Prognostic role of NRAS isoforms in Chinese melanoma patients.
Adolescent
Adult
Aged
Aged, 80 and over
Asian People
/ genetics
Biomarkers, Tumor
/ genetics
Child
Female
Follow-Up Studies
GTP Phosphohydrolases
/ genetics
Humans
Male
Melanoma
/ genetics
Membrane Proteins
/ genetics
Middle Aged
Mutation
Prognosis
Protein Isoforms
Retrospective Studies
Skin Neoplasms
/ genetics
Survival Rate
Young Adult
Journal
Melanoma research
ISSN: 1473-5636
Titre abrégé: Melanoma Res
Pays: England
ID NLM: 9109623
Informations de publication
Date de publication:
06 2019
06 2019
Historique:
pubmed:
30
11
2018
medline:
12
9
2019
entrez:
30
11
2018
Statut:
ppublish
Résumé
Neuroblastoma rat-sarcoma viral oncogene homolog (NRAS) isoforms are expressed in melanoma tumor tissues, which have been described in Caucasian melanoma. However, the status and the clinical significance of NRAS isoforms in the Asian population have not been investigated on a large scale. We examined the expression levels of NRAS isoforms of 140 melanoma samples using quantitative real-time PCR. Furthermore, the relationship of mRNA expression of NRAS isoforms to clinicopathological characteristics and survival of patients was analyzed. Statistical analysis showed that NRAS isoform 2 expression was correlated with melanoma subtypes (P=0.007), and NRAS isoform 4 expression was correlated with tumor thickness (P=0.031) and clinical stage (P=0.006). The median overall survival for patients with high expression of NRAS isoform 3 was significantly shorter than that for patients with low expression of NRAS isoform 3 (P=0.007). In addition, high expression of NRAS isoform 5 was associated with a worse prognosis (P=0.049 and 0.002 for overall survival and disease-free survival, respectively). Multivariate Cox regression analysis showed that high expression levels of NRAS isoform 3 and isoform 5 were independent poor prognostic factors for patients. Our results indicated that the mRNA expressions of NRAS isoform 3 and isoform 5 may be novel indicators of the prognosis of Chinese melanoma patients.
Identifiants
pubmed: 30489482
doi: 10.1097/CMR.0000000000000557
doi:
Substances chimiques
Biomarkers, Tumor
0
Membrane Proteins
0
Protein Isoforms
0
GTP Phosphohydrolases
EC 3.6.1.-
NRAS protein, human
EC 3.6.1.-
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM