Li Zhongyang, Cai Shang, Li Huijun, Gu Jincheng, Tian Ye, Cao Jianping, Yu Dong, Tang Zaixiang
School of Radiation Medicine and Protection, Soochow University Medical College (SUMC), Suzhou, China.
Department of Radiotherapy and Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Front Oncol. 2021 Mar 9;11:622880. doi: 10.3389/fonc.2021.622880. eCollection 2021.
Lower-grade glioma (LGG) is a type of central nervous system tumor that includes WHO grade II and grade III gliomas. Despite developments in medical science and technology and the availability of several treatment options, the management of LGG warrants further research. Surgical treatment for LGG treatment poses a challenge owing to its often inaccessible locations in the brain. Although radiation therapy (RT) is the most important approach in this condition and offers more advantages compared to surgery and chemotherapy, it is associated with certain limitations. Responses can vary from individual to individual based on genetic differences. The relationship between non-coding RNA and the response to radiation therapy, especially at the molecular level, is still undefined.
In this study, using The Cancer Genome Atlas dataset and bioinformatics, the gene co-expression network that is involved in the response to radiation therapy in lower-grade gliomas was determined, and the ceRNA network of radiotherapy response was constructed based on three databases of RNA interaction. Next, survival analysis was performed for hub genes in the co-expression network, and the high-efficiency biomarkers that could predict the prognosis of patients with LGG undergoing radiotherapy was identified.
We found that some modules in the co-expression network were related to the radiotherapy responses in patients with LGG. Based on the genes in those modules and the three databases, we constructed a ceRNA network for the regulation of radiotherapy responses in LGG. We identified the hub genes and found that the long non-coding RNA, DRAIC, is a potential molecular biomarker to predict the prognosis of radiotherapy in LGG.
低级别胶质瘤(LGG)是一种中枢神经系统肿瘤,包括世界卫生组织(WHO)二级和三级胶质瘤。尽管医学科技有所发展且有多种治疗选择,但LGG的管理仍需进一步研究。LGG的手术治疗颇具挑战,因为其在大脑中的位置往往难以触及。虽然放射治疗(RT)是这种情况下最重要的方法,且与手术和化疗相比有更多优势,但它也存在一定局限性。基于基因差异,个体反应可能各不相同。非编码RNA与放射治疗反应之间的关系,尤其是在分子水平上,仍不明确。
在本研究中,利用癌症基因组图谱数据集和生物信息学,确定了低级别胶质瘤中参与放射治疗反应的基因共表达网络,并基于三个RNA相互作用数据库构建了放射治疗反应的ceRNA网络。接下来,对共表达网络中的枢纽基因进行生存分析,确定了可预测接受放射治疗的LGG患者预后的高效生物标志物。
我们发现共表达网络中的一些模块与LGG患者的放射治疗反应相关。基于这些模块中的基因和三个数据库,我们构建了一个用于调节LGG放射治疗反应的ceRNA网络。我们确定了枢纽基因,并发现长链非编码RNA DRAIC是预测LGG放射治疗预后的潜在分子生物标志物。