Article(id=1322926479255937406, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322926217711726961, articleNumber=null, orderNo=null, doi=10.13193/j.issn.1673-7717.2025.08.019, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=null, receivedDateStr=null, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1793339851440, onlineDateStr=2026-10-30, pubDate=1754755200000, pubDateStr=2025-08-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793339851440, onlineIssueDateStr=2026-10-30, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793339851440, creator=13701087609, updateTime=1793339851440, updator=13701087609, issue=Issue{id=1322926217711726961, tenantId=1146029695717560320, journalId=1255847919539208197, year='2025', volume='43', issue='8', pageStart='1', pageEnd='258', issueExtLink='null', onlineDate='null', pubDate='1754755200000', pubDateStr='2025-08-10', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=0, createTime=1793339789083, creator='13701087609', updateTime=1793340517761, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1322929274071679978, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322926217711726961, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1322929274071679979, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322926217711726961, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=88, endPage=91, ext={EN=ArticleExt(id=1322926479495012735, articleId=1322926479255937406, tenantId=1146029695717560320, journalId=1255847919539208197, language=EN, title=Effect of Shikonin on Cell Proliferation,Migration,Invasion and Apoptosis of NPC Cells by Regulating miR-224 Expression, columnId=1256183361521967297, journalTitle=Chinese Archives of Traditional Chinese Medicine, columnName=Target on National Project, runingTitle=null, highlight=null, articleAbstract=
Objective

To investigate the effect of shikonin on the cell proliferation,migration,invasion and apoptosis of nasopharyngeal carcinoma(NPC)cells by regulating miR-224 expression.

Methods

Thirty NPC patients treated in the hospital from January 2023 to March 2024 were selected and underwent surgery.The adjacent and cancerous tissues were removed during the surgery.The normal cultured human SUNE-1 cells were recorded as the blank control group,those treated with shikonin were designated as the shikonin group.Those treated with shikonin and transfected with miR-NC and miR-224 mimetics were designated as the miR-NC and miR-224 groups.The expression of miR-224 in each group was compared,and the effects of shikonin on cell proliferation,migration,invasion and apoptosis were observed by regulating miR-224 expression.

Result

The expression of miR-224 in NPC tissue was(3.23±0.16),which was higher than that(1.09±0.07)in adjacent tissues(P<0.05). Comparison of miR-224 expression among the groups:shikonin+miR-224 group>blank control group>shikonin+miR-NC group>shikonin group,and the pairwise comparisons among groups were statistically significant(P<0.05). Comparison of optical density(OD)value,number of migrating cells and number of invading cells among the groups:blank control group>miR-224 group>miR-NC group>shikonin group. Comparison of apoptosis rate among the groups:blank control group<miR-224 group<miR-NC group<shikonin group.There were statistically significant pairwise comparisons among groups(P<0.05). Comparison of CyclinD1 protein,matrix metalloproteinase2(MMP-2)protein,MMP-9 protein and B-cell lymphoma-2(Bcl-2)protein among the groups:blank control group>miR-224 group>miR-NC group>shikonin group. Comparison of cyclin-dependent kinase inhibitor 1A(p21)protein and Bcl-2 associated X protein(Bax)protein among the groups:blank control group<miR-224 group<miR-NC group<shikonin group.There were statistically significant pairwise comparisons among groups(P<0.05).

Conclusion

Shikonin can reduce the expression of miR-224 in NPC patients,inhibit the cell proliferation,migration and invasion,and induce apoptosis.

, authors=Qunzhen LI1, Jun LI1, Pei WANG2, Ting RONG1, Yana GAO1, Rong ZHANG1, Zhongyi MIAO1, authorsList=Qunzhen LI, Jun LI, Pei WANG, Ting RONG, Yana GAO, Rong ZHANG, Zhongyi MIAO, authorCompany=null, correspAuthors=Jun LI, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1322926480820412808, articleId=1322926479255937406, tenantId=1146029695717560320, journalId=1255847919539208197, language=CN, title=紫草素通过调控miR-224表达对鼻咽癌细胞增殖、迁移、侵袭及凋亡的影响研究, columnId=1256183362172142382, journalTitle=中华中医药学刊, columnName=国家项目点击, runingTitle=null, highlight=null, articleAbstract=
目的

