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放疗和化疗引起的黏膜炎潜在分子机制及候选药物的鉴定

Identification of potential molecular mechanisms and candidate drugs for radiotherapy- and chemotherapy-induced mucositis.

作者信息

Hao Siyuan, Jin Yixin, Yu Yue, Wang Jiantao, Zou Jing, Wang Yan

机构信息

State Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases & Department of Pediatric Dentistry, West China Hospital of Stomatology, Sichuan University, No. 14, 3rd Section, S. Renmin Road, Chengdu, 610041, People's Republic of China.

State Key Laboratory of Biotherapy and Department of Lung Cancer Center and Department of Radiation Oncology, West China Hospital, Sichuan University, Chengdu, China.

出版信息

Support Care Cancer. 2023 Mar 20;31(4):223. doi: 10.1007/s00520-023-07686-7.

Abstract

BACKGROUND

Radiotherapy-induced oral mucositis (RIOM) and chemotherapy-induced oral mucositis (CIOM) are common complications in cancer patients, leading to negative clinical manifestations, reduced quality of life, and unsatisfactory treatment outcomes.

OBJECTIVE

The present study aimed to identify potential molecular mechanisms and candidate drugs by data mining.

METHODS

We obtained a preliminary list of genes associated with RIOM and CIOM. In-depth information on these genes was explored by functional and enrichment analyses. Then, the drug-gene interaction database was used to determine the interaction of the final enriched gene list with known drugs and analyze the drug candidates.

RESULTS AND CONCLUSION

This study identified 21 hub genes that may play an important role in RIOM and CIOM, respectively. Through our data mining, bioinformatics survey, and candidate drug selection, TNF, IL-6, and TLR9 could play an important role in disease progression and treatment. In addition, eight candidate drugs (olokizumab, chloroquine, hydroxychloroquine, adalimumab, etanercept, golimumab, infliximab, and thalidomide) were selected by the drug-gene interaction literature search additionally, as candidates for treating RIOM and CIOM.

摘要

背景

放疗诱导的口腔黏膜炎(RIOM)和化疗诱导的口腔黏膜炎(CIOM)是癌症患者常见的并发症,会导致负面的临床表现、生活质量下降以及治疗效果不理想。

目的

本研究旨在通过数据挖掘确定潜在的分子机制和候选药物。

方法

我们获得了与RIOM和CIOM相关的基因初步列表。通过功能和富集分析探索这些基因的深入信息。然后,利用药物-基因相互作用数据库确定最终富集基因列表与已知药物的相互作用并分析候选药物。

结果与结论

本研究分别鉴定出21个可能在RIOM和CIOM中起重要作用的枢纽基因。通过我们的数据挖掘、生物信息学调查和候选药物选择,肿瘤坏死因子(TNF)、白细胞介素-6(IL-6)和Toll样受体9(TLR9)可能在疾病进展和治疗中起重要作用。此外,通过药物-基因相互作用文献检索额外选择了8种候选药物(奥洛珠单抗、氯喹、羟氯喹、阿达木单抗、依那西普、戈利木单抗、英夫利昔单抗和沙利度胺)作为治疗RIOM和CIOM的候选药物。

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