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HRAS 是乳腺恶性化疗耐药性腺肌上皮瘤的治疗靶点。

HRAS is a therapeutic target in malignant chemo-resistant adenomyoepithelioma of the breast.

机构信息

Genetics Department, Institut Curie, University of Paris, Paris, France.

Department of Diagnostic and Theranostic Medicine Paris, University of Paris, Paris, France.

出版信息

J Hematol Oncol. 2021 Sep 8;14(1):143. doi: 10.1186/s13045-021-01158-3.

Abstract

Malignant adenomyoepithelioma (AME) of the breast is an exceptionally rare form of breast cancer, with a significant metastatic potential. Chemotherapy has been used in the management of advanced AME patients, however the majority of treatments are not effective. Recent studies report recurrent mutations in the HRAS Q61 hotspot in small series of AMEs, but there are no preclinical or clinical data showing H-Ras protein as a potential therapeutic target in malignant AMEs. We performed targeted sequencing of tumours' samples from new series of 13 AMEs, including 9 benign and 4 malignant forms. Samples from the breast tumour and the matched axillary metastasis of one malignant HRAS mutated AME were engrafted and two patient-derived xenografts (PDX) were established that reproduced the typical AME morphology. The metastasis-derived PDX was treated in vivo by different chemotherapies and a combination of MEK and BRAF inhibitors (trametinib and dabrafenib). All malignant AMEs presented a recurrent mutation in the HRAS G13R or G12S hotspot. Mutation of PIK3CA were found in both benign and malignant AMEs, while AKT1 mutations were restricted to benign AMEs. Treatment of the PDX by the MEK inhibitor trametinib, resulted in a marked anti-tumor activity, in contrast to the BRAF inhibitor and the different chemotherapies that were ineffective. Overall, these findings further expand on the genetic features of AMEs and suggest that patients carrying advanced HRAS-mutated AMEs could potentially be treated with MEK inhibitors.

摘要

乳腺恶性腺肌上皮瘤(AME)是一种极为罕见的乳腺癌形式,具有显著的转移潜力。化疗已被用于治疗晚期 AME 患者,但大多数治疗方法并不有效。最近的研究报告了小系列 AME 中 HRAS Q61 热点的复发性突变,但没有临床前或临床数据表明 H-Ras 蛋白是恶性 AME 的潜在治疗靶点。我们对包括 9 例良性和 4 例恶性在内的 13 例 AME 的肿瘤样本进行了靶向测序。对一例恶性 HRAS 突变 AME 的乳腺肿瘤和腋窝转移的匹配样本进行了移植,并建立了 2 例患者来源的异种移植(PDX),这些异种移植再现了典型的 AME 形态。对转移衍生的 PDX 进行了不同化疗药物和 MEK 和 BRAF 抑制剂(曲美替尼和达拉非尼)联合治疗的体内治疗。所有恶性 AME 均存在 HRAS G13R 或 G12S 热点的复发性突变。在良性和恶性 AME 中均发现了 PIK3CA 突变,而 AKT1 突变仅限于良性 AME。MEK 抑制剂曲美替尼对 PDX 的治疗导致了明显的抗肿瘤活性,而 BRAF 抑制剂和不同的化疗药物则无效。总的来说,这些发现进一步扩展了 AME 的遗传特征,并表明携带晚期 HRAS 突变 AME 的患者可能可以用 MEK 抑制剂治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f17b/8424935/792c1e96f237/13045_2021_1158_Fig1_HTML.jpg

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