Downregulation of SOX21-AS1 Alleviated Cisplatin Resistance in Cervical Cancer Through Epithelial-Mesenchymal Transition Inhibition.

IF 2.2 4区 医学 Q3 GERIATRICS & GERONTOLOGY
Rejuvenation research Pub Date : 2022-10-01 Epub Date: 2022-10-12 DOI:10.1089/rej.2022.0009
Jing Tian, Ze Li, Yuanyuan Jiang, Wenjin Gu, Enqi Kong, Quan Hao, Beihua Kong, Li Sun
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引用次数: 3

Abstract

Cisplatin is widely used in chemotherapies in cervical cancer (CC). Nevertheless, drug resistance in cancer patients poses a major threat to efficacy of treatment. To explore the underlying modulatory mechanism of SOX21-AS1 in cisplatin resistance in CC cell and mice models, Gepia database was referred for SOX21-AS1 expression in cancer tissues and normal ones. Reverse transcription quantitative real-time polymerase chain reaction was used to measure the differential expression of SOX21-AS1 in parental Siha cells and cisplatin-resistant Siha/DDP cells. Luciferase reporter gene assays were conducted to verify putative bindings between SOX21-AS1 and miR-9-3p. Western blot method was employed to evaluate the changes in cleaved-caspase 7 protein expression. Cisplatin resistance was evaluated in each transfected group using cell counting kit 8 method after cells were exposed to cisplatin (0, 7.5, 15, 30, 60, 120, and 240 μg/mL) for 24 hours. Flow cytometry method was used to measure the apoptosis rates. Cell migration and invasion were measured using Transwell assays. Immunofluorescence method was applied to observe epithelial to mesenchymal transition (EMT) markers, including E-cadherin, Snail, matrix metalloproteinase (MMP)3, and MMP9. Siha/DDP cell groups stably transfected with sh-NC and sh-SOX21-AS1 were injected through tail vein of Balb/C mice. Lung tissue sections were used for hematoxylin and eosin staining and immunohistochemistry analysis. SOX1-AS1 expression was higher in cancer tissues than normal ones and was also higher in Siha/DDP rather than Siha cells. SOX21-AS1 was targeted by miR-9-3p in CC cells. Downregulation of SOX21-AS1 or overexpression of miR-9-3p inhibited cisplatin resistance in Siha/DDP cells and reduced cell invasion and migration and attenuated EMT progression. In vivo, the SOX21-AS1 knockdown led to less severe lung metastasis. Downregulation of SOX21-AS1 alleviated cisplatin resistance in CC through EMT inhibition.

SOX21-AS1下调通过上皮-间质转化抑制减轻宫颈癌顺铂耐药
顺铂广泛应用于宫颈癌的化疗。然而,癌症患者的耐药性对治疗效果构成了重大威胁。为了探讨SOX21-AS1在CC细胞和小鼠模型顺铂耐药中的潜在调节机制,我们参考Gepia数据库,查询SOX21-AS1在癌组织和正常组织中的表达情况。采用逆转录定量实时聚合酶链反应测定SOX21-AS1在亲代Siha细胞和顺铂耐药Siha/DDP细胞中的差异表达。荧光素酶报告基因检测验证了SOX21-AS1与miR-9-3p之间的推测结合。Western blot法检测caspase - 7蛋白表达变化。各组细胞暴露于顺铂(0、7.5、15、30、60、120、240 μg/mL) 24h后,采用细胞计数试剂盒8法评估各组细胞对顺铂的耐药性。流式细胞术检测细胞凋亡率。采用Transwell法测定细胞迁移和侵袭。采用免疫荧光法观察上皮向间充质转化(EMT)标志物,包括E-cadherin、Snail、基质金属蛋白酶(MMP)3和MMP9。通过Balb/C小鼠尾静脉注射稳定转染sh-NC和sh-SOX21-AS1的Siha/DDP细胞组。肺组织切片进行苏木精、伊红染色及免疫组化分析。SOX1-AS1在癌组织中的表达高于正常组织,在Siha/DDP中的表达高于Siha细胞。SOX21-AS1在CC细胞中被miR-9-3p靶向。下调SOX21-AS1或过表达miR-9-3p可抑制Siha/DDP细胞的顺铂耐药,减少细胞侵袭和迁移,减缓EMT进展。在体内,SOX21-AS1敲低导致较不严重的肺转移。SOX21-AS1下调可通过EMT抑制减轻CC患者的顺铂耐药。
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来源期刊
Rejuvenation research
Rejuvenation research 医学-老年医学
CiteScore
4.50
自引率
0.00%
发文量
41
审稿时长
3 months
期刊介绍: Rejuvenation Research publishes cutting-edge, peer-reviewed research on rejuvenation therapies in the laboratory and the clinic. The Journal focuses on key explorations and advances that may ultimately contribute to slowing or reversing the aging process, and covers topics such as cardiovascular aging, DNA damage and repair, cloning, and cell immortalization and senescence. Rejuvenation Research coverage includes: Cell immortalization and senescence Pluripotent stem cells DNA damage/repair Gene targeting, gene therapy, and genomics Growth factors and nutrient supply/sensing Immunosenescence Comparative biology of aging Tissue engineering Late-life pathologies (cardiovascular, neurodegenerative and others) Public policy and social context.
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