研究紫草素通过调控miR-224表达对鼻咽癌细胞增殖、迁移、侵袭及凋亡的影响。

方法

选取2023年1月—2024年3月在医院诊治的鼻咽癌患者30例,均开展手术,在术中切除癌旁组织和癌组织,将正常培养的人鼻咽癌SUNE-1细胞记为空白对照组,将加入紫草素的记为紫草素组,将加入紫草素给予miR-NC、miR-224 mimics转染的记为miR-NC组、miR-224组,比较各组miR-224表达,紫草素通过调控miR-224表达,对细胞的增殖、迁移、侵袭和凋亡的影响。

结果

鼻咽癌组织中miR-224表达为(3.23±0.16),和癌旁组织的(1.09±0.07)相比更高(P<0.05)。miR-224表达比较:miR-224组>空白对照组>miR-NC组>紫草素组,组间两两比均有统计学意义(P<0.05)。细胞吸光度(optical density,OD)值、迁移细胞数、侵袭细胞数比较:空白对照组>miR-224组>miR-NC组>紫草素组,凋亡率比较:空白对照组<miR-224组<miR-NC组<紫草素组,组间两两比均有统计学意义(P<0.05)。细胞周期蛋白1(CyclinD1)蛋白、基质金属蛋白酶2(matrix metalloproteinase2,MMP-2)蛋白、MMP-9蛋白、B淋巴细胞瘤-2(B-cell lymphoma-2,Bcl-2)蛋白比较:空白对照组>miR-224组>miR-NC组>紫草素组,细胞周期依赖性蛋白激酶抑制因子1A(cyclin-dependent kinase inhibitor 1A,P21)蛋白、Bcl-2相关蛋白(Bcl-2 associated X protein,Bax)蛋白比较:空白对照组<miR-224组<miR-NC组<紫草素组,组间两两比均有统计学意义(P<0.05)。

结论

紫草素可降低鼻咽癌患者miR-224表达,对细胞的增殖、迁移、侵袭起到抑制作用,并对其凋亡起到诱导作用。

, authors=李群真1, 李军1, 王培2, 荣婷1, 高亚娜1, 张蓉1, 苗忠义1, authorsList=李群真, 李军, 王培, 荣婷, 高亚娜, 张蓉, 苗忠义, authorCompany=null, correspAuthors=李军, authorNote=

李群真(1981-),女,河北枣强人,主治医师,硕士,研究方向:变应性鼻炎、鼻窦炎的中西医结合治疗。

, correspAuthorsNote=
李军(1976-),男,副主任医师,硕士,研究方向:鼻科疾病的中西医结合治疗。E-mail:。
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李群真(1981-),女,河北枣强人,主治医师,硕士,研究方向:变应性鼻炎、鼻窦炎的中西医结合治疗。

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李群真(1981-),女,河北枣强人,主治医师,硕士,研究方向:变应性鼻炎、鼻窦炎的中西医结合治疗。

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组别nOD值(450 nm)迁移细胞数/(个)侵袭细胞数/(个)凋亡率/(个)
miR-224组301.43±0.09abc105.48±4.55abc92.41±4.00abc8.97±0.68abc
miR-NC组300.51±0.03ab48.63±2.35ab39.55±2.38ab27.31±1.84ab
紫草素组300.46±0.03a46.36±2.54a37.33±1.99a29.48±2.59a
空白对照组301.62±0.13119.40±5.4596.96±4.103.60±0.76
t值1 626.8082 768.2982 994.2371 817.088
P值<0.001<0.001<0.001<0.001
), ArticleFig(id=1322926486101041603, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926479255937406, language=CN, label=表1, caption=

各组鼻咽癌细胞生物学行为()

