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激素信号转导和乳腺癌中 RNA 代谢的调控。

The regulation of RNA metabolism in hormone signaling and breast cancer.

机构信息

Center for Pharmacogenetics, Department of Pharmaceutical Sciences, University of Pittsburgh, PA, 15261, USA.

Center for Pharmacogenetics, Department of Pharmaceutical Sciences, University of Pittsburgh, PA, 15261, USA; UPMC Hillman Cancer Institute, University of Pittsburgh, Pittsburgh, PA, 15261, USA; Department of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA, 15261, USA.

出版信息

Mol Cell Endocrinol. 2021 Jun 1;529:111221. doi: 10.1016/j.mce.2021.111221. Epub 2021 Mar 10.

DOI:10.1016/j.mce.2021.111221
PMID:33711334
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8262629/
Abstract

As the most frequent women's cancer, breast cancer causes the second most cancer-related death in women worldwide. Majority of the breast cancers are hormone receptor-positive and commonly treated by hormone therapy. Thus, the expression levels of hormone receptors signaling pathways are pivotal in the development and therapy of breast cancer. The expression of hormone receptors signaling pathways is not only regulated at the transcription level but also at the post-transcription level by both proteins and RNAs. In addition to that, the function of hormone receptors can also be regulated by RNAs. In this review, we summarize the roles of RNAs in hormone receptor-positive breast cancer. We introduce how mRNA stability and protein function of genes in hormone receptors signaling pathways are regulated by RNA-binding proteins, miRNAs, and lncRNAs. We believe these proteins and RNAs can be potential therapeutic targets of breast cancer.

摘要

作为最常见的女性癌症,乳腺癌是全球女性癌症相关死亡的第二大原因。大多数乳腺癌是激素受体阳性的,通常采用激素治疗。因此,激素受体信号通路的表达水平对乳腺癌的发生和治疗至关重要。激素受体信号通路的表达不仅受转录水平的调控,还受蛋白质和 RNA 的转录后调控。此外,激素受体的功能也可以受到 RNA 的调控。在这篇综述中,我们总结了 RNA 在激素受体阳性乳腺癌中的作用。我们介绍了 RNA 结合蛋白、miRNA 和 lncRNA 如何调节激素受体信号通路中基因的 mRNA 稳定性和蛋白质功能。我们相信这些蛋白质和 RNA 可以成为乳腺癌潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fe4/8262629/5eda41cc8ab0/nihms-1708859-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fe4/8262629/c9d1006313e0/nihms-1708859-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fe4/8262629/5eda41cc8ab0/nihms-1708859-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fe4/8262629/c9d1006313e0/nihms-1708859-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fe4/8262629/5eda41cc8ab0/nihms-1708859-f0002.jpg

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2
LncRNA LINP1 confers tamoxifen resistance and negatively regulated by ER signaling in breast cancer.长链非编码 RNA LINP1 通过 ER 信号转导赋予乳腺癌对他莫昔芬的耐药性并负调控其表达。
Cell Signal. 2020 Apr;68:109536. doi: 10.1016/j.cellsig.2020.109536. Epub 2020 Jan 10.
3
-Stabilizing Long Noncoding RNA Promotes Hormone-Refractory Breast Cancer Progression.稳定长链非编码 RNA 促进激素难治性乳腺癌进展。
基于生物学先验的全基因组调控动力学神经 ODEs 模型。
Genome Biol. 2024 May 21;25(1):127. doi: 10.1186/s13059-024-03264-0.
4
Hormonal regulation of miRNA during mammary gland development.乳腺发育过程中 miRNA 的激素调控。
Biol Open. 2024 Jun 15;13(6). doi: 10.1242/bio.060308. Epub 2024 Jun 10.
5
Biologically informed NeuralODEs for genome-wide regulatory dynamics.用于全基因组调控动力学的生物信息神经常微分方程
Res Sq. 2023 Mar 14:rs.3.rs-2675584. doi: 10.21203/rs.3.rs-2675584/v1.
6
Identifying Hub Genes Associated with Neoadjuvant Chemotherapy Resistance in Breast Cancer and Potential Drug Repurposing for the Development of Precision Medicine.鉴定与乳腺癌新辅助化疗耐药相关的枢纽基因,并为精准医学的发展寻找药物再利用的潜力。
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7
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4
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5
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6
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7
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9
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Cell Biol Int. 2017 Dec;41(12):1345-1355. doi: 10.1002/cbin.10841. Epub 2017 Sep 5.
10
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