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Deciphering the roles of lncRNAs in breast development and disease.

作者信息

Richard John Lalith Charles, Eichhorn Pieter Johan Adam

机构信息

Cancer Science Institute of Singapore, National University of Singapore, 117599, Singapore.

Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, 117597, Singapore.

出版信息

Oncotarget. 2018 Feb 28;9(28):20179-20212. doi: 10.18632/oncotarget.24591. eCollection 2018 Apr 13.


DOI:10.18632/oncotarget.24591
PMID:29732012
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5929455/
Abstract

Breast cancer is the second leading cause of cancer related deaths in women. It is therefore important to understand the mechanisms underlying breast cancer development as well as raises the need for enhanced, non-invasive strategies for novel prognostic and diagnostic methods. The emergence of long non-coding RNAs (lncRNAs) as potential key players in neoplastic disease has received considerable attention over the past few years. This relatively new class of molecular regulators has been shown from ongoing research to act as critical players for key biological processes. Deregulated expression levels of lncRNAs have been observed in a number of cancers including breast cancer. Furthermore, lncRNAs have been linked to breast cancer initiation, progression, metastases and to limit sensitivity to certain targeted therapeutics. In this review we provide an update on the lncRNAs associated with breast cancer and mammary gland development and illustrate the versatility of such lncRNAs in gene control, differentiation and development both in normal physiological conditions and in diseased states. We also highlight the therapeutic and diagnostic potential of lncRNAs in cancer.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/082e/5929455/62b419b74972/oncotarget-09-20179-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/082e/5929455/f5ec68c11b4f/oncotarget-09-20179-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/082e/5929455/78cf249312fa/oncotarget-09-20179-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/082e/5929455/2ba48e8b6153/oncotarget-09-20179-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/082e/5929455/12be0d73844e/oncotarget-09-20179-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/082e/5929455/62b419b74972/oncotarget-09-20179-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/082e/5929455/f5ec68c11b4f/oncotarget-09-20179-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/082e/5929455/78cf249312fa/oncotarget-09-20179-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/082e/5929455/2ba48e8b6153/oncotarget-09-20179-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/082e/5929455/12be0d73844e/oncotarget-09-20179-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/082e/5929455/62b419b74972/oncotarget-09-20179-g005.jpg

相似文献

[1]
Deciphering the roles of lncRNAs in breast development and disease.

Oncotarget. 2018-2-28

[2]
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[3]
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[5]
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[6]
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[7]
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[10]
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Epigenomics. 2024

[2]
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Cancers (Basel). 2024-9-23

[3]
The role of lncRNA NEAT1 in human cancer chemoresistance.

Cancer Cell Int. 2024-7-5

[4]
Non-coding RNA regulates the immune microenvironment in recurrent spontaneous abortion (RSA): new insights into immune mechanisms†.

Biol Reprod. 2024-2-10

[5]
Noncoding RNAs in atherosclerosis: regulation and therapeutic potential.

Mol Cell Biochem. 2024-5

[6]
Underexplored reciprocity between genome-wide methylation status and long non-coding RNA expression reflected in breast cancer research: potential impacts for the disease management in the framework of 3P medicine.

EPMA J. 2023-5-22

[7]
LncRNA LINC00205 stimulates osteoporosis and contributes to spinal fracture through the regulation of the miR-26b-5p/KMT2C axis.

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[8]
The Role of Placental Non-Coding RNAs in Adverse Pregnancy Outcomes.

Int J Mol Sci. 2023-3-6

[9]
Recent Clinical Advances on Long Non-Coding RNAs in Triple-Negative Breast Cancer.

Cells. 2023-2-20

[10]
Underexpression of in -Positive Cases Is Associated With Poor Prognosis in Children With B-Cell Precursor Acute Lymphoblastic Leukemia.

Front Oncol. 2022-6-2

本文引用的文献

[1]
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J Clin Invest. 2017-9-1

[2]
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Long Noncoding RNAs CUPID1 and CUPID2 Mediate Breast Cancer Risk at 11q13 by Modulating the Response to DNA Damage.

Am J Hum Genet. 2017-8-3

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Targeting long non-coding RNA DANCR inhibits triple negative breast cancer progression.

Biol Open. 2017-9-15

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Circular RNA circ-ABCB10 promotes breast cancer proliferation and progression through sponging miR-1271.

Am J Cancer Res. 2017-7-1

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Inhibition of long non-coding RNA ROR reverses resistance to Tamoxifen by inducing autophagy in breast cancer.

Tumour Biol. 2017-6

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Identification and characterization of long intergenic noncoding RNAs in bovine mammary glands.

BMC Genomics. 2017-6-19

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Targeting long non-coding RNA ASBEL with oligonucleotide antagonist for breast cancer therapy.

Biochem Biophys Res Commun. 2017-8-5

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Oncogene. 2017-8-24

[10]
lncRNA NEAT1 is closely related with progression of breast cancer via promoting proliferation and EMT.

Eur Rev Med Pharmacol Sci. 2017-3

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