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Characterization of flounder (Paralichthys olivaceus) FoxD5 and its function in regulating myogenic regulatory factor
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作者 谭训刚 张玉青 +2 位作者 孙威 张培军 徐永立 《Chinese Journal of Oceanology and Limnology》 SCIE CAS CSCD 2012年第2期286-294,共9页
As one member of winged helix domain transcription factors, FoxD5 was reported to be a trunk organizer. Recent study showed that zebrafish foxd5 is expressed in the somites. To further understand the function of FoxD5... As one member of winged helix domain transcription factors, FoxD5 was reported to be a trunk organizer. Recent study showed that zebrafish foxd5 is expressed in the somites. To further understand the function of FoxD5 in fish muscle development, the FoxD5 gene was isolated from flounder. Its expression pattern was analyzed by in situ hybridization, while its function in regulating myogenic regulatory factor, MyoD, was analyzed by ectopic expression. It showed that flounder FoxD5 was firstly expressed in the tailbud, adaxial cells, and neural plate of the head. In flounder embryo, FoxD5 is expressed not only in forebrain but also in somite cells that will form muscle in the future. When flounder FoxD5 was over-expressed in zebrafish by microinjection, the expression of zebrafish MyoD in the somites was reduced, suggesting that FoxD5 is involved in myogenesis by regulating the expression of MyoD. 展开更多
关键词 FLOUNDER foxd5 MUSCLE OVER-EXPRESSION in situ hybridization myogenic regulatory factor
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LINC01355通过miR-545-5p/FOXD1信号通路对口腔鳞状细胞癌细胞增殖、凋亡和侵袭的影响 被引量:1
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作者 高静 魏校通 +2 位作者 李星晨 闫威 王浩 《中国医科大学学报》 北大核心 2025年第3期238-245,共8页
目的探讨LINC01355通过miR-545-5p/叉头盒D1(FOXD1)信号通路对口腔鳞状细胞癌(OSCC)细胞增殖、凋亡和侵袭的影响。方法体外培养人OSCC细胞系Cal-27,随机分为对照组、转染LINC01355 siRNA(si-LINC01355)组、转染LINC01355过表达质粒(pc-L... 目的探讨LINC01355通过miR-545-5p/叉头盒D1(FOXD1)信号通路对口腔鳞状细胞癌(OSCC)细胞增殖、凋亡和侵袭的影响。方法体外培养人OSCC细胞系Cal-27,随机分为对照组、转染LINC01355 siRNA(si-LINC01355)组、转染LINC01355过表达质粒(pc-LINC01355)组、转染LINC01355 siRNA阴性对照+miR-545-5p阴性对照+空载质粒(si-NC+miR-545-5p-NC+pc-NC)组、转染LINC01355 siRNA+miR-545-5p抑制剂(si-LINC01355+miR-545-5p inhibitor)组。转染后实时定量PCR检测各组细胞LINC01355、miR-545-5p及FOXD1表达;转染后的Cal-27细胞通过皮下接种构建各组移植瘤裸鼠模型,测量移植瘤生长情况;CCK-8法、流式细胞术、Transwell实验分别检测各组细胞增殖、凋亡和侵袭情况;免疫组织化学染色检测细胞上皮-间质转化(EMT)相关蛋白Vimentin、E-cadherin表达;Western blotting检测细胞增殖相关蛋白[增殖细胞核抗原(PCNA)、C-myc]、凋亡相关蛋白[切割型胱天蛋白酶-3(cleaved caspase-3)、BCL-2相关X蛋白(Bax)]与FOXD1表达。双萤光素酶报告实验鉴定LINC01355与miR-545-5p/FOXD1信号通路的靶向关系。结果与对照组比较,si-LINC01355组LINC01355、FOXD1 mRNA表达,增殖活性,侵袭数量,Vimentin蛋白阳性表达,PCNA、C-myc与FOXD1蛋白表达,移植瘤体积均降低(均P<0.05);而miR-545-5p表达,细胞凋亡率,cleaved caspase-3、Bax蛋白表达,E-cadherin蛋白阳性表达均升高(均P<0.05)。pc-LINC01355组各指标变化趋势与si-LINC01355组相反。与si-LINC01355组比较,si-LINC01355+miR-545-5p inhibitor组LINC01355、FOXD1 mRNA表达,增殖活性,侵袭数量,Vimentin蛋白阳性表达,PCNA、C-myc与FOXD1蛋白表达,移植瘤体积均增加(均P<0.05),而miR-545-5p表达、细胞凋亡率、cleaved caspase-3与Bax蛋白表达、E-cadherin蛋白阳性表达均降低(均P<0.05)。Cal-27细胞中LINC01355可靶向下调miR-545-5p表达,且miR-545-5p可靶向下调FOXD1表达。结论LINC01355可通过调控miR-545-5p/FOXD1信号通路促进OSCC细胞增殖和侵袭,抑制细胞凋亡。 展开更多
关键词 口腔鳞状细胞癌 LINC01355 miR-545-5p/FOXD1信号通路 增殖 凋亡 侵袭
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