Article(id=1291704950514536995, tenantId=1146029695717560320, journalId=1246415772164075586, issueId=1291704892859638107, articleNumber=null, orderNo=null, doi=10.13699/j.cnki.1001-6821.2025.19.012, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1746460800000, receivedDateStr=2025-05-06, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1785896058919, onlineDateStr=2026-08-05, pubDate=1760630400000, pubDateStr=2025-10-17, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1785896058919, onlineIssueDateStr=2026-08-05, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1785896058919, creator=13701087609, updateTime=1785896058919, updator=13701087609, issue=Issue{id=1291704892859638107, tenantId=1146029695717560320, journalId=1246415772164075586, year='2025', volume='41', issue='19', pageStart='2701', pageEnd='2850', issueExtLink='null', onlineDate='null', pubDate='1760630400000', pubDateStr='2025-10-17', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1785896045171, creator='13701087609', updateTime=1785896787712, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1291708007352656266, tenantId=1146029695717560320, journalId=1246415772164075586, issueId=1291704892859638107, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1291708007352656267, tenantId=1146029695717560320, journalId=1246415772164075586, issueId=1291704892859638107, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=2767, endPage=2773, ext={EN=ArticleExt(id=1291704950732640804, articleId=1291704950514536995, tenantId=1146029695717560320, journalId=1246415772164075586, language=EN, title=Research of andrographolide modulates epithelial-mesenchymal transition in oral squamous cell carcinoma by miR-218-5p/SOX5 pathways, columnId=1246531407326105792, journalTitle=Chinese Journal of Clinical Pharmacology, columnName=Clinical and Basic Bridging Research, runingTitle=null, highlight=null, articleAbstract=
Objective

To investigate the effects of andrographolide on microRNA (miR) -218-5p/RY box transcription factor 5 (SOX5) on the proliferation, invasion and epithelial mesenchymal transformation (EMT) of oral squamous cell carcinoma cells.

Methods

CAL-27 cells were divided into the following groups: blank group (conventional culture), andrographolide group (treated with 15 μmol·L-1 andrographolide), andrographolide + inhibitor NC group (treated with 15 μmol·L-1 andrographolide and transfected with inhibitor NC), andrographolide + miR-218-5p inhibitor group (treated with 15 μmol·L-1 andrographolide and transfected with miR-218-5p inhibitor), andrographolide + miR-218-5p inhibitor + si-NC group (treated with 15 μmol·L-1 andrographolide and co-transfected with miR-218-5p inhibitor and si-NC), and andrographolide + miR-218-5p inhibitor + si-SOX5 group (treated with 15 μmol·L-1 andrographolide and co-transfected with miR-218-5p inhibitor and si-SOX5). The relative expression levels of miR-218-5p and SOX5 mRNA were detected by quantitative reverse transcription polymerase chain reaction (qRT-PCR), cell proliferation ability was measured using the 5-ethynyl-2′-deoxyuridine (EdU) assay, cell invasion ability was assessed by Transwell assay, and the relative expression levels of EMT-related proteins were determined by Western blotting.