, figureFileSmall=null, figureFileBig=null, tableContent=
组别nOD值(450 nm)迁移细胞数/(个)侵袭细胞数/(个)凋亡率/(个)
miR-224组301.43±0.09abc105.48±4.55abc92.41±4.00abc8.97±0.68abc
miR-NC组300.51±0.03ab48.63±2.35ab39.55±2.38ab27.31±1.84ab
紫草素组300.46±0.03a46.36±2.54a37.33±1.99a29.48±2.59a
空白对照组301.62±0.13119.40±5.4596.96±4.103.60±0.76
t值1 626.8082 768.2982 994.2371 817.088
P值<0.001<0.001<0.001<0.001
), ArticleFig(id=1322926487766180292, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926479255937406, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
组别nCyclinD1蛋白p21蛋白MMP-2蛋白MMP-9蛋白Bcl-2蛋白Bax蛋白
miR-224组300.72±0.07abc0.41±0.07abc0.80±0.06abc0.62±0.06abc0.67±0.05abc0.34±0.04abc
miR-NC组300.32±0.05ab0.73±0.03ab0.29±0.04ab0.28±0.02ab0.23±0.03ab0.74±0.03ab
紫草素组300.27±0.04a0.77±0.03a0.26±0.02a0.24±0.04a0.19±0.03a0.78±0.05a
空白对照组300.79±0.070.28±0.030.86±0.050.71±0.050.73±0.060.25±0.03
t值616.966923.7091 526.374831.4731 240.2291 450.492
P值<0.001<0.001<0.001<0.001<0.001<0.001
), ArticleFig(id=1322926487862649285, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926479255937406, language=CN, label=表2, caption=

各组鼻咽癌细胞生物学相关蛋白比较()

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组别nCyclinD1蛋白p21蛋白MMP-2蛋白MMP-9蛋白Bcl-2蛋白Bax蛋白
miR-224组300.72±0.07abc0.41±0.07abc0.80±0.06abc0.62±0.06abc0.67±0.05abc0.34±0.04abc
miR-NC组300.32±0.05ab0.73±0.03ab0.29±0.04ab0.28±0.02ab0.23±0.03ab0.74±0.03ab
紫草素组300.27±0.04a0.77±0.03a0.26±0.02a0.24±0.04a0.19±0.03a0.78±0.05a
空白对照组300.79±0.070.28±0.030.86±0.050.71±0.050.73±0.060.25±0.03
t值616.966923.7091 526.374831.4731 240.2291 450.492
P值<0.001<0.001<0.001<0.001<0.001<0.001
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紫草素通过调控miR-224表达对鼻咽癌细胞增殖、迁移、侵袭及凋亡的影响研究
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李群真 1 , 李军 1 , 王培 2 , 荣婷 1 , 高亚娜 1 , 张蓉 1 , 苗忠义 1
中华中医药学刊 | 国家项目点击 2025,43(8): 88-91
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中华中医药学刊 |国家项目点击 2025 , 43 (8) : 88 -91
紫草素通过调控miR-224表达对鼻咽癌细胞增殖、迁移、侵袭及凋亡的影响研究
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李群真(1981-),女,河北枣强人,主治医师,硕士,研究方向:变应性鼻炎、鼻窦炎的中西医结合治疗。

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李群真(1981-),女,河北枣强人,主治医师,硕士,研究方向:变应性鼻炎、鼻窦炎的中西医结合治疗。

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李群真1, 李军1 , 王培2, 荣婷1, 高亚娜1, 张蓉1, 苗忠义1
作者信息
  • 1.河北省中医院,河北 石家庄 050011
  • 2.石家庄市中医院,河北 石家庄 050000
通讯作者:
李军(1976-),男,副主任医师,硕士,研究方向:鼻科疾病的中西医结合治疗。E-mail:。
作者简介:

李群真(1981-),女,河北枣强人,主治医师,硕士,研究方向:变应性鼻炎、鼻窦炎的中西医结合治疗。

Effect of Shikonin on Cell Proliferation,Migration,Invasion and Apoptosis of NPC Cells by Regulating miR-224 Expression
Qunzhen LI1, Jun LI1 , Pei WANG2, Ting RONG1, Yana GAO1, Rong ZHANG1, Zhongyi MIAO1
Affiliations
  • 1.Hebei Hospital of Traditional Chinese Medicine,Shijiazhuang 050011,Hebei,China
  • 2.Shijiazhuang Hospital of Traditional Chinese Medicine,Shijiazhuang 050000,Hebei,China
出版时间: 2025-08-10 doi: 10.13193/j.issn.1673-7717.2025.08.019
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目的

