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首页> 外文期刊>American Journal of Cancer Research >Downregulation of histone demethylase JMJD1C inhibits colorectal cancer metastasis through targeting ATF2
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Downregulation of histone demethylase JMJD1C inhibits colorectal cancer metastasis through targeting ATF2

机译:下调组蛋白脱甲基酶JMJD1C通过靶向ATF2抑制大肠癌转移

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摘要

Colorectal cancer (CRC) is one of the most common malignant gastrointestinal cancers. Metastasis is a major leading of death in patients with CRC and many patients have metastatic disease at diagnosis. However, the underlying molecular mechanisms are still elusive. Here, we showed that JMJD1C was overexpressed in colon cancer tissues compared to normal samples and was positively associated with metastasis and poor prognosis. Silencing JMJD1C strongly inhibits CRC migration and invasion both in vitro and in vivo. Further, we found that knockdown of JMJD1C decreased the protein and mRNA levels of ATF2, mechanistically, and JMJD1C regulated the expression of ATF2 by modulating the H3K9me2 but not H3K9me1 activity. In addition, we further performed some “rescues experiments”. We found that overexpression of ATF2 could reverse the abrogated migration and invasion ability by knockdown of JMJD1C in CRC. Our results demonstrated that an increase of JMJD1C was observed in colon cancer and knockdown of JMJD1C regulated CRC metastasis by inactivation of the ATF2 pathway. This novel JMJD1C/ATF2 signaling pathway may be a promising therapeutic target for CRC metastasis.
机译:大肠癌(CRC)是最常见的恶性胃肠道癌之一。转移是导致CRC患者死亡的主要原因,许多患者在诊断时患有转移性疾病。但是,潜在的分子机制仍然难以捉摸。在这里,我们显示与正常样品相比,JMJD1C在结肠癌组织中过表达,并且与转移和预后不良呈正相关。沉默JMJD1C可以在体内和体外强烈抑制CRC迁移和侵袭。此外,我们发现敲低JMJD1C会从机制上降低ATF2的蛋白质和mRNA水平,并且JMJD1C通过调节H3K9me2而不是H3K9me1活性来调节ATF2的表达。此外,我们还进行了一些“救援实验”。我们发现,ATF2的过表达可以通过敲低CRC中的JMJD1C来逆转废止的迁移和侵袭能力。我们的结果表明,在结肠癌中观察到JMJD1C的增加,并且通过使ATF2途径失活而抑制了JMJD1C调节的CRC转移。这种新颖的JMJD1C / ATF2信号通路可能是CRC转移的有希望的治疗靶标。

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