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:Tertiary lymphoid structures predict survival and response to neoadjuvant therapy in locally advanced rectal cancer.
Tertiary lymphoid structures predict survival and response to neoadjuvant therapy in locally advanced rectal cancer.
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三级淋巴结构(TLS)有助于抗肿瘤免疫反应,并可预测结直肠癌患者的预后。然而,TLS在塑造直肠腺癌免疫状态中的潜在影响,以及TLS与新辅助治疗(neoTx)之间的内在关系仍不清楚。
我们对221例接受neoTx治疗和242例未经治疗的局部晚期直肠癌(LARC)患者进行了苏木精-伊红染色、免疫组化和生物分子分析,以研究TLS和TIL(肿瘤浸润淋巴细胞)(TILs)。高TLS密度与无血管侵犯、较低的中性粒细胞与淋巴细胞比值、TLS成熟度增加、更长的无复发生存期(RFS)(风险比[HR] 0.2985,95%置信区间[CI] 0.1894-0.4706,p < 0.0001)以及适应性免疫细胞浸润增强显著相关。生物分子分析显示,高TLS评分与更多免疫细胞浸润和免疫相关通路激活增强密切相关。在neoTx队列中,治疗前标本中的TLS+肿瘤与TLS-肿瘤相比,与更高的良好缓解比例(62.5% vs. 29.8%,p < 0.0002)和病理完全缓解(pCR)(40.0% vs. 11.1%,p < 0.0001)相关,且RFS显著延长(HR 0.3574,95%CI 0.1489-0.8578,p = 0.0213),这一结果在GSE119409和GSE150082中得到证实。
进一步研究表明,neoTx显著降低了TLS密度和成熟度,并消除了TLS的预后价值。我们的研究表明,TLS可能在介导T细胞炎症性肿瘤微环境中发挥关键作用,这也为LARC患者的neoTx,尤其是新辅助免疫治疗提供了新方向。
Tertiary lymphoid structure (TLS) contributes to the anti-tumor immune response, and predicts the prognosis of colorectal cancer patients.
However, the potential impact of TLS in shaping the immune status of rectal adenocarcinoma, and the intrinsic relationship between TLS and neoadjuvant therapies (neoTx) remain unclear.
We performed hematoxylin-eosin staining, immunohistochemical and biomolecular analyses to investigate TLS and tumor-infiltrating lymphocytes (TILs) in 221 neoTx-treated and 242 treatment-naïve locally advanced rectal cancer (LARC) patients. High TLS density was significantly associated with the absence of vascular invasion, a lower neutrophil-to-lymphocyte ratio, increased TLS maturity, a longer recurrence-free survival (RFS) (hazard ratio [HR] 0. 2985 95% confidence interval [CI] 0. 1894-0. 4706, p < 0. 0001) and enhanced infiltration of adaptive immune cells.
Biomolecular analysis showed that high TLS-score was strongly associated with more infiltration of immune cells and increased activation of immune-related pathways. TLS + tumors in pre-treatment specimens were associated with a higher proportion of good respond (62. 5% vs. 29. 8%, p < 0. 0002) and pathological complete remission (pCR) (40. 0% vs. 11. 1%, p < 0. 0001), and significantly increased RFS (HR 0. 3574 95%CI 0. 1489-0. 8578 p = 0. 0213) compared with TLS - tumors in the neoTx cohort, which was confirmed in GSE119409 and GSE150082.
Further studies showed that neoTx significantly reduced TLS density and maturity, and abolished the prognostic value of TLS.
Our study illustrates that TLS may have a key role in mediating the T-cell-inflamed tumor microenvironment, which also provides a new direction for neoTx, especially neoadjuvant immunotherapy, in LRAC patients.
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