研究紫草素通过调控miR-224表达对鼻咽癌细胞增殖、迁移、侵袭及凋亡的影响。

方法

选取2023年1月—2024年3月在医院诊治的鼻咽癌患者30例,均开展手术,在术中切除癌旁组织和癌组织,将正常培养的人鼻咽癌SUNE-1细胞记为空白对照组,将加入紫草素的记为紫草素组,将加入紫草素给予miR-NC、miR-224 mimics转染的记为miR-NC组、miR-224组,比较各组miR-224表达,紫草素通过调控miR-224表达,对细胞的增殖、迁移、侵袭和凋亡的影响。

结果

鼻咽癌组织中miR-224表达为(3.23±0.16),和癌旁组织的(1.09±0.07)相比更高(P<0.05)。miR-224表达比较:miR-224组>空白对照组>miR-NC组>紫草素组,组间两两比均有统计学意义(P<0.05)。细胞吸光度(optical density,OD)值、迁移细胞数、侵袭细胞数比较:空白对照组>miR-224组>miR-NC组>紫草素组,凋亡率比较:空白对照组<miR-224组<miR-NC组<紫草素组,组间两两比均有统计学意义(P<0.05)。细胞周期蛋白1(CyclinD1)蛋白、基质金属蛋白酶2(matrix metalloproteinase2,MMP-2)蛋白、MMP-9蛋白、B淋巴细胞瘤-2(B-cell lymphoma-2,Bcl-2)蛋白比较:空白对照组>miR-224组>miR-NC组>紫草素组,细胞周期依赖性蛋白激酶抑制因子1A(cyclin-dependent kinase inhibitor 1A,P21)蛋白、Bcl-2相关蛋白(Bcl-2 associated X protein,Bax)蛋白比较:空白对照组<miR-224组<miR-NC组<紫草素组,组间两两比均有统计学意义(P<0.05)。

结论

紫草素可降低鼻咽癌患者miR-224表达,对细胞的增殖、迁移、侵袭起到抑制作用,并对其凋亡起到诱导作用。

紫草素  /  miR-224  /  鼻咽癌  /  增殖  /  迁移  /  侵袭  /  凋亡
Objective

To investigate the effect of shikonin on the cell proliferation,migration,invasion and apoptosis of nasopharyngeal carcinoma(NPC)cells by regulating miR-224 expression.

Methods

Thirty NPC patients treated in the hospital from January 2023 to March 2024 were selected and underwent surgery.The adjacent and cancerous tissues were removed during the surgery.The normal cultured human SUNE-1 cells were recorded as the blank control group,those treated with shikonin were designated as the shikonin group.Those treated with shikonin and transfected with miR-NC and miR-224 mimetics were designated as the miR-NC and miR-224 groups.The expression of miR-224 in each group was compared,and the effects of shikonin on cell proliferation,migration,invasion and apoptosis were observed by regulating miR-224 expression.

Result

The expression of miR-224 in NPC tissue was(3.23±0.16),which was higher than that(1.09±0.07)in adjacent tissues(P<0.05). Comparison of miR-224 expression among the groups:shikonin+miR-224 group>blank control group>shikonin+miR-NC group>shikonin group,and the pairwise comparisons among groups were statistically significant(P<0.05). Comparison of optical density(OD)value,number of migrating cells and number of invading cells among the groups:blank control group>miR-224 group>miR-NC group>shikonin group. Comparison of apoptosis rate among the groups:blank control group<miR-224 group<miR-NC group<shikonin group.There were statistically significant pairwise comparisons among groups(P<0.05). Comparison of CyclinD1 protein,matrix metalloproteinase2(MMP-2)protein,MMP-9 protein and B-cell lymphoma-2(Bcl-2)protein among the groups:blank control group>miR-224 group>miR-NC group>shikonin group. Comparison of cyclin-dependent kinase inhibitor 1A(p21)protein and Bcl-2 associated X protein(Bax)protein among the groups:blank control group<miR-224 group<miR-NC group<shikonin group.There were statistically significant pairwise comparisons among groups(P<0.05).

