[乳腺癌 HER2 mRNA 定量分析与 HER2 免疫组化 0]。

M C Sun, S F Wu, Y M Cai, Y Y Liu, K M Li, D C Zhao, X Zeng
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引用次数: 0

摘要

目的通过HER2免疫组化(IHC)0检测乳腺癌中HER2 mRNA的表达,并初步分析通过HER2 mRNA水平区分HER2μ超低表达肿瘤和HER2无表达肿瘤(IHC无染色)的可行性。方法:采用逆转录数字 PCR 技术对北京协和医院于 2020 年 1 月至 2023 年 3 月间获得的 41 例福尔马林固定石蜡包埋的浸润性乳腺癌手术组织样本进行 HER2 mRNA 分析。样本中包括 21 例 HER2 IHC 1+ 和 20 例 IHC 0(12 例超低表达,8 例未表达 HER2)。HER2 mRNA表达水平通过FAM(HER2)/VIC(参考基因)比值进行定量评估。结果经IHC检测HER2 mRNA表达量为1+、超低和不表达的病例的HER2 mRNA表达量分别为0.30至1.78(平均0.90,中位0.82)、0.55至1.51(平均0.93,中位0.90)和0.22至0.78(平均0.41,中位0.36)。在 HER2 mRNA 平均水平和中位数方面,HER2 IHC 1+ 和 HER2 超低表达疾病之间无显著差异(P=0.757)。而 HER2 IHC 1+ 和 HER2 未表达的肿瘤之间的 HER2 基因表达存在明显差异(P=0.002)。而且,通过 IHC 检测,HER2 超低病例的 HER2 mRNA 含量高于 HER2 未表达亚组(P=0.001)。结论根据 HER2 mRNA,HER2 不表达和 HER2 弱表达(包括 HER2 IHC 1+ 和超低表达)属于两种不同类型的肿瘤,HER2 IHC 1+ 和 HER2 超低表达的疾病可能是相同的。有必要进一步测试 HER2 mRNA 检测对 HER2 弱表达亚组分层的性能,并确定阈值。
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[Quantitative HER2 mRNA assay in breast cancer with HER2 immunohistochemistry 0].

Objective: To investigate HER2 mRNA expression in breast cancer with HER2 immunohistochemistry (IHC) 0 and to analyze the feasibility of distinguishing between the tumor with HER2 μltra-low expression and the one without expression of HER2 (no staining by IHC) by HER2 mRNA level preliminarily. Methods: HER2 mRNA was analyzed by reverse transcription digital PCR in 41 cases of formalin-fixed paraffin-embedded surgical tissue samples of invasive breast cancer obtained between January 2020 and March 2023 at Peking Union Medical College Hospital. The cohort included 21 HER2 IHC 1+ and 20 IHC 0 (12 ultra-low and 8 non-expression of HER2). HER2 mRNA expression level was quantitatively evaluated by the FAM (HER2)/VIC (reference gene) ratio. Results: The expression of HER2 mRNA for the cases with 1+, ultra-low, and non-expression of HER2 by IHC was 0.30 to 1.78 (average 0.90, median 0.82), 0.55 to 1.51 (average 0.93, median 0.90) and 0.22 to 0.78 (average 0.41, median 0.36), respectively. For the mean and median HER2 mRNA levels, there was no significant difference between HER2 IHC 1+ and HER2 ultra-low expression diseases (P=0.757). A remarkable difference in HER2 gene expression was found between the tumors with 1+ and non-expression of HER2 by IHC (P=0.002). And, HER2 ultra-low cases contained statistically higher levels of HER2 mRNA compared with non-expression of HER2 subgroup by IHC (P=0.001). Conclusions: Based on HER2 mRNA, HER2 non-expression and HER2 weak expression (including HER2 IHC 1+ and ultra-low) belong to two different types of the tumor and the disease with HER2 IHC 1+ and HER2 ultra-low expression may be the same. It is necessary to further test the performance of HER2 mRNA detection for stratifying the HER2 weak expression subgroup and to determine the threshold.

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来源期刊
中华病理学杂志
中华病理学杂志 Medicine-Medicine (all)
CiteScore
1.00
自引率
0.00%
发文量
10377
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[Advances in pathological diagnostic scoring systems and specific immune markers of adrenocortical carcinoma]. [Angiomatosis of the breast: a clinicopathological analysis of six cases]. [Application value of immunohistochemistry INSM1 combined with periodic acid-Schiff stain double staining in glandular and neuroendocrine amphicrine carcinoma in the digestive tract]. [Biological characteristics of triple negative breast cancer with low expression of HER2]. [Brenner tumor of the vagina: report of a case].
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