Literature DB >> 29324312

The hypoxia-responsive long non-coding RNAs may impact on the tumor biology and subsequent management of breast cancer.

Andrea Kapinova1, Peter Kubatka2, Pavol Zubor3, Olga Golubnitschaja4, Zuzana Dankova5, Sona Uramova6, Ivana Pilchova7, Martin Caprnda8, Radka Opatrilova9, Jan Richnavsky10, Peter Kruzliak11, Jan Danko6.   

Abstract

Long non-coding RNAs (lncRNAs) are DNA transcripts longer than 200 nucleotides without protein-coding potential. As they are key regulators of gene expression at chromatic, transcriptional and posttranscriptional level, they play important role in various biological and pathological processes. Dysregulation of lncRNAs has been observed in several diseases including cancer. Breast cancer is heterogeneous disease with many molecular subtypes specific in different prognosis and treatment responses. Hypoxia, a common micro-environmental feature of rapidly growing tumour is associated with metastases, recurrences and resistance to therapy. Aberrant expression of hypoxia related lncRNAs significantly correlates with poor outcomes in cancer patients, as the lncRNAs play an important regulatory role in the breast cancer-cell survival. Thus, a better understanding of lncRNAs role in the hypoxic conditions of breast cancer is crucial for precise understanding of the tumorigenesis, disease features and poor clinical outcome, especially in highly aggressive breast cancer subtypes (HER2-positive and triple-negative types). Moreover, lncRNAs may represent tumour marker predicting prognosis and therapeutic targets improving precise and personalized therapy for better patient´s survival. In this review, we summarize the recent information on lncRNAs in breast cancer with special focus on the hypoxia-responsive lncRNAs and their potential impact on the prognosis, therapy algorithms and individual outcomes. Presented data helps in better understanding of the specific mechanisms predicting new therapeutic agents and strategies for the pharmacological intervention.
Copyright © 2017 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Breast cancer; Hypoxia-responsive lncRNA; Individual outcomes; Molecular signature; Prediction; Prognosis

Mesh:

Substances:

Year:  2018        PMID: 29324312     DOI: 10.1016/j.biopha.2017.12.104

Source DB:  PubMed          Journal:  Biomed Pharmacother        ISSN: 0753-3322            Impact factor:   6.529


  10 in total

1.  Induction of epithelial-mesenchymal transition (EMT) by hypoxia-induced lncRNA RP11-367G18.1 through regulating the histone 4 lysine 16 acetylation (H4K16Ac) mark.

Authors:  Pei-Hua Peng; Joseph Chieh-Yu Lai; Jeng-Shou Chang; Kai-Wen Hsu; Kou-Juey Wu
Journal:  Am J Cancer Res       Date:  2021-06-15       Impact factor: 6.166

2.  Vandetanib (ZD6474) induces antiangiogenesis through mTOR-HIF-1 alpha-VEGF signaling axis in breast cancer cells.

Authors:  Ling Li; Jingkui Yu; Shuhong Jiao; Wei Wang; Fen Zhang; Shiqing Sun
Journal:  Onco Targets Ther       Date:  2018-11-29       Impact factor: 4.147

Review 3.  LncRNA HOTAIR in Tumor Microenvironment: What Role?

Authors:  Gerardo Botti; Giosuè Scognamiglio; Gabriella Aquino; Giuseppina Liguori; Monica Cantile
Journal:  Int J Mol Sci       Date:  2019-05-08       Impact factor: 5.923

4.  A novel hypoxic long noncoding RNA KB-1980E6.3 maintains breast cancer stem cell stemness via interacting with IGF2BP1 to facilitate c-Myc mRNA stability.

Authors:  Pengpeng Zhu; Fang He; Yixuan Hou; Gang Tu; Qiao Li; Ting Jin; Huan Zeng; Yilu Qin; Xueying Wan; Yina Qiao; Yuxiang Qiu; Yong Teng; Manran Liu
Journal:  Oncogene       Date:  2021-01-19       Impact factor: 9.867

Review 5.  The role of hypoxia-induced long noncoding RNAs (lncRNAs) in tumorigenesis and metastasis.

Authors:  Pei-Hua Peng; Kai-Wen Hsu; Joseph Chieh-Yu Lai; Kou-Juey Wu
Journal:  Biomed J       Date:  2021-03-24       Impact factor: 4.910

Review 6.  RET in breast cancer: pathogenic implications and mechanisms of drug resistance.

Authors:  Cristiana Lo Nigro; Marta Rusmini; Isabella Ceccherini
Journal:  Cancer Drug Resist       Date:  2019-12-19

7.  Hypoxia-induced lncRNA STEAP3-AS1 activates Wnt/β-catenin signaling to promote colorectal cancer progression by preventing m6A-mediated degradation of STEAP3 mRNA.

Authors:  Li Zhou; Jingwen Jiang; Zhao Huang; Ping Jin; Liyuan Peng; Maochao Luo; Zhe Zhang; Yan Chen; Na Xie; Wei Gao; Edouard C Nice; Jing-Quan Li; Hai-Ning Chen; Canhua Huang
Journal:  Mol Cancer       Date:  2022-08-19       Impact factor: 41.444

Review 8.  Conducive target range of breast cancer: Hypoxic tumor microenvironment.

Authors:  Wen Cheng; Xian Xiao; Yang Liao; Qingqing Cao; Chaoran Wang; Xiaojiang Li; Yingjie Jia
Journal:  Front Oncol       Date:  2022-09-26       Impact factor: 5.738

9.  LINC00858 promotes retinoblastoma cell proliferation, migration and invasion by inhibiting miR-3182.

Authors:  Qi Wang; Yanni Zhu; Guojin Zuo; Xiaoming Chen; Jinkui Cheng; Shu Zhang
Journal:  Exp Ther Med       Date:  2019-12-05       Impact factor: 2.447

10.  A positive feedback regulatory loop involving the lncRNA PVT1 and HIF-1α in pancreatic cancer.

Authors:  Yiping Zhu; Fang Wu; Weiwei Gui; Nan Zhang; Erik Matro; Linghua Zhu; Daniel Turunen Eserberg; Xihua Lin
Journal:  J Mol Cell Biol       Date:  2021-12-06       Impact factor: 6.216

  10 in total

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