Conclusion

Shikonin can reduce the expression of miR-224 in NPC patients,inhibit the cell proliferation,migration and invasion,and induce apoptosis.

shikonin  /  miR-224  /  nasopharyngeal carcinoma  /  proliferation  /  migration  /  attack  /  apoptosis
李群真, 李军, 王培, 荣婷, 高亚娜, 张蓉, 苗忠义. 紫草素通过调控miR-224表达对鼻咽癌细胞增殖、迁移、侵袭及凋亡的影响研究. 中华中医药学刊, 2025 , 43 (8) : 88 -91 . DOI: 10.13193/j.issn.1673-7717.2025.08.019
Qunzhen LI, Jun LI, Pei WANG, Ting RONG, Yana GAO, Rong ZHANG, Zhongyi MIAO. Effect of Shikonin on Cell Proliferation,Migration,Invasion and Apoptosis of NPC Cells by Regulating miR-224 Expression[J]. Chinese Archives of Traditional Chinese Medicine, 2025 , 43 (8) : 88 -91 . DOI: 10.13193/j.issn.1673-7717.2025.08.019
鼻咽癌是头颈部的恶性肿瘤,数据资料显示,鼻咽癌手术放化疗后,仍然还有10%~15%的鼻咽癌患者会发生转移或者是复发,且鼻咽癌患者术后5年的生存率约为40%~50%[1-2]。紫草素是萘醌色素,从紫草中提取而来,不仅具有增强免疫力、抗炎等作用,还具有抗癌活性[3-5]。有研究表明,紫草素能够靶向PKM2,进而对PHD3/HIF-1α复合物起到调控作用,致使肝癌细胞发生凋亡[6]。miR-224在机体内广泛分布,在不同的癌症患者中呈不同的表达,miR-224异常和肿瘤的发生以及发展,以及患者的预后有关。研究发现,miR-224在卵巢癌患者中呈高表达,低表达的miR-224卵巢癌患者生存时间长于低表达的miR-224患者,miR-224可靶向调控TNRC6A,调节卵巢癌细胞活性,在细胞凋亡中起到重要作用[7]。但是目前对于miR-224表达是否能够作为紫草素靶向治疗鼻咽癌还尚不完全清楚,基于此,本文研究紫草素通过调控miR-224表达对鼻咽癌细胞的影响,为其治疗鼻咽癌提供辅助参考依据。
选取在我院诊治的鼻咽癌患者30例开展研究,时间点为2023年1月—2024年3月,年龄38~77岁,平均(59.93±7.91)岁,男20例(66.67%),女10例(33.33%)。纳入标准:①经病理确诊为鼻咽癌;②均初次开展规范化治疗;③临床资料完整。排除标准:①其他方面的肿瘤者;②患有影响miR-224表达的疾病者。
将正常培养的人鼻咽癌SUNE-1细胞的记为空白对照组,将人鼻咽癌SUNE-1细胞(源自广州龙龙生物)加入到培养基(DMEM,源自美国Gibco)中,培养基中含有紫草素(规格:10 mg,纯度:>98%,源自上海钰博生物),开展培养,培养的时间为24 h,记为紫草素组,在含有紫草素的培养基中,将进行miR-NC转染的记为miR-NC组,将miR-224 mimics转染的记为miR-224组,开展培养,培养的时间均为24 h。
SUNE-1细胞处理完成后,取出癌和癌旁组织,和细胞(SUNE-1)一起开展研磨处理,加入Trizol试剂,试剂的剂量为1 mL,对总RNA开展提取,并监测其浓度,取出RNA,长度为2 mL,开展逆转录,再进行cDNA的合成,在cDNA中,将DEPC水加入,使其稀释至20倍,采用qRT-PCR法对miR-224表达开展检测。
按照分组处理好SUNE-1细胞,取100 μL,将其接种到96孔板,在每孔中加入CCK-8溶液(源自碧云天生物)10μL,在室温进行2 h的孵育。对细胞吸光度(optical density,OD)值进行检测。
SUNE-1细胞处理完成后,接种到孔板中,孔板24孔,细胞数为2.5×104个,培养完成后,对细胞凋亡进行检测,采用的方法为流式细胞仪。
