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一种睾丸特异性长链非编码RNA作为MDM2的转录后调节因子发挥作用,并刺激睾丸生殖细胞肿瘤细胞的凋亡。

A testis-specific lncRNA functions as a post-transcriptional regulator of MDM2 and stimulates apoptosis of testicular germ cell tumor cells.

作者信息

Ito Saya, Ueno Akihisa, Ueda Takashi, Ogura Ryota, Sako Satoshi, Gabata Yusuke, Murashita Junki, Takahashi Hikaru, Ukimura Osamu

机构信息

Department of Urology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto-City, Kyoto, Japan.

出版信息

Cell Death Discov. 2024 Aug 3;10(1):348. doi: 10.1038/s41420-024-02119-8.

DOI:10.1038/s41420-024-02119-8
PMID:39097584
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11297958/
Abstract

Germ cells preferentially induce apoptosis in response to DNA damage to avoid genomic mutations. Apoptosis of germ cells is closely related to cancer development and chemotherapy resistance; however, its regulatory mechanism is unclear. Here, we suggest that testis-specific lncRNA LINC03074 is involved in male germ cell apoptosis by regulating the expression of the proto-oncogene MDM2. LINC03074 is highly expressed in the sperm of healthy adult testes and cancer cells of testes with testicular germ cell tumors (TGCTs). LINC03074 binds to MDM2 mRNA via an Alu element, thereby reducing MDM2 protein levels. LINC03074 stimulates STAU1-mediated nuclear export of MDM2 mRNA by increasing STAU1 binding to MDM2 mRNA in the cell nucleus, thereby promoting PKR-mediated translational repression in the cytoplasm. The induction of apoptosis in TGCT cells and their responsiveness to the anticancer drug cisplatin is enhanced by LINC03074. Notably, LINC03074 increased E2F1 expression without increasing p53, the primary target of MDM2, and upregulated the apoptotic gene p73, the target gene of E2F1. LINC03074-mediated regulation of apoptosis contributes to the responsiveness of TGCTs to anticancer drug-induced DNA damage.

摘要

生殖细胞在响应DNA损伤时优先诱导凋亡以避免基因组突变。生殖细胞的凋亡与癌症发展和化疗耐药性密切相关;然而,其调控机制尚不清楚。在此,我们表明睾丸特异性长链非编码RNA LINC03074通过调节原癌基因MDM2的表达参与雄性生殖细胞凋亡。LINC03074在健康成年睾丸的精子以及患有睾丸生殖细胞肿瘤(TGCT)的睾丸癌细胞中高表达。LINC03074通过一个Alu元件与MDM2 mRNA结合,从而降低MDM2蛋白水平。LINC03074通过增加STAU1在细胞核中与MDM2 mRNA的结合来刺激STAU1介导的MDM2 mRNA核输出,从而促进细胞质中PKR介导的翻译抑制。LINC03074增强了TGCT细胞中的凋亡诱导及其对抗癌药物顺铂的反应性。值得注意的是,LINC03074增加了E2F1的表达而没有增加MDM2的主要靶标p53,并上调了E2F1的靶基因凋亡基因p73。LINC03074介导的凋亡调控有助于TGCT对抗癌药物诱导的DNA损伤的反应性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f62/11297958/6597357baf81/41420_2024_2119_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f62/11297958/d52aafb743f9/41420_2024_2119_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f62/11297958/7752a0d79295/41420_2024_2119_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f62/11297958/50f8ea285512/41420_2024_2119_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f62/11297958/28124778cf40/41420_2024_2119_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f62/11297958/21c3bc2d84b5/41420_2024_2119_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f62/11297958/6597357baf81/41420_2024_2119_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f62/11297958/d52aafb743f9/41420_2024_2119_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f62/11297958/7752a0d79295/41420_2024_2119_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f62/11297958/50f8ea285512/41420_2024_2119_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f62/11297958/28124778cf40/41420_2024_2119_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f62/11297958/21c3bc2d84b5/41420_2024_2119_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f62/11297958/6597357baf81/41420_2024_2119_Fig6_HTML.jpg

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本文引用的文献

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