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:Galectin-1-Targeted Type-I/II Photosensitizers Activate the NF-κB Pathway to Enhance Immunity and Treat High-Risk HPV-Associated Cervical Lesions.
Galectin-1-Targeted Type-I/II Photosensitizers Activate the NF-κB Pathway to Enhance Immunity and Treat High-Risk HPV-Associated Cervical Lesions.
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女性持续感染高危型HPV可进展为宫颈上皮内瘤变,甚至宫颈癌。本研究考察TBTCN-TDG光动力治疗(PDT)探针治疗HPV相关宫颈病变时的细胞毒和免疫调节作用。该探针将供体-受体-π-受体1(D-A-π-A1)结构(TBTCN)与靶向半乳糖凝集素-1的TDG基团结合,并在HPV阳性SiHa细胞中确认其靶向能力。体外结果显示,TBTCN-TDG联合光照显著抑制SiHa细胞增殖、增加凋亡,并通过增强NF-κB通路信号刺激树突状细胞、巨噬细胞和NK细胞,从而激活免疫应答。体内激光照射下,该靶向光敏剂表现出显著治疗效果;TUNEL染色显示病灶凋亡增加。免疫分析表明,激光照射下TBTCN-TDG提高NK细胞活性,并增加TNF-α、IFN-γ和IL-6等促炎细胞因子水平,证实免疫应答被激活。
总之,TBTCN-TDG联合PDT可有效靶向HPV感染细胞、增强免疫应答并抑制HPV感染,提示其可能成为治疗高危型HPV感染患者的光动力免疫新策略。
Persistent infection with high-risk HPV in women can progress to cervical intraepithelial neoplasia and even cervical cancer.
This study investigated the cytotoxic and immunomodulatory effects of the TBTCN-TDG photodynamic therapy (PDT) probe in treating HPV-associated cervical lesions. The TBTCN-TDG probe was designed by integrating a donor-acceptor- -acceptor 1 (D-A- -A1) structure (TBTCN) with TDG, a moiety targeting Galectin-1, and its targeting ability in HPV-positive SiHa cells was confirmed. The in vitro results demonstrated that TBTCN-TDG combined with light treatment significantly inhibited SiHa cell proliferation, increased apoptosis, and activated immune responses by stimulating dendritic cells, macrophages, and NK cells, through enhanced NF- B pathway signaling.
In vivo, this targeted photosensitizer exhibited substantial therapeutic effects under laser excitation, as evidenced by TUNEL staining, which showed increased apoptosis in lesions. Immune analysis indicated that TBTCN-TDG enhanced NK cell viability and elevated the levels of pro-inflammatory cytokines under laser excitation, such as TNF- , IFN- , and IL-6, confirming immune response activation.
In conclusion, the combination of TBTCN-TDG and PDT effectively targets cells infected with HPV, enhances immune responses, and suppresses HPV infection. This suggests a novel therapeutic strategy for photodynamic immunotherapy in patients with cervical high-risk HPV infections.
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