双相 (状) 乳头性细胞癌:在PRCC谱中是一个独特的分子和形态亚型
Zhichun Lu1, Yan Zhou2, Wei Fan2
1Department of Pathology & Laboratory Medicine, Boston Medical Center, Boston University Chobanian & Avedisian School of Medicine, 670 Albany St., Boston, MA, 02118, USA. zhichun.lu@bmc.org.
Virchows Archiv : an international journal of pathology
|September 27, 2025
概括
双相 (状) 乳头性细胞癌 (BPRCC) 是一种独特的癌亚型. 分子分析揭示了独特的NOTCH,MAPK和DNA修复途径的改变,支持其作为一个独立实体的分类.
科学领域:
- 在瘤学瘤学.
- 脏病理学 脏病理学
- 分子诊断学 分子诊断
背景情况:
- 双相 (状) 乳头性细胞癌 (BPRCC) 是一种罕见的细胞癌变体.
- 它独特的临床病理学和分子特征需要进一步探索.
研究的目的:
- 描述BPRCC的组织学,免疫类型,分子和临床特征.
- 为了确定BPRCC是否代表了斑纹性细胞癌的独特亚型.
主要方法:
- 对十例BPRCC病例的组织学和免疫类型分析.
- 在染色体异常的情况下进行光在位杂交 (FISH).
- 下一代测序 (NGS) 用于针对基因突变和放大.
主要成果:
- 所有十个BPRCC瘤都表现出双相形态,并被分为pT1.1.
- 免疫组织化学显示PAX8,CK7,AMACR和Claudin4的扩散阳性,细胞群之间的表达差异.
- 在所有病例中,FISH证实了三发症7和17. 在90%的病例中,NGS发现了NOTCH1突变,30%的MET改变,以及DDR和染色体重塑基因的改变.
结论:
- BPRCC是一种独特的状细胞癌亚型,其特征是双相形态和特定的免疫表型标记.
- 对于NOTCH,MAPK和DNA损伤反应 (DDR) 途径的改变,BPRCC的分子概况得到了丰富.
- 在研究的队列中,BPRCC显示了有利的临床结果,没有观察到疾病进展或与癌症相关的死亡.
相关概念视频
Abnormal Proliferation
5.1K
Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the...
5.1K
The Retinoblastoma Gene
4.7K
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
4.7K


