CD81 通过阻断 CD274/PD-L1 的选择性自噬降解驱动放射抵抗性胶质母细胞瘤的免疫逃逸
CD81 drives immune evasion in radioresistant glioblastoma by blocking selective autophagic degradation of CD274/PD-L1.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Inside the Tumor: Decoding the Feline Mammary Tumor Microenvironment and Its Prognostic Value-A Review.
Inside the Tumor: Decoding the Feline Mammary Tumor Microenvironment and Its Prognostic Value-A Review.
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肿瘤微环境(TME)由肿瘤细胞、基质细胞及细胞外基质成分组成,它们之间复杂的相互作用最终决定了肿瘤发生、癌症进展及治疗反应。尽管在人类肿瘤学领域已对TME进行了广泛研究,但关于其兽医对应物,尤其是猫乳腺肿瘤(FMTs)的数据仍然稀缺。在本综述中,我们探讨了目前对猫乳腺癌(FMC)微环境的理解,重点关注肿瘤坏死、纤维化、血管生成、脂肪组织肿瘤相关炎症、细胞外囊泡以及上皮-间质转化(EMT)及其预后意义。在FMC中,胶原纤维重塑、癌症相关成纤维细胞(CAFs)、调节性T细胞(Tregs)和血清瘦素水平升高与不良预后相关,而基质细胞毒性T细胞则与更有利的结局相关。相比之下,关于坏死和促血管生成因子的研究结果仍不一致,对细胞外囊泡(EVs)的研究仍处于早期阶段。本综述呈现了来自人类乳腺癌(HBC)的见解,进一步支持并阐明了这些TME组分的潜在相关性。由于FMC是高度侵袭性的肿瘤,对其微环境的深入理解不仅能够提高预后准确性,还能揭示新的治疗靶点。
此外,由于二者之间的相似性,FMC为HBC提供了一个潜在有价值的自发模型,特别是对于侵袭性三阴性表型。
The tumor microenvironment (TME) comprises neoplastic and stromal cells, and extracellular matrix elements, all engaging in a complex interplay that ultimately dictates tumorigenesis, cancer progression, and therapeutic response. While extensive research on the TME has been conducted in human oncology, data on its veterinary counterpart, particularly in feline mammary tumors (FMTs), are still scarce. In this review, we explore current understanding of feline mammary carcinoma (FMC) microenvironment, focusing on tumor necrosis, fibrosis, angiogenesis, adipose tissue tumor-associated inflammation, extracellular vesicles, and epithelial-mesenchymal transition (EMT) and their prognostic implications.
In FMC, remodeling of collagen fibers, cancer-associated fibroblasts (CAFs), regulatory T cells (Tregs) and elevated serum leptin have been associated with poor prognosis, whereas stromal cytotoxic T cells correlate with more favorable outcomes. By contrast, findings on necrosis and pro-angiogenic factors remain inconsistent, and research on extracellular vesicles (EVs) is still in its early stages.
This review presents insights from human breast cancer (HBC) that further support and elucidate the potential relevance of these TME components. As FMCs are highly aggressive tumors, a deeper understanding of their microenvironment could not only improve prognostic accuracy but also uncover novel therapeutic targets.
Furthermore, due to their similarities, FMCs offer a potential valuable spontaneous model for HBC, particularly for the aggressive triple-negative phenotypes.
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