基于 DNA 超分子水凝胶的保护性 NK 细胞储库用于增强三阴性乳腺癌治疗
Protective NK Cell Reservoir Based on DNA Supramolecular Hydrogel for Enhanced Triple-Negative Breast Cancer Therapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Comparative morphology of tumour microenvironment in claudin-low and claudin-high breast cancers.
Comparative morphology of tumour microenvironment in claudin-low and claudin-high breast cancers.
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上述基于形态学的研究揭示,与 claudin-high 肿瘤相比,claudin-low 肿瘤具有独特的免疫和非免疫 TME。未来探索上述每种形态学特征分子关联的研究,有助于识别治疗 claudin-low BCs 的新治疗靶点。
Claudin-low型乳腺癌(BC)比claudin-high型表现出更具侵袭性的行为。Claudin-low型BC通常以更高分级、干性特征富集以及转移倾向等特征为特点。肿瘤微环境(TME)被定义为由周围细胞、血管和细胞外基质成分构成的复杂网络,它影响乳腺组织内癌细胞的行为。理解TME对于认识claudin-low型BC的侵袭性特征至关重要。
在本研究中,我们利用15例claudin-low和12例claudin-high BC组织样本的H&E染色切片,研究了免疫和非免疫TME的形态学。
观察到claudin-low型BCs的TME中,收缩裂隙(66.6%;n = 10/15)、不成熟促纤维增生反应(40%;n = 6/15)、较高的间质细胞密度(60%;n = 9/15)以及成纤维细胞增殖(53.3%;n = 8/15)的发生频率显著更高,而弹性组织变性(66.6%;n = 10/15)的发生率较低。免疫微环境显示,其中总TILs(80%;n = 12/15)以及间质TILs(86.67%;n = 13/15)和瘤内TILs(60%;n = 9/15)的发生频率更高。
Claudin-low breast cancers (BCs) exhibit more aggressive behaviour compared to claudin-high types. Claudin-low BCs are often characterized by features such as a higher grade, enrichment of stemness characteristics, and a propensity for metastasis. Tumour microenvironment (TME) defined as the intricate network of surrounding cells, blood vessels, and extracellular matrix components influences the behaviour of cancer cells within the breast tissue. Understanding the TME is crucial for comprehending the aggressive characteristics of claudin-low BCs.
In this study, we have studied the morphology of immune and non-immune TME using Haematoxylin and eosin (H&E)-stained slides of 15 claudin-low and 12 claudin-high tissue samples of BC.
TME of claudin-low BCs was observed to have a significantly higher frequency of retraction clefts (66.6 %; n = 10/15), immature desmoplastic response (40 %; n = 6/15), higher stromal cellularity (60 %; n = 9/15); and fibroblastic proliferation (53.3 %; n = 8/15) with a low prevalence of elastosis (66.6 %; n = 10/15). The immune microenvironment revealed a higher frequency of total (80 %; n = 12/15) as well as stromal (86.67 %; n = 13/15) and intra-tumoural TILs (60 %; n = 9/15) in them.
The above morphology-based study revealed that claudin-low tumours have unique immune and non-immune TME as compared to claudin-high tumours. Future studies exploring the molecular correlates of each of the above morphological features can help in identifying novel therapeutic targets for the treatment of claudin-low BCs.
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