Pan Bo, Zhao Dongyi, Liu Yaqian, Li Na, Song Chen, Li Ning, Li Xuelu, Li Man, Zhao Zuowei
Department of Oncology & Department of Breast Surgery, The Second Hospital of Dalian Medical University, Dalian, 116023 China.
Department of Foreign Language, Dalian Medical University, Dalian, 116000 China.
Cancer Cell Int. 2020 Aug 3;20:365. doi: 10.1186/s12935-020-01459-6. eCollection 2020.
Mammary Paget's disease (MPD) is an uncommon cutaneous intraepithelial malignancy with ulceration of the nipple or areola. Its pathogenesis and genomic mutation remain largely unknown and no cell lines are established from primary tumors.
We collected surgical tumor specimens from a 65-year-old Chinese woman diagnosed with MPD and established patient-derived breast cancer (BC) organoids from MPD using organoid culture technology.
We successfully propagated BC organoids from a patient with MPD for more than 6 months. The organoids were cultured for long-term expansion without any change in spherical organoid morphology. Besides, the spherical organoid morphology did not change when they underwent cryopreservation after resuscitation. The H&E staining and immunohistochemistry analyses showed the similar morphological and histological features of the organoids compared with their paired original BC tissues. The organoids retained positive expression of breast cancer biomarkers: estrogen receptor, progesterone receptor, antigen Ki-67 and negative expression of human epidermal growth factor receptor 2. We also showed that MPD organoids recapitulated the unique genomic landscape including copy number alterations, mutational load, mutational signatures and cancer gene mutations by whole genome sequencing. In situ senescence-associated acid beta galactosidase assay confirmed senescence phenomenon existed in the process of organoids culture and there was no significant difference in the proportion of senescent organoids after organoid passage and resuscitation.
Our results suggested that an effective platform for ex vivo BC organoids from MPD patients could be used to explore clinicopathological and genomic characteristics of these patients.
乳腺佩吉特病(MPD)是一种罕见的伴有乳头或乳晕溃疡的皮肤上皮内恶性肿瘤。其发病机制和基因组突变在很大程度上仍不清楚,且尚未从原发性肿瘤中建立细胞系。
我们从一名65岁诊断为MPD的中国女性患者身上收集了手术肿瘤标本,并使用类器官培养技术从MPD中建立了患者来源的乳腺癌(BC)类器官。
我们成功地从一名MPD患者中培养出BC类器官超过6个月。类器官长期培养以进行扩增,其球形类器官形态没有任何变化。此外,复苏后进行冷冻保存时,球形类器官形态也没有改变。苏木精-伊红(H&E)染色和免疫组织化学分析显示,与配对的原始BC组织相比,类器官具有相似的形态和组织学特征。类器官保留了乳腺癌生物标志物的阳性表达:雌激素受体、孕激素受体、抗原Ki-67,以及人表皮生长因子受体2的阴性表达。我们还通过全基因组测序表明,MPD类器官重现了独特的基因组格局,包括拷贝数改变、突变负荷、突变特征和癌症基因突变。原位衰老相关酸性β半乳糖苷酶检测证实类器官培养过程中存在衰老现象,类器官传代和复苏后衰老类器官的比例没有显著差异。
我们的结果表明,一个来自MPD患者的离体BC类器官有效平台可用于探索这些患者的临床病理和基因组特征。