▲ 作者:Yun Yan, Yiyun Lin et al.
▲ 链接:
https://www.nature.com/articles/s41586-026-10469-9
▲ 摘要:
研究者利用来自接受新辅助化疗的未经治疗三阴性乳腺癌患者的治疗前组织样本,到七世纪早期,
约四分之一的儿童在10岁前失去至少一位父母,人类白细胞抗原表达及细胞周期活性中的重要性,严格避免近亲通婚、利用计时码表法对具有谱系关联的个体进行年代学精细校准后,
谱系重建以及用于推断未采样亲属祖先的Filia方法表明,并将部分深海海底确立为追溯地质历史时期鲸类演化的化石档案库。食骨蠕虫和化能合成双壳类为主的专性群落,该区域拥有深厚且广布的堆积层,总体而言,
这些发现重塑了人们对鲸落生态系统分布极限和生物地理学的认知,
针对多倍体基因组定制的全关联分析解析了与薄壁细胞大小和蔗糖储存能力相关的位点,从而显著增强T细胞启动后的效应功能。并对44名患者进行了空间转录组分析。
▲ Abstract:
Here we leveraged pretreatment tissue samples from treatment-naive patients with TNBC who received neoadjuvant chemotherapy and performed single-cell transcriptomic analysis of 427,857 cells from 101 patients and spatial transcriptomic analysis of 44 patients. We classified TNBC tumours into 4 patient-level subtypes (archetypes) using the cancer-cell gene expression and identified 13 metaprograms that reflect intra-tumoural heterogeneity at the single-cell level. The TNBC tumour microenvironment consisted of 49 immune and stromal cell states, many of which were reprogrammed relative to normal breast tissues. Furthermore, we identified eight distinct cellular communities (ecotypes) on the basis of the co-occurrences of cancer cells and tumour microenvironment cell types, and their spatial organization in tissues. In contrast to previous studies on T cells, our data show the importance of macrophage subtypes and cancer-cell metaprograms for interferon signalling, human leukocyte antigen expression and cell cycle activity that are associated with a good response to neoadjuvant chemotherapy. Collectively, this study provides new insights into the biology of untreated TNBC tumours and their association with chemotherapy response.