Literature DB >> 26300548

The functional relevance of somatic synonymous mutations in melanoma and other cancers.

Valer Gotea1, Jared J Gartner2, Nouar Qutob3, Laura Elnitski1, Yardena Samuels3.   

Abstract

Recent technological advances in sequencing have flooded the field of cancer research with knowledge about somatic mutations for many different cancer types. Most cancer genomics studies focus on mutations that alter the amino acid sequence, ignoring the potential impact of synonymous mutations. However, accumulating experimental evidence has demonstrated clear consequences for gene function, leading to a widespread recognition of the functional role of synonymous mutations and their causal connection to various diseases. Here, we review the evidence supporting the direct impact of synonymous mutations on gene function via gene splicing; mRNA stability, folding, and translation; protein folding; and miRNA-based regulation of expression. These results highlight the functional contribution of synonymous mutations to oncogenesis and the need to further investigate their detection and prioritization for experimental assessment.
© 2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  cancer; gene splicing; melanoma; miRNA regulation; protein folding; protein translation; secondary structure; synonymous mutations

Mesh:

Year:  2015        PMID: 26300548      PMCID: PMC4834044          DOI: 10.1111/pcmr.12413

Source DB:  PubMed          Journal:  Pigment Cell Melanoma Res        ISSN: 1755-1471            Impact factor:   4.693


  138 in total

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3.  Inference of mutation parameters and selective constraint in mammalian coding sequences by approximate Bayesian computation.

Authors:  Peter D Keightley; Lél Eöry; Daniel L Halligan; Mark Kirkpatrick
Journal:  Genetics       Date:  2011-02-01       Impact factor: 4.562

Review 4.  Decoding mechanisms by which silent codon changes influence protein biogenesis and function.

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5.  Different mutation profiles associated to P53 accumulation in colorectal cancer.

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6.  Synonymous mutations frequently act as driver mutations in human cancers.

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7.  Cancer and genomics.

Authors:  P A Futreal; A Kasprzyk; E Birney; J C Mullikin; R Wooster; M R Stratton
Journal:  Nature       Date:  2001-02-15       Impact factor: 49.962

Review 8.  The molecular genetics of cellular oncogenes.

Authors:  H E Varmus
Journal:  Annu Rev Genet       Date:  1984       Impact factor: 16.830

9.  A comprehensive catalogue of somatic mutations from a human cancer genome.

Authors:  Erin D Pleasance; R Keira Cheetham; Philip J Stephens; David J McBride; Sean J Humphray; Chris D Greenman; Ignacio Varela; Meng-Lay Lin; Gonzalo R Ordóñez; Graham R Bignell; Kai Ye; Julie Alipaz; Markus J Bauer; David Beare; Adam Butler; Richard J Carter; Lina Chen; Anthony J Cox; Sarah Edkins; Paula I Kokko-Gonzales; Niall A Gormley; Russell J Grocock; Christian D Haudenschild; Matthew M Hims; Terena James; Mingming Jia; Zoya Kingsbury; Catherine Leroy; John Marshall; Andrew Menzies; Laura J Mudie; Zemin Ning; Tom Royce; Ole B Schulz-Trieglaff; Anastassia Spiridou; Lucy A Stebbings; Lukasz Szajkowski; Jon Teague; David Williamson; Lynda Chin; Mark T Ross; Peter J Campbell; David R Bentley; P Andrew Futreal; Michael R Stratton
Journal:  Nature       Date:  2009-12-16       Impact factor: 49.962

10.  Mutation and cancer: statistical study of retinoblastoma.

Authors:  A G Knudson
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  25 in total

1.  Synonymous variants that disrupt messenger RNA structure are significantly constrained in the human population.

Authors:  Jeffrey B S Gaither; Grant E Lammi; James L Li; David M Gordon; Harkness C Kuck; Benjamin J Kelly; James R Fitch; Peter White
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Review 3.  Genomic sequencing and precision medicine in head and neck cancers.

Authors:  R C Hoesli; M L Ludwig; N L Michmerhuizen; A J Rosko; M E Spector; J C Brenner; A C Birkeland
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Review 4.  Synonymous Variants: Necessary Nuance in Our Understanding of Cancer Drivers and Treatment Outcomes.

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5.  A Schizophrenia-Linked KALRN Coding Variant Alters Neuron Morphology, Protein Function, and Transcript Stability.

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6.  Variation in a Newly Identified Caprine KRTAP Gene Is Associated with Raw Cashmere Fiber Weight in Longdong Cashmere Goats.

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7.  A highly polymorphic caprine keratin-associated protein gene identified and its effect on cashmere traits.

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8.  A Case of IL-7R Deficiency Caused by a Novel Synonymous Mutation and Implications for Mutation Screening in SCID Diagnosis.

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9.  Variation in the Ovine KAP6-3 Gene (KRTAP6-3) Is Associated with Variation in Mean Fibre Diameter-Associated Wool Traits.

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10.  Systems analysis identifies melanoma-enriched pro-oncogenic networks controlled by the RNA binding protein CELF1.

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Journal:  Nat Commun       Date:  2017-12-21       Impact factor: 14.919

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