①侵袭实验:SUNE-1细胞处理完成后,将细胞接种至小室的上层,细胞的个数为1×106 个/mL,小室采用Matrigel基质胶包被,采用培养基(没有血清)对其开展培养,在小室的下层,将细胞培养液(正常的)加入,开展培养,培养的时间为24 h,对上层细胞(小室)进行擦拭,采用的是棉签(无菌),再用多聚甲醛(其浓度为4%),进行20 min的固定,采用结晶紫(浓度为0.1%),对SUNE-1细胞(在小室的下层),开展染色,染色的时间为15 min,查看侵袭的细胞数。②迁移实验:细胞接种的地方为小室的上层,方法同上。均各做3次实验。
SUNE-1细胞处理完成后,开展离心处理后,去除上清液,进行清洗,清洗液采用PBS,再次去除上清液,对细胞开展裂解,采用的裂解液为RIRP,回收上清,采用BCA蛋白溶度的方法,测定细胞的总蛋白,采用GAPHD作为内参,进行Western blot检测,兔抗人的细胞周期蛋白1(CyclinD1)、细胞周期依赖性蛋白激酶抑制因子1A(cyclin-dependent kinase inhibitor 1A,P21)、基质金属蛋白酶2(matrix metalloproteinase2,MMP-2)、MMP-9、B淋巴细胞瘤-2(Bcell lymphoma-2,Bcl-2)、Bcl-2相关蛋白(Bcl-2 associated X protein,Bax)的一抗和二抗均源自美国SantaCruz,采用Quantityone软件对条带灰度值进行检测。
以SPSS 22.0分析所有数据,计数资料表示为例(%);计量资料表示为(),4组比较开展单因素方差分析,两组之间开展LSD-t法。P<0.05,差异有统计学意义。
和癌旁组织的miR-224表达(1.09±0.07)相比,鼻咽癌组织的miR-224表达(3.23±0.16)更高(P<0.05),见图1。
miR-224组、miR-NC组、紫草素组、空白对照组的miR-224表达分别为(2.29±0.13)、(1.02±0.11)、(0.43±0.09)、(1.15±0.13);和空白对照组相比,miR-NC组、紫草素组miR-224表达更低(P<0.05),miR-224组miR-224表达更高(P<0.05);和紫草素组相比,miR-224组、miR-NC组miR-224表达更高(P<0.05);和miR-NC组相比,miR-224组miR-224表达更高(P<0.05)。
和空白对照组相比,miR-224组、miR-NC组、紫草素组OD值、迁移细胞数、侵袭细胞数更低(P<0.05),miR-224组、miR-NC组、紫草素组凋亡率更高(P<0.05);和紫草素组相比,miR-224组、miR-NC组OD值、迁移细胞数、侵袭细胞数更高(P<0.05),miR-224组、miR-NC组凋亡率更低(P<0.05);和miR-NC组相比,miR-224组OD值、迁移细胞数、侵袭细胞数更高(P<0.05),miR-224组凋亡率更低(P<0.05)。见表1。
和空白对照组相比,miR-224组、miR-NC组、紫草素组CyclinD1蛋白、MMP-2蛋白、MMP-9蛋白、Bcl-2蛋白更低(P<0.05),miR-224组、miR-NC组、紫草素组p21蛋白、Bax蛋白更高(P<0.05);和紫草素组相比,miR-224组、miR-NC组CyclinD1蛋白、MMP-2蛋白、MMP-9蛋白、Bcl-2蛋白更高(P<0.05),miR-224组、miR-NC组p21蛋白、Bax蛋白更低(P<0.05);和miR-NC组相比,miR-224组CyclinD1蛋白、MMP-2蛋白、MMP-9蛋白、Bcl-2蛋白更高(P<0.05),miR-224组p21蛋白、Bax蛋白更低(P<0.05)。见表2。
在耳鼻咽喉方面的癌症中,鼻咽癌占首位,患者临床主要呈现为鼻出血、回缩性血涕等,最终可能会引发吞咽障碍以及听力受损等[8-9]。在中医学中,鼻咽癌属于“鼻衄”“鼻疽”等范畴,是因肝胆热毒和肺热痰火上扰导致。紫草素是从紫草中提取而来,味咸、甘,性寒凉,具有解毒、透疹、凉血的作用,可应用于治疗疮疡、血热毒盛、麻疹不透等,具有抗病毒、抗炎以及抗肿瘤等功效[10-13]。凋亡是细胞死亡的形式,但是癌细胞存在细胞凋亡抗性,因此抑制癌细胞的增殖,并促进癌细胞的凋亡,是目前临床治疗癌症的重要靶点[14-16]。有研究表明,紫草素在鼻咽癌的抗肿瘤中起到显著效果,可通过不同靶点以及途径对细胞的侵袭和迁移起到抑制作用,是治疗鼻咽癌的潜力型药物[17]。
miR-224是微小RNA,不仅在肿瘤的发生以及发展中发挥重要作用,也在肿瘤的治疗中起到重要作用。张慧萍等[18]研究显示,miR-224在宫颈癌中呈高表达。宗彦红等[19]研究发现,在肝癌组织和血浆中,miR-224呈显著高表达,且miR-224表达和肝癌预后不良呈显著相关性,敲低miR-224表达,能够对肝癌HepG2细胞的克隆形成、侵袭起到抑制作用。本文研究中,鼻咽癌组织中miR-224表达为(3.23±0.16),和癌旁组织的(1.09±0.07)相比更高,说明鼻咽癌患者miR-224呈高表达。细胞的增殖、迁移、侵袭以及凋亡的过程复杂,且相互关联,能够维持疾病的发展。因此可通过研究该过程的机制,以研究其在不同生物背景之下的应用效果。梁国新等[20]研究表明,过表达的miR-224-5p会通过PI3K/AKT/FoxO1轴,对抗氧化基因SOD2的表达进行上调,进而缓解H/R诱导的H9C2细胞的氧化应激程度,最终减少细胞的凋亡。张姗等[21]研究表明,过表达的miR-224-5p通过靶向SMAD5,从而对弥漫大B细胞淋巴瘤的U2932细胞的增殖起到抑制作用,并且还能够诱导U2932细胞的凋亡。WANG G等[22]研究表明,LncRNA HCG11能够对miR-224-3p的表达起到抑制作用,且还能够对非小细胞肺癌的增殖起到抑制作用,并促进细胞的凋亡。谢瑜等[23]研究表明,在DLBCL的进展中,miR-224起到重要作用,miR-224能够通过靶向抑制PIK3CD,进而对HBL1细胞(DLBCL细胞系)的增殖以及侵袭起到抑制作用。本文研究中,miR-224表达比较:miR-224组>空白对照组>miR-NC组>紫草素组,说明过表达的miR-224,可对紫草素作用在鼻咽癌细胞的生物学行为起到拮抗作用。
李世玲等[24]研究表明,紫草素可对非小细胞肺癌细胞的增殖以及迁移起到抑制作用。刘亚楠等[25]研究表明,紫草素可对子宫内膜癌细胞的存活起到抑制作用,并对细胞凋亡起到诱导作用,其机制和HNF1A-AS1/miR-20b-5p轴的调控有关。本文研究中,OD值、迁移细胞数、侵袭细胞数及CyclinD1蛋白、MMP-2蛋白、MMP-9蛋白、Bcl-2蛋白比较:空白对照组>miR-224组>miR-NC组>紫草素组,凋亡率及p21蛋白、Bax蛋白比较:空白对照组<miR-224组<miR-NC组<紫草素组,说明紫草素应用于鼻咽癌患者,可对其细胞的增殖、迁移和侵袭起到抑制作用,并对其细胞凋亡起到诱导作用。
综上所述,在鼻咽癌患者的癌组织中,miR-224表达升高,紫草素可降低鼻咽癌患者miR-224表达,对细胞的增殖、迁移、侵袭起到抑制作用,并对其凋亡起到诱导作用,表明紫草素可通过调控miR-224表达进而发挥对鼻咽癌的抗肿瘤作用。
  • 国家重点研发计划中医药现代化研究重点专项(2020YFC1106000)
  • 河北省中医药管理局科研计划项目(2023028)
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2025年第43卷第8期
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doi: 10.13193/j.issn.1673-7717.2025.08.019
  • 首发时间:2026-10-30
  • 出版时间:2025-08-10
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国家重点研发计划中医药现代化研究重点专项(2020YFC1106000)
河北省中医药管理局科研计划项目(2023028)
作者信息
    1.河北省中医院,河北 石家庄 050011
    2.石家庄市中医院,河北 石家庄 050000

通讯作者:

李军(1976-),男,副主任医师,硕士,研究方向:鼻科疾病的中西医结合治疗。E-mail:。
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2种不同金属材料的力学参数
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genus
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species
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属
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species
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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
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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