Can Wnt5a and Wnt non-canonical pathways really mediate adipocyte de-differentiation in a tumour microenvironment?

被引:23
作者
Chirumbolo, Salvatore [1 ]
Bjorklund, Geir [2 ]
机构
[1] Univ Verona, Dept Med, Verona, Italy
[2] Council Nutr & Environm Med, Mo I Rana, Norway
关键词
Cancer; Pancreas; Wnt5a; Beta-catenin pathway; De-dedifferentiation; Adipocyte; MESENCHYMAL STEM-CELLS; TOLL-LIKE RECEPTOR-3; PANCREATIC-CANCER; BETA-ESTRADIOL; UP-REGULATION; MCF-7; CELLS; PPAR-GAMMA; ADIPOGENESIS; EXPRESSION; PHENYLMETHIMAZOLE;
D O I
10.1016/j.ejca.2016.05.026
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Wnt5a has been recently reported as a possible triggering factor of adipocyte dedifferentiation into an adipocyte-derived fibroblast in the tumour microenvironment of pancreas cancer. The Wnt/beta-catenin pathway was described in processes involving dedifferentiation and epithelial-mesenchymal transition but some Wnt family-belonging molecules exert an adipogenic role on adipocyte, while other ones, such as Wnt10b or Wnt3a, an anti-adipogenic role. Although this ability depends on the different tumoural microenvironments, it is intriguing to ascertain if some Wnt molecules, participating in the non-canonical pathway, may be targeted as fundamental factors able to trigger the desmoplastic reaction of peritumoural white adipose tissue. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:96 / 100
页数:5
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