Results

After different treatment periods, the relative expression levels of miR-218-5p in blank group, andrographolide group, andrographolide + inhibitor NC group and andrographolide + miR-218-5p inhibitor group were 1.00±0.11, 2.76±0.48, 2.69±0.50 and 1.19±0.17, respectively; the relative expression levels of SOX5 mRNA were 1.00±0.09, 0.36±0.07, 0.35±0.05 and 0.93±0.18, respectively. Compared with the blank group, the andrographolide group showed statistically significantly upregulated miR-218-5p relative expression levels and statistically significantly reduced SOX5 mRNA relative expression levels (all P<0.05). The proliferation rates in blank group, andrographolide group, andrographolide + inhibitor NC group, andrographolide + miR-218-5p inhibitor group, andrographolide + miR-218-5p inhibitor + si-NC group and andrographolide + miR-218-5p inhibitor + si-SOX5 group were (62.76±8.14)%, (23.58±2.87)%, (25.12±3.64)%, (51.29±9.12)%, (50.76±8.29)% and (34.18±6.83)%, respectively; the number of invasive cells were (154.23±17.24), (67.13±9.37), (72.81±11.28), (125.36±18.74), (118.15±19.80) and (80.44±12.13), respectively; the relative expression levels of E-cadherin were 1.00±0.12, 2.62±0.43, 2.56±0.47, 1.47±0.27, 1.51±0.23 and 2.24±0.43, respectively; the relative expression levels of N-cadherin were 1.00±0.11, 0.41±0.08, 0.39±0.06, 0.83±0.17, 0.86±0.15 and 0.51±0.10, respectively; the relative expression levels of Vimentin were 1.00±0.08, 0.49±0.07, 0.46±0.09, 0.85±0.16, 0.88±0.17 and 0.55±0.11, respectively. Compared with blank group, andrographolide group showed statistically significantly decreased proliferation rate, number of invasive cells and relative expression levels of N-cadherin and Vimentin, while demonstrating statistically significantly increased relative expression levels of E-cadherin (all P<0.05).

Conclusion

Andrographolide inhibits the proliferation, invasion, and EMT in oral squamous cell carcinoma, potentially through upregulating miR-218-5p and subsequently targeting the suppression of SOX5 expression.

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目的

探讨穿心莲内酯调节微小RNA(miR)-218-5p/SRY-box转录因子5(SOX5)对口腔鳞状细胞癌细胞增殖、侵袭和上皮间质转化(EMT)的影响。

方法

将CAL-27细胞分为空白组(常规培养)、穿心莲内酯组(15 μmol·L-1穿心莲内酯处理)、穿心莲内酯+inhibitor NC组(15 μmol·L-1穿心莲内酯+转染inhibitor NC处理)、穿心莲内酯+miR-218-5p inhibitor组(15 μmol·L-1穿心莲内酯+转染miR-218-5p inhibitor处理)、穿心莲内酯+miR-218-5p inhibitor+si-NC组(15 μmol·L-1穿心莲内酯+共转染miR-218-5p inhibitor和si-NC处理)和穿心莲内酯+miR-218-5p inhibitor+si-SOX5组(15 μmol·L-1穿心莲内酯+共转染miR-218-5p inhibitor和si-SOX5处理)。用定量逆转录聚合酶链反应(qRT-PCR)检测miR-218-5p与SOX5 mRNA的相对表达水平;用5-乙炔基-2′-脱氧尿苷(EdU)法检测细胞增殖能力,用Transwell法检测细胞侵袭能力,用蛋白质印迹法检测EMT相关蛋白的相对表达水平。

结果

经过不同时间处理后,空白组、穿心莲内酯组、穿心莲内酯+inhibitor NC组和穿心莲内酯+miR-218-5p inhibitor组中miR-218-5p相对表达水平分别为1.00±0.11、2.76±0.48、2.69±0.50和1.19±0.17,SOX5 mRNA的相对表达水平分别为1.00±0.09、0.36±0.07、0.35±0.05和0.93±0.18。与空白组相比,穿心莲内酯组的miR-218-5p相对表达水平显著上调,SOX5 mRNA相对表达水平显著下调(均P<0.05)。空白组、穿心莲内酯组、穿心莲内酯+inhibitor NC组、穿心莲内酯+miR-218-5p inhibitor组、穿心莲内酯+miR-218-5p inhibitor+si-NC组和穿心莲内酯+miR-218-5p inhibitor+si-SOX5组的增殖率分别为(62.76±8.14)%、(23.58±2.87)%、(25.12±3.64)%、(51.29±9.12)%、(50.76±8.29)%和(34.18±6.83)%,侵袭个数分别为(154.23±17.24)、(67.13±9.37)、(72.81±11.28)、(125.36±18.74)、(118.15±19.80)和(80.44±12.13)个,E-钙黏蛋白(E-cadherin)相对表达水平分别为1.00±0.12、2.62±0.43、2.56±0.47、1.47±0.27、1.51±0.23和2.24±0.43,神经钙黏蛋白(N-cadherin)相对表达水平分别为1.00±0.11、0.41±0.08、0.39±0.06、0.83±0.17、0.86±0.15和0.51±0.10,波形蛋白(Vimentin)相对表达水平分别为1.00±0.08、0.49±0.07、0.46±0.09、0.85±0.16、0.88±0.17和0.55±0.11。与空白组相比,穿心莲内酯组的增殖率、侵袭个数及N-cadherin与Vimentin相对表达水平均显著降低,E-cadherin相对表达水平显著升高(均P<0.05)。

