Cordycepin affects growth factor-dependent gene expression

The natural compound cordycepin (3’-deoxyadenosine) causes a reduction in breast cancer cell viability. Microarray analysis showed that growth related genes are down-regulated by cordycepin. Indeed, mTOR, ERK and AMPK signalling was shown to be altered by cordycepin, but the effect was too fast to b...

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Main Author: Lin, Jialiang
Format: Thesis (University of Nottingham only)
Language:English
Published: 2018
Subjects:
Online Access:https://eprints.nottingham.ac.uk/50823/
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author Lin, Jialiang
author_facet Lin, Jialiang
author_sort Lin, Jialiang
building Nottingham Research Data Repository
collection Online Access
description The natural compound cordycepin (3’-deoxyadenosine) causes a reduction in breast cancer cell viability. Microarray analysis showed that growth related genes are down-regulated by cordycepin. Indeed, mTOR, ERK and AMPK signalling was shown to be altered by cordycepin, but the effect was too fast to be mediated by transcriptional changes. It was hypothesised that cordycepin affected signal transduction through translation. However, polysome profiling did not identify clear candidates for the effects of cordycepin on signal transduction but unveiled that cordycepin leads to translation repression on 5’ terminal oligopyrimidine (TOP) mRNAs. As TOP mRNAs are known to be regulated by mTOR signaling, this result consistently suggests mTOR signaling is inhibited by cordycepin treatment. To test if it is possible that cordycepin affects gene expression via signal transduction, we compared its effects to various signal transduction inhibitors and an activator. So far, Pictilisib, a pan-PI3K inhibitor, is the only inhibitor that mimics both the gene expression and signal transduction effects of cordycepin, indicating the PI3K-PDK1-AKT axis is affected by cordycepin. The RNAs upregulated by cordycepin were highly enriched in a group of non-coding RNAs, which are also appeared to induce during serum withdrawal. Knockdown of poly(A) polymerases induced these RNAs, indicating that they probably are degraded by the PABPN1 and poly(A) polymerase dependent nuclear RNA decay pathway. Thus the data suggest that cordycepin affects gene regulation by two distinct pathways, one affecting signal transduction and growth related mRNA expression and another affecting polyadenylation mediated decay of non-coding mRNAs.
first_indexed 2025-11-14T20:18:22Z
format Thesis (University of Nottingham only)
id nottingham-50823
institution University of Nottingham Malaysia Campus
institution_category Local University
language English
last_indexed 2025-11-14T20:18:22Z
publishDate 2018
recordtype eprints
repository_type Digital Repository
spelling nottingham-508232025-02-28T14:03:43Z https://eprints.nottingham.ac.uk/50823/ Cordycepin affects growth factor-dependent gene expression Lin, Jialiang The natural compound cordycepin (3’-deoxyadenosine) causes a reduction in breast cancer cell viability. Microarray analysis showed that growth related genes are down-regulated by cordycepin. Indeed, mTOR, ERK and AMPK signalling was shown to be altered by cordycepin, but the effect was too fast to be mediated by transcriptional changes. It was hypothesised that cordycepin affected signal transduction through translation. However, polysome profiling did not identify clear candidates for the effects of cordycepin on signal transduction but unveiled that cordycepin leads to translation repression on 5’ terminal oligopyrimidine (TOP) mRNAs. As TOP mRNAs are known to be regulated by mTOR signaling, this result consistently suggests mTOR signaling is inhibited by cordycepin treatment. To test if it is possible that cordycepin affects gene expression via signal transduction, we compared its effects to various signal transduction inhibitors and an activator. So far, Pictilisib, a pan-PI3K inhibitor, is the only inhibitor that mimics both the gene expression and signal transduction effects of cordycepin, indicating the PI3K-PDK1-AKT axis is affected by cordycepin. The RNAs upregulated by cordycepin were highly enriched in a group of non-coding RNAs, which are also appeared to induce during serum withdrawal. Knockdown of poly(A) polymerases induced these RNAs, indicating that they probably are degraded by the PABPN1 and poly(A) polymerase dependent nuclear RNA decay pathway. Thus the data suggest that cordycepin affects gene regulation by two distinct pathways, one affecting signal transduction and growth related mRNA expression and another affecting polyadenylation mediated decay of non-coding mRNAs. 2018-07-20 Thesis (University of Nottingham only) NonPeerReviewed application/pdf en arr https://eprints.nottingham.ac.uk/50823/1/Thesis%20assembly%20corrected%20-%20Lin.pdf Lin, Jialiang (2018) Cordycepin affects growth factor-dependent gene expression. PhD thesis, University of Nottingham. Cordycepin polyadenylation poly(A) tail ncRNA signal transduction polysome profiling RNA-Seq growth factor
spellingShingle Cordycepin
polyadenylation
poly(A) tail
ncRNA
signal transduction
polysome profiling
RNA-Seq
growth factor
Lin, Jialiang
Cordycepin affects growth factor-dependent gene expression
title Cordycepin affects growth factor-dependent gene expression
title_full Cordycepin affects growth factor-dependent gene expression
title_fullStr Cordycepin affects growth factor-dependent gene expression
title_full_unstemmed Cordycepin affects growth factor-dependent gene expression
title_short Cordycepin affects growth factor-dependent gene expression
title_sort cordycepin affects growth factor-dependent gene expression
topic Cordycepin
polyadenylation
poly(A) tail
ncRNA
signal transduction
polysome profiling
RNA-Seq
growth factor
url https://eprints.nottingham.ac.uk/50823/