Abstract

Renal cell carcinoma (RCC) encompasses various tumor types characterized by a variety of genetic abnormalities. The genetic changes, like mutations, deletions, and epigenetic alterations, can affect the signaling components and signaling networks, causing the modification of tumor pathogenesis and prognosis of RCC. The most prevalent RCC, clear cell RCC (ccRCC), is asymptomatic in the early stages, refractory to chemotherapy and radiation therapy, and has a poorer prognosis compared with the papillary and chromophobe ccRCC types. Loss of the VHL gene and upregulation of oxygen sensors, hypoxiainducible factor alphas (HIF-α), which promote different growth factors, is a signature of sporadic ccRCC. The VHL-HIF-α and Wnt/β-catenin pathways are closely connected and contribute to the ontogeny of ccRCC. This review confines to ccRCC and the role of the Wnt/β-catenin signaling pathways and its crosstalk with VHL/HIF.

Highlights

  • Renal cell carcinoma (RCC) is composed of a heterogeneous group of tumors originating from different parts of the nephron, maintaining distinct genetic and histological characteristics, which is more prevalent in men (5%) than in women (3%) worldwide [1]

  • The non-commonly occurring RCC types are clear cell (ccRCC) types show the aberrations of discrete genes and signaling pathways and display a hypovascular feature [4, 5]

  • The most common genetic aberrations encountered in ccRCCs are loss chromosome 3p25, leading to the inactivation of the von Hippel–Lindau (VHL) gene [6]

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Summary

Introduction

Renal cell carcinoma (RCC) is composed of a heterogeneous group of tumors originating from different parts of the nephron, maintaining distinct genetic and histological characteristics, which is more prevalent in men (5%) than in women (3%) worldwide [1]. This review confines to ccRCC and the role of the Wnt/β-catenin signaling pathways and its crosstalk with VHL/HIF. In ccRCC, VHL regulates the cellular oxygen sensing mechanism but is involved in Wnt/β-catenin mediated signaling pathways [13, 14].

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