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Increased levels of β-catenin, LEF-1, and HPA-1 correlate with poor prognosis for acral melanoma with negative BRAF and NRAS mutation in BRAF exons 11 and 15 and NRAS exons 1 and 2.

Abstract
To determine the expression of β-catenin, lymphoid enhancer-binding protein-1 (LEF-1), and heparanase-1 (HPA-1) and to evaluate these proteins' potential prognostic values in malignant acral melanoma without mutations in BRAF exons 11 and 15 and NRAS exons 1 and 2, specimens from 90 patients with wild-type BRAF and NRAS were assessed and analyzed by immunohistochemistry and western blotting. The positive expression of β-catenin, lymphoid enhancer-binding protein-1, and heparanase-1 was observed in 36 (72%), 31 (62%), and 32 (64%) of the detected acral melanomas, respectively. The expression of β-catenin, lymphoid enhancer-binding protein-1, and heparanase-1 was not correlated with gender, age, or diseased body parts (p>0.05), but was significantly positively correlated with the tumor node metastasis (TNM) stage and metastasis (correlation=0.406 and 0.716, 0.397 and 0.582, 0.353 and 0.579; p=0.040 and 0.0001, 0.0040 and 0.0001, 0.0120 and 0.0001, respectively). We also observed that the increased expression of β-catenin, lymphoid enhancer-binding protein-1, and heparanase-1 was significantly correlated with decreased survival and poor prognosis (p=0.001, 0.010, and 0.023, respectively). A multifactorial analysis using Cox's regression model revealed that β-catenin, lymphoid enhancer-binding protein-1, heparanase-1, and the TNM stage were all independent factors in malignant melanoma (risk ratios were 7.294, 5.550, 5.622, and 4.794; p-values were 0.007, 0.018, 0.018, and 0.029, respectively). This study may provide the basis for the use of β-catenin, lymphoid enhancer-binding protein-1, and heparanase-1 as novel targets in the treatment of malignant invasion and metastasis in acral melanoma cancer. The expression of β-catenin, LEF-1, and HPA-1 was assessed and compared in malignant melanoma with that of peritumoral tissue and benign nevus in the patients with negative mutations in BRAF exons 11 and 15 and NRAS exons 1 and 2. The study may provide the basis for β-catenin, LEF-1, and HPA-1 as new targets in the treatment of malignant invasion and metastasis in melanoma cancer.
AuthorsSanxiong Xu, Zuozhang Yang, Jinyu Zhang, Yongxin Jiang, Yongbin Chen, Hongjun Li, Xuefeng Liu, Da Xu, Yanjin Chen, Yihao Yang, Ya Zhang, Dongxu Li, Junfeng Xia
JournalDNA and cell biology (DNA Cell Biol) Vol. 34 Issue 1 Pg. 69-77 (Jan 2015) ISSN: 1557-7430 [Electronic] United States
PMID25343173 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • CTNNB1 protein, human
  • LEF1 protein, human
  • Lymphoid Enhancer-Binding Factor 1
  • Membrane Proteins
  • beta Catenin
  • BRAF protein, human
  • Proto-Oncogene Proteins B-raf
  • heparanase
  • Glucuronidase
  • GTP Phosphohydrolases
  • NRAS protein, human
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • DNA Mutational Analysis
  • Exons
  • Female
  • GTP Phosphohydrolases (genetics)
  • Glucuronidase (metabolism)
  • Humans
  • Kaplan-Meier Estimate
  • Lymphoid Enhancer-Binding Factor 1 (metabolism)
  • Male
  • Melanoma (genetics, metabolism, mortality, pathology)
  • Membrane Proteins (genetics)
  • Middle Aged
  • Mutation
  • Neoplasm Recurrence, Local (genetics, metabolism, mortality)
  • Prognosis
  • Proportional Hazards Models
  • Proto-Oncogene Proteins B-raf (genetics)
  • Risk
  • Skin Neoplasms (genetics, metabolism, mortality, pathology)
  • Young Adult
  • beta Catenin (metabolism)

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