首页|lncRNA SNHG 15调控miR-95-3p对乳腺癌细胞增殖、凋亡的影响

lncRNA SNHG 15调控miR-95-3p对乳腺癌细胞增殖、凋亡的影响

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目的 探究长链非编码 RNA(long non-coding RNA,lncRNA)核仁小 RNA 宿主基因 15(small nucleolar RNA host gene 15,SNHG 15)调控微RNA95-3p(microRNA 95-3p,miR-95-3p)对乳腺癌细胞增殖、凋亡的影响.方法 将乳腺癌细胞分为对照组、敲减组、干扰组、共转染组,体外培养人乳腺癌细胞系MDA-MB-231.测定SNHG 15 mRNA、miR-95-3p mRNA相对表达量;使用噻唑兰(methylthiazolyldiphenyl-tetrazolium bromide,MTT)法检测乳腺癌细胞增殖能力;流式细胞仪检测乳腺癌细胞凋亡情况;划痕试验检测乳腺癌细胞迁移能力;Transwell侵袭实验测定乳腺癌细胞侵袭个数;采用Western blot法测定半胱氨酸蛋白酶3(caspase-3)、B淋巴细胞瘤-2(B-cell lymphoma-2,Bcl-2)、Bcl-2相关X蛋白(Bcl-2 associated X protein,Bax)相对表达量.结果 与对照组比较,敲减组 SNHG 15 mRNA、miR-95-3p mRNA 相对表达量及增殖能力、增殖率、迁移能力、侵袭个数、Bcl-2蛋白表达下降;凋亡情况、凋亡率、caspase-3、Bax表达升高(P<0.05).与敲减组、干扰组比较,共转染组SNHG 15 mRNA、miR-95-3p mRNA相对表达量及增殖能力、增殖率、迁移能力、侵袭个数、Bcl-2蛋白表达升高;凋亡情况、凋亡率、caspase-3、Bax表达降低(P<0.05).与干扰组比较,共转染组SNHG 15 mRNA、miR-95-3p mRNA相对表达量及增殖能力、增殖率、迁移能力、侵袭个数、Bcl-2表达升高,凋亡情况、凋亡率、caspase-3、Bax蛋白表达降低(P<0.05).结论 lncRNA SNHG 15可通过调控miR-95-3p表达影响乳腺癌细胞的增殖与凋亡,与乳腺癌细胞的发生、发展呈正相关.
Effect of lncRNA SNHG 15 in regulating miR-95-3p on the proliferation and apoptosis of breast cancer cells
Objective To explore the effect of long non-coding RNA(long non-coding RNA,lncRNA)small RNA host gene 15(small nucleolar RNA host gene 15,SNHG 15)regulating microRNA 95-3p(miR-95-3p)on breast cancer cell proliferation and apoptosis.Methods Breast cancer cells were divided into control group,knockdown group,interference group and co-transfection group.Human breast cancer cell line MDA-MB-231 was cultured in vitro.Measure the relative expression levels of SNHG 15 mRNA and miR-95-3p mRNA;Methylthiazolyldiphenyl-tetrazolium bromide(MTT)was used to detect the proliferation ability of breast cancer cells;The apoptosis of breast cancer cells was detected by flow cytometry;The migration ability of breast cancer cells was detected by scratch test;Transwell invasion test was used to measure the number of breast cancer cells invaded;Western blot was used to determine the relative expression levels of caspase-3,B-cell lymphoma-2(Bcl-2),and Bcl-2 associated X protein(Bax).Results Compared with control group,the relative expression level of SNHG 15 mRNA and miR-95-3p mRNA,proliferation ability,proliferation rate,migration ability,number of invasion,Bcl-2 protein expression were decreased,but the apoptosis status,apoptosis rate,caspase-3 and Bax expression were increased in knockdown group(P<0.05).Compared with knockdown group and interference group,the relative expression level of SNHG 15 mRNA and miR-95-3p mRNA,proliferation capacity,proliferation rate,migration capacity,number of invasion,Bcl-2 protein expression were increased,but apoptosis status,apoptosis rate,caspase-3 and Bax expression were decreased in co-transfection group(P<0.05).Compared with interference group,the relative expression level of SNHG 15 mRNA and miR-95-3p mRNA,proliferation ability,proliferation rate,migration ability,number of invasion,Bcl-2 protein expression were increased,but apoptosis status,apoptosis rate,caspase-3 and Bax expression were decreased in co-transfection group(P<0.05).Conclusion lncRNA SNHG 15 can affect the proliferation and apoptosis of breast cancer cells by regulating miR-95-3p expression,and is positively associated with the occurrence and development of breast cancer cells.

Long non-coding nucleolar small RNA host gene 15Long non-coding RNAmicroRNA 95-3pBreast cancerProliferationApoptosi

孙凯廷、池益利

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温州市中西医结合医院肿瘤科,浙江温州 325000

长链非编码核仁小RNA宿主基因15 长链非编码RNA 微小RNA95-3p 乳腺癌 增殖 凋亡

2024

中国现代医生
中国医学科学院

中国现代医生

影响因子:1.571
ISSN:1673-9701
年,卷(期):2024.62(21)
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