Abstract
Cutaneous melanoma (CM) is the most lethal form of skin cancers. The Hippo pathway controls cell migration, development and sizes of the organs in diverse species, and deregulation of this pathway may affect CM progression and prognosis. Therefore, we hypothesized that genetic variants of Hippo pathway genes might predict survival of CM patients. We used the genotyping data of 1,115 common single nucleotide polymorphisms (SNPs) in the 12 pathway core genes (i.e., MST1, MST2, SAV1, LATS1, LATS2, MOB1A, MOB1B, YAP1, TEAD1, TEAD2, TEAD3 and TEAD4) from the dataset of our previously published CM genome-wide association study and comprehensively analyzed their associations with CM-specific survival (CSS) in 858 CM patients by using the Kaplan-Meier analyses and Cox proportional hazards regression models. We found a predictive role of YAP1 rs11225163 CC, TEAD1 rs7944031 AG+GG and TEAD4 rs1990330 CA+AA in the prognosis of CM. In addition, patients with an increasing number of unfavorable genotypes (NUG) had a markedly increased risk of death. After incorporating NUG in the model with clinical variables, the new model showed a significantly improved discriminatory ability to classify CSS (AUC increased from 82.03% to 84.56%). Our findings suggest that genetic variants of Hippo pathway genes, particularly YAP1 rs11225163, TEAD1 rs7944031 and TEAD4 rs1990330, may independently or jointly modulate survival of CM patients. Additional large, prospective studies are needed to validate these findings.
Keywords
Cox regression
Hippo pathway
cancer specific survival
cutaneous melanoma
single nucleotide polymorphisms
MeSH 主题词
Adaptor Proteins, Signal Transducing/genetics
Adolescent
Adult
Aged
Aged, 80 and over
Alleles
Case-Control Studies
DNA Methylation
DNA-Binding Proteins/genetics
Female
Gene Expression
Genetic Variation
Genotype
Hippo Signaling Pathway
Humans
Male
Melanoma/genetics,metabolism,mortality,pathology
Middle Aged
Muscle Proteins/genetics
Neoplasm Staging
Nuclear Proteins/genetics
Phosphoproteins/genetics
Polymorphism, Single Nucleotide
Prognosis
Protein Serine-Threonine Kinases/metabolism
ROC Curve
Signal Transduction
TEA Domain Transcription Factors
Transcription Factors/genetics
YAP-Signaling Proteins
Young Adult
化学物质
Adaptor Proteins, Signal Transducing
DNA-Binding Proteins
Muscle Proteins
Nuclear Proteins
Phosphoproteins
TEA Domain Transcription Factors
TEAD1 protein, human
TEAD4 protein, human
Transcription Factors
YAP-Signaling Proteins
YAP1 protein, human
Protein Serine-Threonine Kinases
作者与单位
共 8 位作者,点击展开单位 / ORCID
Yuan Hua
Duke Cancer Institute, Duke University Medical Center, Durham, NC. | Department of Medicine, Duke University School of Medicine, Durham, NC. | Department of Oral and Maxillofacial Surgery, Affiliated Hospital of Stomatology, Nanjing Medical University, Nanjing, China.
Liu Hongliang
Duke Cancer Institute, Duke University Medical Center, Durham, NC. | Department of Medicine, Duke University School of Medicine, Durham, NC.
Liu Zhensheng
Duke Cancer Institute, Duke University Medical Center, Durham, NC. | Department of Medicine, Duke University School of Medicine, Durham, NC.
Zhu Dakai
Community and Family Medicine, Geisel School of Medicine, Dartmouth College, Hanover, NH.
Amos Christopher I
Community and Family Medicine, Geisel School of Medicine, Dartmouth College, Hanover, NH.
Fang Shenying
Department of Surgical Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, TX.
Lee Jeffrey E
Department of Surgical Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, TX.
Wei Qingyi
Duke Cancer Institute, Duke University Medical Center, Durham, NC. | Department of Medicine, Duke University School of Medicine, Durham, NC.