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RNA Activation

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Cover of 'RNA Activation'

Table of Contents

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    Book Overview
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    Chapter 1 Small RNA-Guided Transcriptional Gene Activation (RNAa) in Mammalian Cells
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    Chapter 2 Enhancing Neuronogenesis and Counteracting Neuropathogenic Gene Haploinsufficiencies by RNA Gene Activation
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    Chapter 3 Target-Recognition Mechanism and Specificity of RNA Activation
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    Chapter 4 Promoter-Targeted Small Activating RNAs Alter Nucleosome Positioning
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    Chapter 5 Endogenous miRNAa: miRNA-Mediated Gene Upregulation
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    Chapter 6 miRNA-Mediated RNA Activation in Mammalian Cells
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    Chapter 7 RNAa Induced by TATA Box-Targeting MicroRNAs
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    Chapter 8 miRNA-Mediated RNAa by Targeting Enhancers
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    Chapter 9 Specific Increase of Protein Levels by Enhancing Translation Using Antisense Oligonucleotides Targeting Upstream Open Frames
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    Chapter 10 Repurposing CRISPR System for Transcriptional Activation
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    Chapter 11 RNA-Mediated Gene Activation: Identifying a Candidate RNA for Preclinical Development
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    Chapter 12 Treatment of Pancreatic Cancer by Aptamer Conjugated C/EBPα-saRNA
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    Chapter 13 Treatment of Liver Cancer by C/EBPA saRNA
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    Chapter 14 Enhancing Angiogenesis in Mice by VEGF-Targeting Small Activating RNAs
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    Chapter 15 Suppression of Prostate Cancer Metastasis by DPYSL3-Targeted saRNA
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    Chapter 16 Development of Therapeutic dsP21-322 for Cancer Treatment
Attention for Chapter 16: Development of Therapeutic dsP21-322 for Cancer Treatment
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Chapter title
Development of Therapeutic dsP21-322 for Cancer Treatment
Chapter number 16
Book title
RNA Activation
Published in
Advances in experimental medicine and biology, June 2017
DOI 10.1007/978-981-10-4310-9_16
Pubmed ID
Book ISBNs
978-9-81-104309-3, 978-9-81-104310-9
Authors

Moo Rim Kang, Gongcheng Li, Tiejun Pan, Jin-Chun Xing, Long-Cheng Li

Editors

Long-Cheng Li

Abstract

Small activating RNAs (saRNAs) are a class of artificially designed short duplex RNAs targeted at the promoter of a particular gene to upregulate its expression via a mechanism known as RNA activation (RNAa) and hold great promise for treating a wide variety of diseases including those undruggable by conventional therapies. The therapeutic benefits of saRNAs have been demonstrated in a number of preclinical studies carried out in different disease models including cancer. With many tumor suppressor genes (TSGs) downregulated due to either epigenetic mechanisms or haploinsufficiency resulting from deletion/mutation, cancer is an ideal disease space for saRNA therapeutics which can restore the expression of TSGs via epigenetic reprogramming. The p21(WAF1/CIP) gene is a TSG frequently downregulated in cancer and an saRNA for p21(WAF1/CIP) known as dsP21-322 has been identified to be a sequence-specific p21(WAF1/CIP) activator in a number of cancer types. In this chapter, we review preclinical development of medicinal dsP21-322 for cancer, especially prostate cancer and bladder cancer, and highlight its potential for further clinical development.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 9 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 9 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 2 22%
Student > Doctoral Student 1 11%
Other 1 11%
Student > Ph. D. Student 1 11%
Professor > Associate Professor 1 11%
Other 0 0%
Unknown 3 33%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 3 33%
Pharmacology, Toxicology and Pharmaceutical Science 1 11%
Computer Science 1 11%
Agricultural and Biological Sciences 1 11%
Unknown 3 33%