Histone demethylase JMJD1A in cancer progression and therapeutic resistance.

Histone demethylase JMJD1A in cancer progression and therapeutic resistance.
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DOI:
10.1002/mc.23390
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发表时间:
2022-04
影响因子:
4.6
通讯作者:
Qi J
Qi J
中科院分区:
医学2区
文献类型:
--
作者:
Jeon HY;Ryu H;Pornour M;Qi J

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JMJD1A(也称为 KDM3A)属于组蛋白去甲基酶 JmjC 家族。它专门去除 H3K9 的抑制性单甲基或二甲基标记,从而有助于基因转录的激活。 JMJD1A 在精子发生、代谢、性别决定和干细胞活性等多种生物过程中发挥着关键作用。 JMJD1A 在多种类型的癌症中表达上调,并且可以促进癌症的发生、进展和治疗耐药性。 JMJD1A可以表观遗传调控c-Myc、AR、ER、β-catenin等转录因子的表达或活性。癌细胞中 JMJD1A 的表达和活性可以在转录、转录后和翻译后水平上受到调节。靶向 JMJD1A 可能会抑制致癌转录因子,作为一种潜在的抗癌疗法。
JMJD1A (also called KDM3A) belongs to the JmjC family of histone demethylases. It specifically removes the repressive mono- or di-methyl marks from H3K9 and thus contributes to the activation of gene transcription. JMJD1A plays a key role in a variety of biological processes such as spermatogenesis, metabolism, sex determination and stem cell activity. JMJD1A is upregulated in various types of cancers, and can promote cancer development, progression and therapeutic resistance. JMJD1A can epigenetically regulate the expression or activity of transcription factors such as c-Myc, AR, ER, β-catenin, et al. Expression and activity of JMJD1A in cancer cells can be regulated at transcriptional, post-transcriptional and post-translational levels. Targeting JMJD1A may repress the oncogenic transcription factors as a potential anti-cancer therapy.
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