Genomic mutation signatures in primary breast cancer and their axillary metastatic lymph nodes

X. Meng, Wenyan Wang, Jiaqi Liu, Shan Zheng, Changyuan Guo, Jie Wang, Z. Xing, Menglu Zhang, K. Feng, X. Wang, Xiang Wang
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Abstract

Abstract Breast cancer is one of the most common malignant tumors in women all over the world. Metastasis represents a major adverse progression of breast cancer, resulting in poor survival duration. Axillary lymph node metastasis is often the first step of systemic metastasis process of breast cancer. However, the mechanism of lymph node metastasis and the genomic signatures of primary breast tumors and lymph node metastasis are still under exploration. Whole exome sequencing was applied to primary breast cancer, axillary metastatic lymph nodes, and white blood cells from 10 Chinese women patients in our study. Single nucleotide variants (SNVs) and copy-number variants (CNVs) were compared between primary tumors and lymph nodes for individual patients. There are somatic SNVs (average 5.58 ± 2.56 per megabase) in primary breast cancers and somatic SNVs (average 5.46 ± 2.66 per megabase) in axillary metastatic lymph nodes were identified, which is corresponding to a semblable mutation burden in two malignant sites (P = 0.81). No difference was found in CNVs (P = 0.33). In primary breast cancer, somatic SNVs (48.12 ± 13.80%) and CNVs (61.72 ± 35.00%) were overlapping with somatic SNVs (49.43 ± 12.30%) and CNVs (72.01 ± 24.31%) in axillary metastatic lymph nodes. Nine genes were screened for significant specific mutations in primary tumors, and 15 genes were significantly mutated in metastatic lymph nodes. Using MutSigCV screening, it was found that HRNR and AHNAK2 are lymph node metastasis-specific genes. In our study, primary breast tumors are directly related to axillary lymph node metastases together and there are most SNVs and CNVs which were overlapping in primary and metastatic sites. These variants which are overlapping is closely related to the metastatic process of tumor invasion with early genetic variability. This is the first time to prove the concept of polyclonal metastatic model and in this model more than one clone migrates establish the metastases to axillary lymph nodes. This study was approved by the institutional review board (IRB) of the Cancer Hospital, Chinese Academy of Medical Sciences, and Peking Union Medical College, China (approval No. NCC2016G-030) on March 3, 2016.
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原发性乳腺癌及其腋窝转移性淋巴结的基因组突变特征
摘要乳腺癌是世界范围内女性最常见的恶性肿瘤之一。转移是乳腺癌的主要不良进展,导致生存时间较短。腋窝淋巴结转移往往是乳腺癌全身转移的第一步。然而,淋巴结转移的机制以及原发性乳腺肿瘤和淋巴结转移的基因组特征仍在探索中。全外显子组测序应用于10例中国女性患者的原发性乳腺癌、腋窝转移性淋巴结和白细胞。比较单个患者原发肿瘤和淋巴结的单核苷酸变异(SNVs)和拷贝数变异(CNVs)。原发性乳腺癌中存在体细胞snv(平均5.58±2.56 /兆碱基),腋窝转移淋巴结中存在体细胞snv(平均5.46±2.66 /兆碱基),这与两个恶性部位的相似突变负担相对应(P = 0.81)。两组CNVs无差异(P = 0.33)。原发性乳腺癌腋窝转移淋巴结的体细胞SNVs(48.12±13.80%)和CNVs(61.72±35.00%)与体细胞SNVs(49.43±12.30%)和CNVs(72.01±24.31%)重叠。9个基因在原发肿瘤中有显著特异性突变,15个基因在转移性淋巴结中有显著突变。通过MutSigCV筛选,发现HRNR和AHNAK2是淋巴结转移特异性基因。在我们的研究中,乳腺原发肿瘤与腋窝淋巴结转移有直接关系,并且在原发部位和转移部位snv和cnv的重叠最多。这些重叠的变异与肿瘤侵袭的转移过程密切相关,具有早期遗传变异性。这是第一次证明多克隆转移模型的概念,并且在该模型中多个克隆迁移建立转移到腋窝淋巴结。本研究经中国医学科学院肿瘤医院和中国北京协和医学院机构审查委员会(IRB)批准(批准号:NCC2016G-030)于2016年3月3日发布。
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