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DNA损伤修复基因突变表明免疫检查点抑制剂治疗的结直肠癌预后良好。

DNA Damage Repair Gene Mutations Are Indicative of a Favorable Prognosis in Colorectal Cancer Treated With Immune Checkpoint Inhibitors.

作者信息

Song Yipeng, Huang Jian, Liang Dandan, Hu Ying, Mao Beibei, Li Qiujing, Sun Huaibo, Yang Ying, Zhang Jiao, Zhang Henghui, Chen Huan, Liu Hao, Zhang Shukun

机构信息

Department of Radiation Oncology, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, China.

Institute of Oncology, First Affiliated Hospital of Kunming Medical University, Kunming, China.

出版信息

Front Oncol. 2021 Feb 19;10:549777. doi: 10.3389/fonc.2020.549777. eCollection 2020.

Abstract

BACKGROUND

DNA damage repair (DDR) genes were recently implicated in the anti-tumor immune response. Therefore, it is worthwhile to unravel the implications of DDR pathways in the shaping of immune responsiveness in colorectal cancer (CRC) patients receiving immune checkpoint inhibitors (ICI).

METHODS

We analyzed publicly available genomic data from a cohort treated with ICI from Memorial Sloan Kettering Cancer Center (MSK ICI cohort). To characterize the impact of the DDR mutation, the genomic data of The Cancer Genome Atlas (TCGA) colorectal adenocarcinoma (COADREAD) dataset was explored. We also analyzed the incidence of DDR mutation and microsatellite instability-high (MSI-H) in a Chinese CRC cohort using panel sequencing.

RESULTS

The DDR pathway was commonly mutated (21.8%) in the multicancer MSK ICI cohort, with the highest frequency of 36.4% in CRCs. Survival analysis showed that DDR mutation correlated with an improved overall survival (OS) in CRCs and pan-cancer in the MSK ICI cohort. However, no significant associations were identified in the TCGA COADREAD and MSK non-ICI CRCs. DDR mutation was associated with higher tumor mutational burden (TMB) levels and increased immune cell infiltration and immune checkpoint molecule expression in the TCGA COADREAD dataset. Last, we investigated the DDR mutational pattern and its associations with MSI-H and other genomic features in a Chinese CRC cohort. Notably, MSI-H and DDR mutation was present in 5.7% and 13.4% of cases, respectively, which suggests that DDR identifies a higher proportion of potential responders than MSI-H.

CONCLUSION

Our data suggest that DDR mutation as an indication of enhanced cancer immunity, and it may function as a biomarker for patients with CRCs receiving ICI treatment. The high incidence of DDR mutation in the Chinese CRC cohort emphasizes the future utility of panel-based DDR evaluation in guiding ICI treatment.

摘要

背景

DNA损伤修复(DDR)基因最近被认为与抗肿瘤免疫反应有关。因此,有必要阐明DDR通路在接受免疫检查点抑制剂(ICI)治疗的结直肠癌(CRC)患者免疫反应形成中的作用。

方法

我们分析了纪念斯隆凯特琳癌症中心(MSK ICI队列)接受ICI治疗的一组患者的公开基因组数据。为了表征DDR突变的影响,我们探索了癌症基因组图谱(TCGA)结直肠腺癌(COADREAD)数据集的基因组数据。我们还使用靶向测序分析了中国CRC队列中DDR突变和微卫星高度不稳定(MSI-H)的发生率。

结果

在多癌种MSK ICI队列中,DDR通路普遍发生突变(21.8%),在CRC中的突变频率最高,为36.4%。生存分析表明,在MSK ICI队列中,DDR突变与CRC和泛癌患者的总生存期(OS)改善相关。然而,在TCGA COADREAD和MSK非ICI CRC患者中未发现显著关联。在TCGA COADREAD数据集中,DDR突变与更高的肿瘤突变负荷(TMB)水平、增加的免疫细胞浸润和免疫检查点分子表达相关。最后,我们在中国CRC队列中研究了DDR突变模式及其与MSI-H和其他基因组特征的关联。值得注意的是,MSI-H和DDR突变分别出现在5.7%和13.4%的病例中,这表明DDR比MSI-H识别出更高比例的潜在反应者。

结论

我们的数据表明,DDR突变表明癌症免疫增强,它可能作为接受ICI治疗的CRC患者的生物标志物。中国CRC队列中DDR突变的高发生率强调了基于靶向测序的DDR评估在指导ICI治疗方面的未来实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f503/7934780/91d38d7eff4c/fonc-10-549777-g001.jpg

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