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首页> 外文期刊>The breast journal >Invasive breast carcinomas with ATM ATM ATM gene variants of uncertain significance share distinct histopathologic features
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Invasive breast carcinomas with ATM ATM ATM gene variants of uncertain significance share distinct histopathologic features

机译:侵入性乳房癌与ATM ATM ATM基因变异不确定意义份额份异明显的组织病理学特征

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Abstract The increasing availability of next‐generation sequencing for clinical research dramatically improved our understanding of breast cancer genetics and resulted in detection of new mutation variants. Cancer risk data relating to some of these variants are insufficient, prompting the designation of variants of uncertain significance (VUS). The histopathologic characteristics of these variants have not been previously described. We propose to depict these characteristics and determine if invasive carcinomas with similar VUS genes share similar histomorphologic features. In total, 28 invasive breast cancers with VUS were retrospectively identified. Tumor sections were reviewed and a predefined set of histopathologic characteristics were documented and compared. Nine of the 28 cases were variants in the ATM gene and were found to share similar histologic characteristics; all had tumor cells with low nuclear grade, absent tumor infiltrating lymphocytes, as well as a marked desmoplastic response. A subset of the above findings were identified in variants of other genes but none had all findings collectively. Furthermore, variants of ATM gene had smaller tumor size, lower pathologic T stage at presentation, and more favorable surrogate molecular subtype compared to variants of other genes. These findings could potentially be used to reclassify VUS and predict which patients may harbor ATM mutations, and hence could have implications in triaging toward ATM variant identification for potential future targeted therapy.
机译:摘要对临床研究的下一代测序的越来越多的可用性大大提高了我们对乳腺癌遗传学的理解,并导致检测新的突变变体。与这些变体有关的癌症风险数据不足,促使指定不确定意义(VUS)的变体。尚未描述这些变体的组织病理学特征。我们建议描绘这些特征,并确定具有类似VUS基因的侵入性癌是否共享类似的组织特征。总共有28个具有VUS的侵袭性乳腺癌,回顾性地确定。综述肿瘤切片并记录了预定义的组织病理学特征并进行了比较。 28例中的九个患者是ATM基因的变体,发现共享相似的组织学特征;所有患有低核等级的肿瘤细胞,不存在肿瘤浸润淋巴细胞,以及标记的去制剂反应。在其他基因的变体中鉴定了上述结果的副本,但没有共同发现所有结果。此外,ATM基因的变体具有较小的肿瘤大小,呈递较低的病理T阶段,与其他基因的变体相比,更有利的替代分子亚型。这些发现可能用于重新分类VUS和预测哪些患者可能涉及ATM突变,因此可能对TRIA引起的TIAIAG识别潜在未来的靶向治疗。

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