文章摘要
高晶晶,孙志涛,姜辉,等.藏红花素抑制音猬因子信号通路对结直肠癌细胞恶性生物学行为的影响[J].安徽医药,2024,28(2):224-229.
藏红花素抑制音猬因子信号通路对结直肠癌细胞恶性生物学行为的影响
Influence of crocin on the malignant biological behavior of colorectal cancer cells by inhibiting Shh signaling pathway
  
DOI:10.3969/j.issn.1009-6469.2024.02.004
中文关键词: 秋水仙属  人结直肠癌细胞 SW620  音猬因子信号通路  恶性生物学行为
英文关键词: Colchicum  Human colorectal cancer cell SW620  Sonic hedgehog signaling pathway  Malignant biological behavior
基金项目:沧州市科技局重点研发项目( 204106010)
作者单位
高晶晶 沧州市人民医院 胃肠外科河北沧州 061000 
孙志涛 沧州市人民医院 胃肠外科河北沧州 061000 
姜辉 沧州市人民医院肛肠外科河北沧州 061000 
张宝玉 沧州市人民医院神经外科河北沧州 061000 
肖伟 沧州市人民医院 胃肠外科河北沧州 061000 
周国庆 沧州市人民医院 胃肠外科河北沧州 061000 
宋东旭 沧州市人民医院 胃肠外科河北沧州 061000 
张亚玲 沧州市人民医院 胃肠外科河北沧州 061000 
马红艳 沧州市人民医院病理科河北沧州 061000 
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中文摘要:
      目的探究藏红花素抑制音猬因子(Shh)信号通路对结直肠癌细胞恶性生物学行为的影响。方法 2021年 1月至 2022年 7月体外培养人结直肠癌细胞 SW620,使用不同浓度( 5、10、20、40、60、80 mg/L)的藏红花素处理 SW620细胞 24 h后, CCK-8法检测藏红花素对 SW620细胞的细胞毒性作用。将 SW620细胞分别用不同剂量藏红花素( 10、20、40 mg/L,藏红花素 L/M/H组)、 40 mg/L藏红花素 +1 μmol/L Purmorphamine(藏红花素 H+Shh通路激活剂组)、1 μmol/L Purmorphamine(Shh通路激活剂组)处理,另设置未经处理的对照( Control)组,检测 SW620细胞增殖、凋亡、迁移和侵袭能力以及 Shh信号通路相关蛋白 Shh、平滑蛋白( Smo)、神经胶质瘤相关癌基因 -1(Gli-1)表达。结果藏红花素以剂量依赖性方式降低 SW620细胞活力。与对照组相比, Shh通路激活剂组 SW620细胞活力升高,克隆形成数、划痕面积愈合率、侵袭数、 Shh(1.47±0.09比 1.27±0.08)、 Smo(1.38±0.12比 1.15±0.09)、 Gli-1(1.25±0.09比 0.98±0.07)蛋白表达增加,细胞凋亡率减少( P<0.05),藏红花素 L组、藏红花素 M组、藏红花素 H组 SW620细胞活力下降,克隆形成数、划痕面积愈合率、侵袭数减少,凋亡率增加, Shh(1.07±0.12、0.85±0.11、0.52±0.08比 1.32±0.14)、 Smo(0.96±0.11、0.72±0.08、0.43±0.06比 1.19±0.12)、 Gli-1(0.76±0.09、0.61±0.09、0.37±0.06比 0.96±0.11)蛋白表达减少(P<0.05);与藏红花素 H组相比,藏红花素 H+Shh通路激活剂组 SW620细胞活力升高,克隆形成数、划痕面积愈合率、侵袭数增加,凋亡率减少, Shh(0.84±0.08比 0.52±0.08)、 Smo(0.81±0.09比 0.43±0.06)、 Gli-1(0.70±0.08比 0.37±0.06)蛋白表达增加(P<0.05)。结论藏红花素可抑制 SW620细胞增殖、迁移和侵袭,促进其凋亡,可能与抑制 Shh信号通路有关。
英文摘要:
      Objective To explore the influence of crocin on the malignant biological behavior of colorectal cancer cells by inhibitingthe sonic hedgehog (Shh) signaling pathway.Methods From January 2021 to July 2022,Human colorectal cancer cells SW620 werecultured in vitro and treated with crocin at different concentrations (5,10,20,40,60,80 mg/L) for 24 h.The cytotoxic effects of crocin onSW620 cells were detected by CCK-8 assay. SW620 cells were treated with different doses of crocin (10, 20, 40 mg/L, crocin L/M/Hgroup), 40 mg/L crocin + 1 μmol/L Purmorphamine (crocin H+Shh pathway activator group), 1 μmol/L Purmorphamine (Shh pathwayactivator group), and an untreated control group was set up. The ability of proliferation, apoptosis, migration and invasion of SW620cells and the expression of Shh signaling pathway related proteins Shh, smooth protein (Smo) and glioma associated oncogene-1 (Gli-1) were detected.Results Crocin decreased SW620 cell viability in a dose-dependent manner. Compared with the Control group, the via.bility of SW620 cells in the Shh pathway activator group was increased, the number of clone formation, the healing rate of scratch area,the number of invasion, the expression of Shh (1.47±0.09 vs. 1.27±0.08), Smo (1.38±0.12 vs. 1.15±0.09) and Gli-1 (1.25±0.09 vs. 0.98± 0.07) proteins were increased, and the apoptosis rate was decreased (P<0.05). the viability of SW620 cells in the crocin L group, thecrocin M group and the crocin H group decreased, the number of colonies, the healing rate of the scratch area, and the number of inva.sion decreased, the apoptosis rate increased, and the protein expression of Shh (1.07±0.12, 0.85±0.11, 0.52±0.08 vs. 1.32±0.14), Smo (0.96±0.11, 0.72±0.08, 0.43±0.06 vs. 1.19±0.12) and Gli-1 (0.76±0.09, 0.61±0.09, 0.37±0.06 vs. 0.96±0.11) decreased (P<0.05); com.pared with the crocin H group, the viability of SW620 cells in the crocin H+Shh pathway activator group increased, the number of colo.nies, the healing rate of the scratch area, and the number of invasion increased, the apoptosis rate decreased, and the protein expression of Shh (0.84±0.08 vs. 0.52±0.08), Smo (0.81±0.09 vs. 0.43±0.06) and Gli-1 (0.70±0.08 vs. 0.37±0.06) increased (P<0.05).Conclusion Crocin can inhibit the proliferation, migration and invasion of SW620 cells and promote their apoptosis, which may be related to the in.hibition of Shh signaling pathway.
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