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长应激诱导非编码转录本5:癌症治疗中一个有前景的治疗靶点。

Long stress-induced non-coding transcript 5: A promising therapeutic target for cancer treatment.

作者信息

Yang Wei, Yang Xiaoyan, Li Qing, Cao Pu, Tang Liyang, Xie Zhizhong, Lei Xiaoyong

机构信息

Institute of Pharmacy and Pharmacology, School of Pharmacy, University of South China, Hengyang, China.

The Hunan Provincial Key Laboratory of Tumor Microenvironment Responsive Drug Research, University of South China, Hengyang, China.

出版信息

Adv Clin Exp Med. 2023 Jan;32(1):97-106. doi: 10.17219/acem/152705.

DOI:10.17219/acem/152705
PMID:36083254
Abstract

Long non-coding RNAs are RNA molecules with a transcript length of more than 200 nucleotides and without protein-coding ability. They regulate gene expression by interacting with protein, RNA and DNA. Their function is closely related to their subcellular localization, with regulation of gene expression at the epigenetic and transcriptional levels occurring in the nucleus, and at the post-transcriptional and translational levels in the cytoplasm. Long stress-induced non-coding transcript 5 (LSINCT5), which is localized in the nucleus, is overexpressed in many types of cancers such as breast cancer, gastric cancer, ovarian cancer, thyroid cancer, and gastrointestinal cancer. Substantial evidence indicates that there is an obvious connection between cancers and LSINCT5, as it inhibits apoptosis and promotes proliferation, invasion and migration of cancer cells, as well as participates in the pathogenesis and progression of cancer by interacting with DNA, protein and RNA. These findings suggest that LSINCT5 could be a novel biomarker and an emerging therapeutic target in human cancers. In the present study, the structure and corresponding biological function of LSINCT5 were summarized in order to clarify its molecular mechanisms in the progression of various malignant tumors.

摘要

长链非编码RNA是一类转录本长度超过200个核苷酸且无蛋白质编码能力的RNA分子。它们通过与蛋白质、RNA和DNA相互作用来调节基因表达。其功能与其亚细胞定位密切相关,在细胞核中发生表观遗传和转录水平的基因表达调控,在细胞质中发生转录后和翻译水平的调控。定位于细胞核的长应激诱导非编码转录本5(LSINCT5)在多种癌症中过度表达,如乳腺癌、胃癌、卵巢癌、甲状腺癌和胃肠道癌。大量证据表明癌症与LSINCT5之间存在明显关联,因为它抑制细胞凋亡,促进癌细胞的增殖、侵袭和迁移,并通过与DNA、蛋白质和RNA相互作用参与癌症的发病机制和进展。这些发现表明LSINCT5可能是人类癌症中的一种新型生物标志物和新兴治疗靶点。在本研究中,总结了LSINCT5的结构和相应生物学功能,以阐明其在各种恶性肿瘤进展中的分子机制。

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Long stress-induced non-coding transcript 5: A promising therapeutic target for cancer treatment.长应激诱导非编码转录本5:癌症治疗中一个有前景的治疗靶点。
Adv Clin Exp Med. 2023 Jan;32(1):97-106. doi: 10.17219/acem/152705.
2
LSINCT5: A Novel lncRNA in Cancers.LSINCT5:癌症中的一种新长链非编码 RNA。
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Long non-coding RNA LSINCT5 predicts negative prognosis and exhibits oncogenic activity in gastric cancer.长链非编码RNA LSINCT5预测胃癌预后不良并具有致癌活性。
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The long non-coding RNA LSINCT5 promotes malignancy in non-small cell lung cancer by stabilizing HMGA2.长非编码 RNA LSINCT5 通过稳定 HMGA2 促进非小细胞肺癌的恶性转化。
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Long Stress Induced Non-Coding Transcripts 5 (LSINCT5) Promotes Hepatocellular Carcinoma Progression Through Interaction with High-Mobility Group AT-hook 2 and MiR-4516.长应激诱导非编码转录本 5(LSINCT5)通过与高迁移率族 AT 钩 2 和 miR-4516 相互作用促进肝癌进展。
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LSINCT5 is over expressed in breast and ovarian cancer and affects cellular proliferation.LSINCT5 在乳腺癌和卵巢癌中过表达,并影响细胞增殖。
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Effect of long noncoding RNA long stressinduced noncoding transcript 5 on erlotinib resistance to lung cancer cells and the underlying mechanisms.长链非编码RNA长应激诱导非编码转录本5对肺癌细胞厄洛替尼耐药性的影响及其潜在机制
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LSINCT5 activates Wnt/β-catenin signaling by interacting with NCYM to promote bladder cancer progression.LSINCT5 通过与 NCYM 相互作用激活 Wnt/β-catenin 信号通路,促进膀胱癌的进展。
Biochem Biophys Res Commun. 2018 Jul 20;502(3):299-306. doi: 10.1016/j.bbrc.2018.05.076. Epub 2018 May 30.

引用本文的文献

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Female and male hormonal-dependent malignancies: the role of long non-coding RNAs.女性和男性激素依赖性恶性肿瘤:长链非编码RNA的作用
Med Oncol. 2025 Aug 24;42(10):444. doi: 10.1007/s12032-025-03001-y.
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LncRNA TCL6 regulates miR-876-5p/MYL2 axis to suppress breast cancer progression.长链非编码RNA TCL6通过调控miR-876-5p/MYL2轴抑制乳腺癌进展。
Transl Oncol. 2025 Mar;53:102210. doi: 10.1016/j.tranon.2024.102210. Epub 2025 Jan 27.
3
lncRNA IGF2-AS regulates miR-500a-3p/PPP4R1/p-VEGFR2 signalling pathway to promote thyroid carcinoma progression and tubulogenesis.
长链非编码RNA IGF2-AS通过调控miR-500a-3p/PPP4R1/p-VEGFR2信号通路促进甲状腺癌进展及血管生成。
Clin Transl Med. 2023 Apr;13(4):e1240. doi: 10.1002/ctm2.1240.