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Autophagy-related lncRNA and its related mechanism in colon adenocarcinoma
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作者 Feifei Tan Zhongyin Zhou 《Oncology and Translational Medicine》 CAS 2021年第6期305-313,共9页
Objective Colon cancer is a type of cancer with high morbidity and mortality,of which adenocarcinoma is the most common type.Numerous studies have found that long noncoding RNAs(lncRNAs)are related to the occurrence a... Objective Colon cancer is a type of cancer with high morbidity and mortality,of which adenocarcinoma is the most common type.Numerous studies have found that long noncoding RNAs(lncRNAs)are related to the occurrence and development of colon cancer.Autophagy is a key metabolic process in the human body and has a role in affecting cancer growth.In this study,our aim was to explore the correlation between lncRNAs and colon adenocarcinoma(COAD)from the perspective of autophagy.Methods A series of bioinformatics methods were used to explore the correlation between lncRNA and COAD from the perspective of autophagy.Results Four autophagy-related lncRNAs related to the prognosis of COAD were identified:EB1-AS1,LINC02381,AC011462.4,and AC016876.1.These four lncRNAs may act as oncogenes involved in the occurrence and development of COAD.The prognostic model was established,and the accuracy of the model was verified by the receiver operating characteristic curve.The risk score of the model could independently predict the prognosis of patients and was preferable to other clinical indicators,with higher values indicating a worse prognosis of the patients.Gene Set Enrichment Analysis was performed for these four lncRNAs,which showed that the high expression group of these were enriched in the basal cell carcinoma pathway.To make it more convenient for clinicians to use,we constructed a nomogram based on age and risk score,which can be used to evaluate the one-,three-,and five-year survival rates of patients.Conclusion These results can help us understand the mechanism of action of lncRNA on COAD from the perspective of autophagy and may provide new directions for the diagnosis and treatment of COAD.The EB1-AS1 gene in this study is a potential candidate biological target for COAD treatment in the future. 展开更多
关键词 colon adenocarcinoma(coad) prognostic model long noncoding RNA(lncRNA) EB1-AS1
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c-Met作为嵌合抗原受体T(CAR-T)细胞治疗结肠癌靶点的生物信息学预测及验证
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作者 彭上 闵静婷 +4 位作者 龙赤荣 谢梓龙 张露 李海鹏 李正红 《细胞与分子免疫学杂志》 CAS CSCD 北大核心 2024年第7期614-622,共9页
目的探索细胞间充质上皮转化因子(c-Met)作为嵌合抗原受体T(CAR-T)细胞治疗结肠癌有效靶点的可能性。方法通过生物信息学方法分析c-Met在结肠腺癌(COAD)中的特异性表达及其临床意义;使用免疫组织化学验证结肠癌临床患者肿瘤组织中c-Met... 目的探索细胞间充质上皮转化因子(c-Met)作为嵌合抗原受体T(CAR-T)细胞治疗结肠癌有效靶点的可能性。方法通过生物信息学方法分析c-Met在结肠腺癌(COAD)中的特异性表达及其临床意义;使用免疫组织化学验证结肠癌临床患者肿瘤组织中c-Met的表达,采用流式细胞术检测HCT116结肠癌细胞株中c-Met的表达;使用慢病毒感染人外周血单个核细胞(PBMC)中原代T细胞,制备靶向c-Met的二代CAR-T细胞,并观察c-Met CAR-T细胞对HCT116细胞的抑制效果。结果免疫组织化学与生物信息学显示c-Met在COAD中高表达,其中相对低表达的患者生存预后较好,在正常结肠组织中低表达或不表达。流式细胞术显示c-Met在HCT116细胞中也高表达。c-Met CAR-T细胞能够靶向表达抗原的肿瘤细胞,并且在抗原刺激下,CAR-T细胞特异性增殖,起到杀伤癌细胞与释放白细胞介素2(IL-2)和γ干扰素(IFN-γ)的生物学作用。结论c-Met有成为COAD潜在治疗靶点的潜能;c-Met CAR-T细胞在体外对结肠癌细胞具有抑制作用。 展开更多
关键词 嵌合抗原受体T(CAR-T)细胞 结肠腺癌(coad) 细胞间充质上皮转化因子(c-Met) 生物信息学
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