结论

穿心莲内酯可抑制口腔鳞状细胞癌的增殖、侵袭和EMT,其机制可能与上调miR-218-5p从而靶向抑制SOX5的表达有关。

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张芳英(1988-),女,主管药师,主要从事临床药学、基础医学方面的工作和研究

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黄根生,副主任医师 MP: 15879748676 E-mail:
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穿心莲内酯调节miR-218-5p/SOX5影响口腔鳞状细胞癌细胞上皮间质转化的研究
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张芳英 a , 黄新帮 b , 黄迪 c , 曾以旺 a , 黄根生 c
中国临床药理学杂志 | 临床与基础桥接研究 2025,41(19): 2767-2773
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中国临床药理学杂志 |临床与基础桥接研究 2025 , 41 (19) : 2767 -2773
穿心莲内酯调节miR-218-5p/SOX5影响口腔鳞状细胞癌细胞上皮间质转化的研究
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张芳英(1988-),女,主管药师,主要从事临床药学、基础医学方面的工作和研究

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张芳英a, 黄新帮b, 黄迪c, 曾以旺a, 黄根生c
作者信息
  • a.赣州市人民医院,药剂科,江西 赣州 341000
  • b.赣州市人民医院,口腔颌面外科,江西 赣州 341000
  • c.赣州市人民医院,口腔科,江西 赣州 341000
通讯作者:
黄根生,副主任医师 MP: 15879748676 E-mail:
作者简介:

张芳英(1988-),女,主管药师,主要从事临床药学、基础医学方面的工作和研究

Research of andrographolide modulates epithelial-mesenchymal transition in oral squamous cell carcinoma by miR-218-5p/SOX5 pathways
Fang-ying ZHANGa, Xin-bang HUANGb, Di HUANGc, Yi-wang ZENGa, Gen-sheng HUANGc
Affiliations
  • a.Department of Pharmacy, Ganzhou People’s Hospital, Ganzhou 341000, Jiangxi Province, China
  • b.Department of Maxillofacial Surgery, Ganzhou People’s Hospital, Ganzhou 341000, Jiangxi Province, China
  • c.Department of Stomatology, Ganzhou People’s Hospital, Ganzhou 341000, Jiangxi Province, China
出版时间: 2025-10-17 doi: 10.13699/j.cnki.1001-6821.2025.19.012
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目的

探讨穿心莲内酯调节微小RNA(miR)-218-5p/SRY-box转录因子5(SOX5)对口腔鳞状细胞癌细胞增殖、侵袭和上皮间质转化(EMT)的影响。

方法

将CAL-27细胞分为空白组(常规培养)、穿心莲内酯组(15 μmol·L-1穿心莲内酯处理)、穿心莲内酯+inhibitor NC组(15 μmol·L-1穿心莲内酯+转染inhibitor NC处理)、穿心莲内酯+miR-218-5p inhibitor组(15 μmol·L-1穿心莲内酯+转染miR-218-5p inhibitor处理)、穿心莲内酯+miR-218-5p inhibitor+si-NC组(15 μmol·L-1穿心莲内酯+共转染miR-218-5p inhibitor和si-NC处理)和穿心莲内酯+miR-218-5p inhibitor+si-SOX5组(15 μmol·L-1穿心莲内酯+共转染miR-218-5p inhibitor和si-SOX5处理)。用定量逆转录聚合酶链反应(qRT-PCR)检测miR-218-5p与SOX5 mRNA的相对表达水平;用5-乙炔基-2′-脱氧尿苷(EdU)法检测细胞增殖能力,用Transwell法检测细胞侵袭能力,用蛋白质印迹法检测EMT相关蛋白的相对表达水平。

