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Genomic aberrations in normal tissue adjacent to HER2-amplified breast cancers: field cancerization or contaminating tumor cells?

机译:与HER2扩增的乳腺癌相邻的正常组织中的基因组畸变:野癌或污染肿瘤细胞?

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摘要

Field cancerization effects as well as isolated tumor cell foci extending well beyond the invasive tumor margin have been described previously to account for local recurrence rates following breast conserving surgery despite adequate surgical margins and breast radiotherapy. To look for evidence of possible tumor cell contamination or field cancerization by genetic effects, a pilot study (Study 1: 12 sample pairs) followed by a verification study (Study 2: 20 sample pairs) were performed on DNA extracted from HER2-positive breast tumors and matching normal adjacent mammary tissue samples excised 1–3 cm beyond the invasive tumor margin. High-resolution molecular inversion probe (MIP) arrays were used to compare genomic copy number variations, including increased HER2 gene copies, between the paired samples; as well, a detailed histologic and immunohistochemical (IHC) re-evaluation of all Study 2 samples was performed blinded to the genomic results to characterize the adjacent normal tissue composition bracketing the DNA-extracted samples. Overall, 14/32 (44 %) sample pairs from both studies produced genome-wide evidence of genetic aberrations including HER2 copy number gains within the adjacent normal tissue samples. The observed single-parental origin of monoallelic HER2 amplicon haplotypes shared by informative tumor–normal pairs, as well as commonly gained loci elsewhere on 17q, suggested the presence of contaminating tumor cells in the genomically aberrant normal samples. Histologic and IHC analyses identified occult 25–200 μm tumor cell clusters overexpressing HER2 scattered in more than half, but not all, of the genomically aberrant normal samples re-evaluated, but in none of the genomically normal samples. These genomic and microscopic findings support the conclusion that tumor cell contamination rather than genetic field cancerization represents the likeliest cause of local clinical recurrence rates following breast conserving surgery, and mandate caution in assuming the genomic normalcy of histologically benign appearing peritumor breast tissue.Electronic supplementary materialThe online version of this article (doi:10.1007/s10549-012-2290-3) contains supplementary material, which is available to authorized users.
机译:先前已经描述了场癌变效应以及远远超出浸润性肿瘤边缘的孤立肿瘤细胞灶,以解释尽管有足够的手术边缘和乳房放疗,但在保乳手术后局部复发率高。为了寻找通过遗传效应可能导致肿瘤细胞污染或田野癌变的证据,对从HER2阳性乳腺癌中提取的DNA进行了先导研究(研究1:12个样品对),然后进行了验证研究(研究2:20个样品对)。肿瘤和相匹配的正常邻近乳腺组织样本在侵袭性肿瘤边缘以外1-3 cm处切除。使用高分辨率分子倒置探针(MIP)阵列比较配对样品之间的基因组拷贝数变异,包括增加的HER2基因拷贝。同样,对所有研究2样品进行了详细的组织学和免疫组化(IHC)重新评估,而对基因组结果不了解,以表征包围DNA提取样品的相邻正常组织组成。总体而言,两项研究的14/32(44%)对样本均产生了全基因组遗传异常证据,包括相邻正常组织样本中HER2拷贝数增加的现象。信息丰富的正常肿瘤对以及在17q处其他位置普遍获得的基因座所观察到的单等位基因HER2扩增子单倍型的单亲起源表明,在基因组异常的正常样品中存在污染性肿瘤细胞。组织学和IHC分析发现,隐匿的25-200μm肿瘤细胞簇过度表达了HER2,散布在超过一半(但不是全部)的基因组异常正常样本中,但没有对基因组正常样本进行重新评估。这些基因组学和微观研究结果支持这样的结论,即肿瘤细胞污染而不是遗传领域的癌变代表了保乳手术后局部临床复发率的最可能原因,并且在假设组织学上良性出现的周围性乳房组织的基因组正常时必须谨慎行事。本文的在线版本(doi:10.1007 / s10549-012-2290-3)包含补充材料,可供授权用户使用。

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