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:Tendomodulin in pan-cancer analysis: exploring its impact on immune modulation and uncovering functional insights in colorectal cancer.
Tendomodulin in pan-cancer analysis: exploring its impact on immune modulation and uncovering functional insights in colorectal cancer.
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我们的研究结果揭示了 TNMD 在 CRC 中关键的免疫调节作用,尤其是在影响肿瘤-免疫相互作用方面。除了作为潜在的诊断和预后生物标志物外,TNMD 还促进 CRC 的转移和侵袭,因此成为一个有前景的治疗靶点。这些发现突显了 TNMD 在 CRC 以及可能其他恶性肿瘤中的重要性。
Tendomodulin (TNMD) 在多种恶性肿瘤中起关键作用,包括结直肠癌 (CRC)。然而,其在不同癌症中的全面影响,尤其是在 CRC 中的免疫调节功能,仍未得到充分探索。本研究通过综合分子和临床分析,聚焦 TNMD 的免疫调节功能,探讨其在 CRC 中的作用。
利用多个生物信息学数据库和分析工具对TNMD进行泛癌分析。为验证TNMD在CRC中的作用,我们进行了包括免疫荧光(IF)、免疫组织化学(IHC)、实时定量逆转录PCR(qPCR)、western blotting和细胞迁移实验在内的实验。
TNMD表达和基因突变在不同癌症中存在差异,并具有较高的诊断价值。生存分析发现,TNMD与多种癌症的预后相关。值得注意的是,在高度微卫星不稳定(MSI-H)CRC患者中,TNMD表达与多种免疫细胞呈正相关,尤其是自然杀伤(NK)细胞,而与调节性T细胞(Tregs)呈负相关。至关重要的是,在微卫星稳定(MSS)CRC患者中,高TNMD表达与更好的免疫治疗结局相关,表明其有潜力作为患者分层和个体化治疗策略的生物标志物。此外,单细胞测序数据显示,在肿瘤微环境中,TNMD阳性肿瘤细胞与成纤维细胞或巨噬细胞之间的相互作用更强。最后,TNMD在CRC肿瘤组织和细胞系中过表达,从而促进侵袭和转移。
Tendomodulin (TNMD) is pivotal in various malignancies, including colorectal cancer (CRC). However, its comprehensive impact across cancers, particularly its immunomodulatory function in CRC, remains underexplored. This study explored the role of TNMD in CRC by focusing on its immunomodulatory functions through comprehensive molecular and clinical analyses.
Multiple bioinformatics databases and analytical tools were utilized for the TNMD in pan-cancer analysis. To validate the role of TNMD in CRC, we performed experiments, including immunofluorescence (IF), immunohistochemistry (IHC), real-time quantitative reverse transcription PCR (qPCR), western blotting, and cell migration assays.
TNMD expression and gene mutation vary across cancers and offer high diagnostic value. Survival analysis found that TNMD is associated with prognosis in multiple cancers. Notably, in patients with high microsatellite instability (MSI-H) CRC, TNMD expression correlated positively with various immune cells, particularly natural killer (NK) cells, whereas it was inversely correlated with regulatory T cells (Tregs). Crucially, in patients with microsatellite stability (MSS) CRC, high TNMD expression was associated with better immunotherapy outcomes, indicating its potential as a biomarker for patient stratification and tailored treatment approaches. Furthermore, single-cell sequencing data revealed stronger interactions between TNMD-positive tumor cells and fibroblasts or macrophages in the tumor microenvironment. Finally, TNMD was overexpressed in CRC tumor tissues and cell lines, thereby promoting invasion and metastasis.
Our findings reveal a critical immunomodulatory role of TNMD in CRC, particularly in influencing tumor-immune interactions. Beyond its potential diagnostic and prognostic biomarker, TNMD promotes CRC metastasis and invasion, thus emerging as a promising therapeutic target. These findings highlight TNMD's significance in CRC and potentially other malignancies.
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