结果

经过不同时间处理后,空白组、穿心莲内酯组、穿心莲内酯+inhibitor NC组和穿心莲内酯+miR-218-5p inhibitor组中miR-218-5p相对表达水平分别为1.00±0.11、2.76±0.48、2.69±0.50和1.19±0.17,SOX5 mRNA的相对表达水平分别为1.00±0.09、0.36±0.07、0.35±0.05和0.93±0.18。与空白组相比,穿心莲内酯组的miR-218-5p相对表达水平显著上调,SOX5 mRNA相对表达水平显著下调(均P<0.05)。空白组、穿心莲内酯组、穿心莲内酯+inhibitor NC组、穿心莲内酯+miR-218-5p inhibitor组、穿心莲内酯+miR-218-5p inhibitor+si-NC组和穿心莲内酯+miR-218-5p inhibitor+si-SOX5组的增殖率分别为(62.76±8.14)%、(23.58±2.87)%、(25.12±3.64)%、(51.29±9.12)%、(50.76±8.29)%和(34.18±6.83)%,侵袭个数分别为(154.23±17.24)、(67.13±9.37)、(72.81±11.28)、(125.36±18.74)、(118.15±19.80)和(80.44±12.13)个,E-钙黏蛋白(E-cadherin)相对表达水平分别为1.00±0.12、2.62±0.43、2.56±0.47、1.47±0.27、1.51±0.23和2.24±0.43,神经钙黏蛋白(N-cadherin)相对表达水平分别为1.00±0.11、0.41±0.08、0.39±0.06、0.83±0.17、0.86±0.15和0.51±0.10,波形蛋白(Vimentin)相对表达水平分别为1.00±0.08、0.49±0.07、0.46±0.09、0.85±0.16、0.88±0.17和0.55±0.11。与空白组相比,穿心莲内酯组的增殖率、侵袭个数及N-cadherin与Vimentin相对表达水平均显著降低,E-cadherin相对表达水平显著升高(均P<0.05)。

结论

穿心莲内酯可抑制口腔鳞状细胞癌的增殖、侵袭和EMT,其机制可能与上调miR-218-5p从而靶向抑制SOX5的表达有关。

穿心莲内酯  /  口腔鳞状细胞癌  /  增殖  /  侵袭  /  上皮间质转化
Objective

To investigate the effects of andrographolide on microRNA (miR) -218-5p/RY box transcription factor 5 (SOX5) on the proliferation, invasion and epithelial mesenchymal transformation (EMT) of oral squamous cell carcinoma cells.

Methods

CAL-27 cells were divided into the following groups: blank group (conventional culture), andrographolide group (treated with 15 μmol·L-1 andrographolide), andrographolide + inhibitor NC group (treated with 15 μmol·L-1 andrographolide and transfected with inhibitor NC), andrographolide + miR-218-5p inhibitor group (treated with 15 μmol·L-1 andrographolide and transfected with miR-218-5p inhibitor), andrographolide + miR-218-5p inhibitor + si-NC group (treated with 15 μmol·L-1 andrographolide and co-transfected with miR-218-5p inhibitor and si-NC), and andrographolide + miR-218-5p inhibitor + si-SOX5 group (treated with 15 μmol·L-1 andrographolide and co-transfected with miR-218-5p inhibitor and si-SOX5). The relative expression levels of miR-218-5p and SOX5 mRNA were detected by quantitative reverse transcription polymerase chain reaction (qRT-PCR), cell proliferation ability was measured using the 5-ethynyl-2′-deoxyuridine (EdU) assay, cell invasion ability was assessed by Transwell assay, and the relative expression levels of EMT-related proteins were determined by Western blotting.

