来自杂志 Gene 的文献。
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1.
龙海晨
(2024-11-07 13:24):
#paper Galea GL, Paradise CR, Meakin LB, Camilleri ET, Taipaleenmaki H, Stein GS, Lanyon LE, Price JS, van Wijnen AJ, Dudakovic A. Mechanical strain-mediated reduction in RANKL expression is associated with RUNX2 and BRD2. Gene. 2020 Dec;763S:100027. doi: 10.1016/j.gene.2020.100027. Epub 2020 Jan 16. PMID: 34493364.这是一篇研究机械应变与成骨活动的文章。机械负荷相关的应变触发成骨细胞形成骨,同时抑制破骨细胞的骨吸收,从而开启骨形成和骨吸收的过程。骨细胞可能通过分泌硬化素(SOST)(抑制成骨细胞)和表达核因子-κB配体受体激活剂。(RANKL/TNFSF11)来生成破骨细胞协调这一过程。机械应变会降低 SOST 和 RANKL 表达。RUNX2 敲低会增加 SOST 水平。
RUNX2 促进机械应变介导的 RANKL 抑制。BRD2 表达受机械应变和 RUNX2 调节。
Gene,
2020-12.
DOI: 10.1016/j.gene.2020.100027
机械菌株介导的 RANKL 表达降低与 RUNX2 和 BRD2 相关
Abstract:
No abstract available.
2.
龙海晨
(2022-05-12 11:23):
#paper Artesunate exhibits synergistic anti-cancer effects with cisplatin on lung cancer A549 cells by inhibiting MAPK pathway
PMID: 32898605 GENE杂志Gene 2021 Jan 15;766:145134.
doi: 10.1016/j.gene.2020.145134. Epub 2020 Sep 6.
DOI: 10.1016/j.gene.2020.145134
文章研究了青蒿琥酯(Artesunate,ART)与顺铂(cisplatin,CIS)联合发挥抗肺癌作用。使用A549肺癌细胞系进行研究。发现ART加大剂量获延长使用时间均能抑制细胞增殖。且ART与CIS联合使用,抑癌效果要显著强于单独用ART获单独用CIS,使用裸鼠进行动物实验也得到了同样结果。并证明,联合效果是通过P38/JNK/ERK MAPK信号通路发挥作用。
Abstract:
BACKGROUND: Artesunate (ART) has been used extensively as anti-malarial drugs worldwide. Besides, it has also been reported to have anti-cancer activities. This study was aimed to explore the anti-cancer activity …
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BACKGROUND: Artesunate (ART) has been used extensively as anti-malarial drugs worldwide. Besides, it has also been reported to have anti-cancer activities. This study was aimed to explore the anti-cancer activity of ART in combination with cisplatin (CIS) on A549 cells.METHODS: Cells were cultured with different concentrations of ART and/or CIS for 24, 48, or 72 h to test the anti-proliferative effects by CCK-8 assay. Colony formation assay and EdU staining were also performed. TUNEL staining was used to illustrate the morphologic changes. Cell cycle and apoptosis were determined by flow cytometry assay, and Western blot analysis was conducted to detect the expression of apoptosis- and proliferation-related proteins. Caspase activities were determined by colorimetric assay kit. Moreover, the synergistic effect of ART with CIS in A549 cell xenograft model was also determined.RESULTS: ART significantly inhibited cell proliferation in dose- and time-dependent manners. Collectively, the combination treatment remarkably decreased colony formation rates and increased the rates of TUNEL-positive cells compared with mono-treatment. Mechanistically, the combination treatment influenced the expression of Bcl-2, Bax, p-P53, Caspase-3/7, Caspase-9, CyclinB1, P34, P21, and synergistically regulated the activity of P38/JNK/ERK1/2 MAPK pathway. In mice A549 xenograft tumors, the combination strategy significantly increased the anti-cancer efficacy of ART and CIS alone, consistent with the in vitro observations.CONCLUSIONS: ART exhibited significant anti-tumor effect on A549 cells and this efficiency could be enhanced by combination with CIS.
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