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:Contribution of MMP14-expressing cancer-associated fibroblasts in the tumor immune microenvironment to progression of colorectal cancer.
Contribution of MMP14-expressing cancer-associated fibroblasts in the tumor immune microenvironment to progression of colorectal cancer.
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基质金属蛋白酶14(MMP14)表达与结直肠癌进展相关,但其在肿瘤微环境(TME)中的作用尚不清楚。通过分析癌症基因组图谱中结直肠腺癌患者(n = 592)的转录组数据,探讨了MMP14与结直肠癌进展的相关性。通过对86例III期结直肠癌患者肿瘤样本的回顾性分析,采用12色多重免疫组化(mIHC)进行基于单细胞的空间MMP14表达谱分析,研究了MMP14在TME中的作用。基因表达数据分析显示,MMP14高表达与肿瘤进展相关,并提示癌症相关成纤维细胞(CAFs)和肿瘤相关巨噬细胞均参与该进展过程。mIHC空间分析显示,瘤内CAFs中MMP14+细胞比例较高(MMP14+ CAF/CAF比值)与较差的无复发生存期相关。纳入关键临床因素的多变量分析确定MMP14+ CAF/CAF比值为独立的不良预后因素。
此外,MMP14+ CAF/CAF比值高且TIL(肿瘤浸润淋巴细胞)密度低的患者亚组预后最差。我们的结果表明,MMP14+ CAFs在III期结直肠癌进展中发挥重要作用,因此可能是一个有前景的治疗靶点。
Matrix metalloproteinase 14 (MMP14) expression is implicated in progression of colorectal cancer, but its role in the tumor microenvironment (TME) has been unclear. The relevance of MMP14 to colorectal cancer progression was explored by analysis of transcriptomic data for colorectal adenocarcinoma patients ( n = 592) in The Cancer Genome Atlas. The role of MMP14 in the TME was investigated in a retrospective analysis of tumor samples from 86 individuals with stage III colorectal cancer by single cell-based spatial profiling of MMP14 expression as performed by 12-color multiplex immunohistochemistry (mIHC).
Analysis of gene expression data revealed that high MMP14 expression was associated with tumor progression and implicated both cancer-associated fibroblasts (CAFs) and tumor-associated macrophages in such progression. Spatial profiling by mIHC revealed that a higher percentage of MMP14 + cells among intratumoral CAFs (MMP14 + CAF/CAF ratio) was associated with poorer relapse-free survival. Multivariable analysis including key clinical factors identified the MMP14 + CAF/CAF ratio as an independent poor prognostic factor.
Moreover, the patient subset with both a high MMP14 + CAF/CAF ratio and a low tumor-infiltrating lymphocyte density showed the worst prognosis.
Our results suggest that MMP14 + CAFs play an important role in progression of stage III colorectal cancer and may therefore be a promising therapeutic target.
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