Results

After different treatment periods, the relative expression levels of miR-218-5p in blank group, andrographolide group, andrographolide + inhibitor NC group and andrographolide + miR-218-5p inhibitor group were 1.00±0.11, 2.76±0.48, 2.69±0.50 and 1.19±0.17, respectively; the relative expression levels of SOX5 mRNA were 1.00±0.09, 0.36±0.07, 0.35±0.05 and 0.93±0.18, respectively. Compared with the blank group, the andrographolide group showed statistically significantly upregulated miR-218-5p relative expression levels and statistically significantly reduced SOX5 mRNA relative expression levels (all P<0.05). The proliferation rates in blank group, andrographolide group, andrographolide + inhibitor NC group, andrographolide + miR-218-5p inhibitor group, andrographolide + miR-218-5p inhibitor + si-NC group and andrographolide + miR-218-5p inhibitor + si-SOX5 group were (62.76±8.14)%, (23.58±2.87)%, (25.12±3.64)%, (51.29±9.12)%, (50.76±8.29)% and (34.18±6.83)%, respectively; the number of invasive cells were (154.23±17.24), (67.13±9.37), (72.81±11.28), (125.36±18.74), (118.15±19.80) and (80.44±12.13), respectively; the relative expression levels of E-cadherin were 1.00±0.12, 2.62±0.43, 2.56±0.47, 1.47±0.27, 1.51±0.23 and 2.24±0.43, respectively; the relative expression levels of N-cadherin were 1.00±0.11, 0.41±0.08, 0.39±0.06, 0.83±0.17, 0.86±0.15 and 0.51±0.10, respectively; the relative expression levels of Vimentin were 1.00±0.08, 0.49±0.07, 0.46±0.09, 0.85±0.16, 0.88±0.17 and 0.55±0.11, respectively. Compared with blank group, andrographolide group showed statistically significantly decreased proliferation rate, number of invasive cells and relative expression levels of N-cadherin and Vimentin, while demonstrating statistically significantly increased relative expression levels of E-cadherin (all P<0.05).

Conclusion

Andrographolide inhibits the proliferation, invasion, and EMT in oral squamous cell carcinoma, potentially through upregulating miR-218-5p and subsequently targeting the suppression of SOX5 expression.

andrographolide  /  oral squamous cell carcinoma  /  proliferation  /  invade and attack  /  epithelial mesenchymal transformation
张芳英, 黄新帮, 黄迪, 曾以旺, 黄根生. 穿心莲内酯调节miR-218-5p/SOX5影响口腔鳞状细胞癌细胞上皮间质转化的研究. 中国临床药理学杂志, 2025 , 41 (19) : 2767 -2773 . DOI: 10.13699/j.cnki.1001-6821.2025.19.012
Fang-ying ZHANG, Xin-bang HUANG, Di HUANG, Yi-wang ZENG, Gen-sheng HUANG. Research of andrographolide modulates epithelial-mesenchymal transition in oral squamous cell carcinoma by miR-218-5p/SOX5 pathways[J]. Chinese Journal of Clinical Pharmacology, 2025 , 41 (19) : 2767 -2773 . DOI: 10.13699/j.cnki.1001-6821.2025.19.012
  • 江西省卫生健康委科技计划基金资助项目(SKJP220236690)
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doi: 10.13699/j.cnki.1001-6821.2025.19.012
  • 接收时间:2025-05-06
  • 首发时间:2026-08-05
  • 出版时间:2025-10-17
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  • 收稿日期:2025-05-06
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江西省卫生健康委科技计划基金资助项目(SKJP220236690)
作者信息
    a.赣州市人民医院,药剂科,江西 赣州 341000
    b.赣州市人民医院,口腔颌面外科,江西 赣州 341000
    c.赣州市人民医院,口腔科,江西 赣州 341000

通讯作者:

黄根生,副主任医师 MP: 15879748676 E-mail:
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鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
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红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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