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微小RNA-15a-3p通过靶向谷胱甘肽过氧化物酶GPX4调控结直肠癌中的铁死亡。

MiR-15a-3p regulates ferroptosis via targeting glutathione peroxidase GPX4 in colorectal cancer.

作者信息

Liu Liurong, Yao Huihui, Zhou Xin, Chen Junjie, Chen Guoliang, Shi Xinyu, Wu Guanting, Zhou Guoqiang, He Songbing

机构信息

Department of General Surgery, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.

Department of General Surgery, Yancheng Third People's Hospital, Yancheng, Jiangsu, China.

出版信息

Mol Carcinog. 2022 Mar;61(3):301-310. doi: 10.1002/mc.23367. Epub 2021 Nov 2.

Abstract

Colorectal cancer (CRC) is the second most common cancer-related deaths throughout the world. Ferroptosis is a recently regulated form of cell death, lately gains attention. MicroRNA-15a-3p (miR-15a-3p) plays a regulatory role in various kinds of cancers. However, the role of miR-15a-3p in cellular ferroptosis is still unclear. Here, we aimed to clarify whether miR-15a-3p could regulate the ferroptosis of CRC. Here we identified miR-15a-3p positively regulates ferroptosis via directly targeting glutathione peroxidase glutathione peroxidase 4 (GPX4) in CRC. Overexpression of miR-15a-3p repressed GPX4 through binding to the 3'-untranslated region of GPX4, resulting in increased reactive oxygen species level, intracellular Fe level, and malondialdehyde accumulation in vitro and in vivo. Correspondingly, suppression of miR-15a-3p reduced the sensitivity of CRC cells to erastin and GPX4. Taken together, these data demonstrate that miR-15a-3p regulates ferroptosis through targeting GPX4 in CRC cells, illustrating the novel role of microRNA in ferroptosis.

摘要

结直肠癌(CRC)是全球第二大常见的癌症相关死亡原因。铁死亡是一种最近被调控的细胞死亡形式,近来受到关注。微小RNA-15a-3p(miR-15a-3p)在各种癌症中发挥调节作用。然而,miR-15a-3p在细胞铁死亡中的作用仍不清楚。在此,我们旨在阐明miR-15a-3p是否能调节结直肠癌的铁死亡。在这里,我们发现miR-15a-3p通过直接靶向结直肠癌中的谷胱甘肽过氧化物酶4(GPX4)来正向调节铁死亡。miR-15a-3p的过表达通过与GPX4的3'-非翻译区结合来抑制GPX4,导致体外和体内活性氧水平升高、细胞内铁水平升高以及丙二醛积累。相应地,抑制miR-15a-3p降低了结直肠癌细胞对埃拉斯汀和GPX4的敏感性。综上所述,这些数据表明miR-15a-3p通过靶向结直肠癌细胞中的GPX4来调节铁死亡,阐明了微小RNA在铁死亡中的新作用。

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