示出它有可能成为评估克隆扩增的有效方法,用于癌症风险评估,为乳腺癌高危患者提供适当的预防方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
NPJ Breast Cancer
NPJ Breast Cancer Medicine-Pharmacology (medical)
CiteScore
10.10
自引率
1.70%
发文量
122
审稿时长
9 weeks
期刊介绍: npj Breast Cancer publishes original research articles, reviews, brief correspondence, meeting reports, editorial summaries and hypothesis generating observations which could be unexplained or preliminary findings from experiments, novel ideas, or the framing of new questions that need to be solved. Featured topics of the journal include imaging, immunotherapy, molecular classification of disease, mechanism-based therapies largely targeting signal transduction pathways, carcinogenesis including hereditary susceptibility and molecular epidemiology, survivorship issues including long-term toxicities of treatment and secondary neoplasm occurrence, the biophysics of cancer, mechanisms of metastasis and their perturbation, and studies of the tumor microenvironment.
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