Genome-wide DNA methylation and RNA expression differences correlate with invasiveness in melanoma cell lines

Author:

Motwani Jyoti1ORCID,Rodger Euan J12ORCID,Stockwell Peter A1,Baguley Bruce C23ORCID,Macaulay Erin C1ORCID,Eccles Michael R12ORCID

Affiliation:

1. Department of Pathology, Otago Medical School – Dunedin Campus, University of Otago, Dunedin 9054, New Zealand

2. Maurice Wilkins Centre for Molecular Biodiscovery, Level 2, 3A Symonds Street, Auckland 1010, New Zealand

3. Auckland Cancer Society Research Centre, The University of Auckland, Auckland 1023, New Zealand

Abstract

Aims & objectives: The aim of this study was to investigate the role of DNA methylation in invasiveness in melanoma cells. Materials & methods: The authors carried out genome-wide transcriptome (RNA sequencing) and reduced representation bisulfite sequencing methylome profiling between noninvasive (n = 4) and invasive melanoma cell lines (n = 5). Results: The integration of differentially expressed genes and differentially methylated fragments (DMFs) identified 12 DMFs (two in AVPI1, one in HMG20B, two in BCL3, one in NTSR1, one in SYNJ2, one in ROBO2 and four in HORMAD2) that overlapped with either differentially expressed genes (eight DMFs and six genes) or cis-targets of lncRNAs (five DMFs associated with cis-targets and four differentially expressed lncRNAs). Conclusions: DNA methylation changes are associated with a number of transcriptional differences observed in noninvasive and invasive phenotypes in melanoma.

Funder

Healthcare Otago Charitable Trust

HS and JC Anderson Trust

Maurice Wilkins Centre for Molecular Biodiscovery

Maurice and Phyllis Paykel Trust

Lottery Health Research NZ

Publisher

Future Medicine Ltd

Subject

Cancer Research,Genetics

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