RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Increased CD56 expression after photodynamic therapy indicates an increased natural killer cell count following early photodynamic therapy for cutaneous squamous cell carcinoma.
Increased CD56 expression after photodynamic therapy indicates an increased natural killer cell count following early photodynamic therapy for cutaneous squamous cell carcinoma.
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皮肤鳞状细胞癌(cSCC)是第二常见的皮肤癌类型。光动力疗法(PDT)是一种有前景的cSCC治疗方法,因为它已被证明能够随时间靶向特定区域,且副作用风险低。PDT可能导致组织损伤和血管关闭,并可能调节局部免疫反应。
本研究旨在探讨和比较SCC进行PDT前后的早期淋巴细胞变化。通过病理检查共识别出10例SCC患者。最初,所有创面均以20%氨基乙酰丙酸(ALA)-PDT作为治疗过程的第一阶段进行处理。创面通过暴露于波长为635 nm、能量密度为100 J/cm²、强度为80 mW/cm²的红色LED光进行处理。24小时后手术切除肿瘤组织,并再次进行一轮PDT治疗。对术后创面组织进行CD3和CD56的免疫组化检测。如果创面出现肉芽、坏死或分泌物,则在治疗中加入清创术。所有患者治疗后随访0.6-1.0年。ALA-PDT联合手术完全控制了全部10例患者的肿瘤组织。创面组织的免疫组化分析显示,光动力治疗后CD56表达增加,而CD3表达无差异。这些结果也间接表明,10例患者中NK细胞总数增加,但T淋巴细胞计数无变化。
总之,ALA-PDT联合手术治疗cSCC显示出良好效果。CD56表达增加可能是PDT有效治疗cSCC的一种机制。
Cutaneous squamous cell carcinoma (cSCC) is the second most common type of skin cancer. Photodynamic therapy (PDT) is a promising therapeutic method for managing cSCC due to its proven ability to target specific areas over time and its low risk of side effects. PDT may cause tissue damage and vascular shutdown, and may regulate local immunological responses. The present study aimed to investigate and compare the early lymphocyte modifications before and after PDT for SCC. A total of 10 patients with SCC were identified by pathological investigation. Initially, all wounds were treated with 20% aminolevulinic acid (ALA)-PDT as the initial stage in the therapeutic procedure. The wounds were treated by exposing them to red LED light with a wavelength of 635 nm, an energy density of 100 J/cm 2 and an intensity of 80 mW/cm 2 .
The tumor tissue was surgically removed 24 h later, and another round of PDT therapy was administered. Immunohistochemistry for CD3 and CD56 was conducted on the wound tissue post-surgery. If the wound showed granulation, necrosis or secretion, debridement was added to the therapy. All patients were monitored for 0. 6-1. 0 year post-treatment.
ALA-PDT combination surgery fully controlled the tumor tissue in all 10 patients. The immunohistochemical analysis of the wound tissues showed that the expression of CD56 increased, while the expression of CD3 was not different after photodynamic therapy. These results also indirectly indicated that the overall count of NK cells in the 10 patients increased, nevertheless, there was no alteration in the T lymphocyte count.
In conclusion, the ALA-PDT combination surgical therapy for cSCC demonstrates favorable results. An increase in CD56 expression may be a mechanism for the effective treatment of cSCC with PDT.
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