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利用唾液中的miR-375作为口腔潜在恶性疾病的临床生物标志物。

Exploiting salivary miR-375 as a clinical biomarker of oral potentially malignant disorder.

作者信息

Tu Hsi-Feng, Lin Li-Han, Chang Kuo-Wei, Cheng Hui-Wen, Liu Chung-Ji

机构信息

Department of Dentistry, National Yang Ming Chiao Tung Hospital, Yi-Lan, Taiwan.

Department of Dentistry, College of Dentistry, National Yang Ming Chiao Tung University, Taipei, Taiwan.

出版信息

J Dent Sci. 2022 Apr;17(2):659-665. doi: 10.1016/j.jds.2021.09.020. Epub 2021 Sep 20.

Abstract

BACKGROUND/PURPOSE: Oral potentially malignant disorder (OPMD) is an important premalignancy worldwide. MicroRNAs (miRNAs) are endogenously expressed non-coding RNAs that regulate the post-transcriptional levels of targeted mRNAs. () is markedly downregulated in oral carcinoma tissues and plays an oncogenic role in oral carcinogenesis. We explored the potential of the deregulated salivary levels in OPMD patients.

MATERIALS AND METHODS

We analyzed the levels of in the saliva of patients with OPMD ( = 45) and healthy controls ( = 24) by quantitative RT-PCR. The cell lysates and supernatants were treated with the miR-375 mimic and inhibitor.

RESULTS

Salivary levels were decreased markedly in the patients with OPMD, compared with the controls. OPMD patients with non-dysplasia showed a higher abundance of in the saliva than dysplasia patients, suggesting that salivary is a more sensitive marker for OPMD. Patients with malignant transformation during the follow-up period showed lower expression of saliva than the others. expression was markedly decreased by treatment with the miR-375 inhibitor, and the supernatants of both NHOK and SAS cells showed a corresponding decline in expression.

CONCLUSION

Our results indicate the potential application of salivary as a biomarker for the detection and long-term follow-up of OPMD.

摘要

背景/目的:口腔潜在恶性疾病(OPMD)是全球范围内一种重要的癌前病变。微小RNA(miRNA)是内源性表达的非编码RNA,可调节靶标mRNA的转录后水平。()在口腔癌组织中显著下调,并在口腔癌发生过程中发挥致癌作用。我们探讨了OPMD患者唾液中该指标失调的可能性。

材料与方法

我们通过定量逆转录聚合酶链反应分析了45例OPMD患者和24例健康对照者唾液中的水平。细胞裂解物和上清液分别用miR-375模拟物和抑制剂处理。

结果

与对照组相比,OPMD患者唾液中的水平显著降低。非发育异常的OPMD患者唾液中的丰度高于发育异常患者,这表明唾液是OPMD更敏感的标志物。随访期间发生恶性转化的患者唾液中的表达低于其他患者。用miR-375抑制剂处理后,表达明显降低,NHOK和SAS细胞的上清液中的表达也相应下降。

结论

我们的结果表明唾液作为OPMD检测和长期随访生物标志物的潜在应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52d7/9201538/d7186f522096/gr1.jpg

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