Alterations in WNT Signaling in Leukemias


Citar

Texto integral

Acesso aberto Acesso aberto
Acesso é fechado Acesso está concedido
Acesso é fechado Somente assinantes

Resumo

The WNT/β–catenin signaling pathway plays an important role in the differentiation and proliferation of hematopoietic cells. In recent years, special attention has been paid to the role of impairments in the WNT signaling path–way in pathogenesis of malignant neoplasms of the hematopoietic system. Disorders in the WNT/β–catenin signaling in leukemias identified to date include hypersensitivity to the WNT ligands, epigenetic repression of WNT antagonists, over–expression of WNT ligands, impaired β–catenin degradation in the cytoplasm, and changes in the activity of the TCF/Lef transcription factors. At the molecular level, these impairments involve overexpression of the FZD protein, hypermethylation of the SFRP, DKK, WiF, Sox, and CXXC gene promoters, overexpression of Lef1 and plakoglobin, mutations in GSK3β, and β–catenin phosphorylation by the BCR–ABL kinase. This review is devoted to the systematization of these data.

Sobre autores

T. Fetisov

Blokhin National Medical Research Center of Oncology

Email: belitsga@mail.ru
Rússia, Moscow, 115478

E. Lesovaya

Blokhin National Medical Research Center of Oncology; Pavlov Ryazan State Medical University

Email: belitsga@mail.ru
Rússia, Moscow, 115478; Ryazan, 390026

M. Yakubovskaya

Blokhin National Medical Research Center of Oncology

Email: belitsga@mail.ru
Rússia, Moscow, 115478

K. Kirsanov

Blokhin National Medical Research Center of Oncology; Peoples’ Friendship University of Russia

Email: belitsga@mail.ru
Rússia, Moscow, 115478; Moscow, 117198

G. Belitsky

Blokhin National Medical Research Center of Oncology

Autor responsável pela correspondência
Email: belitsga@mail.ru
Rússia, Moscow, 115478


Declaração de direitos autorais © Pleiades Publishing, Inc., 2018

Este site utiliza cookies

Ao continuar usando nosso site, você concorda com o procedimento de cookies que mantêm o site funcionando normalmente.

Informação sobre cookies