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CD44s在头颈部癌细胞中诱导miR-629-3p表达并与顺铂耐药相关。

CD44s Induces miR-629-3p Expression in Association with Cisplatin Resistance in Head and Neck Cancer Cells.

作者信息

Chikuda Junichiro, Otsuka Kurataka, Shimomura Iwao, Ito Kagenori, Miyazaki Hiroaki, Takahashi Ryou-U, Nagasaki Masahiro, Mukudai Yoshiki, Ochiya Takahiro, Shimane Toshikazu, Shirota Tatsuo, Yamamoto Yusuke

机构信息

Division of Cellular Signaling, National Cancer Center Research Institute, Tokyo 104-0045, Japan.

Department of Oral and Maxillofacial Surgery, Showa University School of Dentistry, Tokyo 145-8515, Japan.

出版信息

Cancers (Basel). 2020 Apr 1;12(4):856. doi: 10.3390/cancers12040856.

Abstract

Cisplatin (cis-diamminedichloroplatinum II [CDDP] ) is a well-known chemotherapeutic drug that has been used for the treatment of various types of human cancers, including head and neck cancer. Cisplatin exerts anticancer effects by causing DNA damage, replication defects, transcriptional inhibition, cell cycle arrest, and the induction of apoptosis. However, drug resistance is one of the most serious problems with cancer chemotherapy, and it causes expected therapeutic effects to not always be achieved. Here, we analyzed global microRNA (miRNA) expression in CD44 standard form (CD44s)-expressing SAS cells, and we identified miR-629-3p as being responsible for acquiring anticancer drug resistance in head and neck cancer. The introduction of miR-629-3p expression inhibited apoptotic cell death under cisplatin treatment conditions, and it promoted cell migration. Among the computationally predicted target genes of miR-629-3p, we found that a number of gene expressions were suppressed by the transfection with miR-629-3p. Using a xenografting model, we showed that miR-629-3p conferred cisplatin resistance to SAS cells. Clinically, increased miR-629-3p expression tended to be associated with decreased survival in head and neck cancer patients. In conclusion, our data suggest that the increased expression of miR-629-3p provides a mechanism of cisplatin resistance in head and neck cancer and may serve as a therapeutic target to reverse chemotherapy resistance.

摘要

顺铂(顺二氨二氯铂II [CDDP])是一种著名的化疗药物,已被用于治疗包括头颈癌在内的各种类型的人类癌症。顺铂通过引起DNA损伤、复制缺陷、转录抑制、细胞周期停滞和诱导细胞凋亡来发挥抗癌作用。然而,耐药性是癌症化疗中最严重的问题之一,它导致预期的治疗效果无法总是实现。在这里,我们分析了表达CD44标准形式(CD44s)的SAS细胞中的全局微小RNA(miRNA)表达,并确定miR-629-3p是头颈癌获得抗癌药物耐药性的原因。miR-629-3p表达的引入在顺铂治疗条件下抑制了凋亡细胞死亡,并促进了细胞迁移。在miR-629-3p的计算预测靶基因中,我们发现许多基因表达通过转染miR-629-3p而受到抑制。使用异种移植模型,我们表明miR-629-3p赋予了SAS细胞顺铂耐药性。临床上,miR-629-3p表达的增加往往与头颈癌患者生存率的降低有关。总之,我们的数据表明,miR-629-3p表达的增加提供了头颈癌顺铂耐药的机制,并可能作为逆转化疗耐药性的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b3/7226407/26bb9730ac8e/cancers-12-00856-g001.jpg

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