胰腺癌
基因敲除
乙酰化
车站3
癌症研究
肿瘤微环境
下调和上调
细胞生长
细胞培养
化学
免疫系统
生物
癌细胞
癌症
分子生物学
细胞生物学
免疫学
信号转导
生物化学
基因
遗传学
作者
Yuan He,Pengyong Han,Chuang Chen,Shuzhe Xie,Huiqing Zhang,Yingming Song,Hao Hu,Qiang Zhao,Changhong Lian
标识
DOI:10.1038/s41417-021-00382-w
摘要
Accumulating research implicated that circular RNAs exhibited significant roles in cancer development. Nonetheless, the role regarding circPTPN22 in pancreatic cancer remains unclear. Expression of circPTPN22 in pancreatic cancer cell lines and normal cells was determined with quantitative real-time PCR (qRT-PCR). Cell counting kit-8 assay and colony formation assay were used to measure the proliferation of pancreatic cancer cells. RNA immunoprecipitation and Western blot were employed for investigation the binding between circPTPN22 and STAT3. circPTPN22 expression was highly upregulated in pancreatic cancer tissues and cell lines. Knockdown of circPTPN22 inhibited cell proliferation and attenuates pancreatic cancer immune microenvironment. Furthermore, STAT3 acetylation was involved in these effects. circPTPN22 promoted STAT3 acetylation via inhibiting STAT3/SIRT1 interaction. circPTPN22 attenuates pancreatic cancer immune microenvironment by promoting STAT3 acetylation via inhibiting STAT3/SIRT1 interaction.
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