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:Clinicopathological Significances and Prognostic Role of Intratumoral Budding in Colorectal Cancers.
Clinicopathological Significances and Prognostic Role of Intratumoral Budding in Colorectal Cancers.
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ITB 与 CRC 的侵袭性肿瘤行为和更差的预后显著相关。作为一种组织学参数,ITB 的检测可用于预测 CRC 的临床病理特征和预后。
本研究旨在通过meta分析评估结直肠癌(CRC)中肿瘤出芽(ITB)的临床病理意义及预后价值。
我们使用13项符合条件的研究进行了meta分析,并调查了高ITB的CRC发生率。评估了ITB与临床病理特征(包括无病生存期)之间的相关性。
在总体CRC中,高ITB的估计率为0.233(95%置信区间(CI)0.177-0.299)。高ITB与肿瘤分级、淋巴管侵犯、神经周围侵犯、pT分期和淋巴结转移显著相关。此外,ITB在髓样癌和印戒细胞癌中比在传统腺癌和黏液癌中更常见。然而,高ITB率与肿瘤边界、TIL(肿瘤浸润淋巴细胞)或微卫星不稳定性无关。新辅助治疗后反应良好的CRC显示高ITB率低于反应差者(风险比(HR)0.114,95% CI 0.070-0.179 vs. 0.321,95% CI 0.204-0.467)。此外,高ITB的CRC无病生存期低于低ITB者(HR 1.426,95% CI 1.092-1.863)。
This study aims to evaluate the clinicopathological significance and prognostic implications of intratumoral budding (ITB) in colorectal cancers (CRCs) through a meta-analysis.
We performed the meta-analysis using 13 eligible studies and investigated the rates of CRCs with high ITB. The correlation between ITB and clinicopathological characteristics, including disease-free survival, was evaluated.
The estimated rate of CRCs with high ITB was 0.233 (95% confidence interval (CI) 0.177-0.299) in overall CRCs. High ITB was significantly correlated with tumor grade, lymphatic invasion, perineural invasion, pT stage, and lymph node metastasis. In addition, ITBs were more frequently found in medullary and signet-ring cell carcinomas than in conventional adenocarcinomas and mucinous carcinomas. However, the high ITB rate was not correlated with tumor border, tumor-infiltrating lymphocytes, or microsatellite instability. CRCs with a good response after neoadjuvant therapy revealed a lower rate of high ITB than those with a poor response (hazard ratio (HR) 0.114, 95% CI 0.070-0.179 vs. 0.321, 95% CI 0.204-0.467). In addition, CRCs with high ITB had a worse disease-free survival than those with low ITB (HR 1.426, 95% CI 1.092-1.863).
The ITB was significantly correlated with aggressive tumor behaviors and a worse prognosis in CRCs. The detection of ITB, as a histological parameter, can be useful for predicting clinicopathologic features and the prognosis of CRC.
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