Abstract

Metastasis is the major cause of cancer-related death in breast cancer patients, which is controlled by specific sets of genes. Targeting these genes may provide a means to delay cancer progression and allow local treatment to be more effective. We report for the first time that ADP-ribosylation factor 1 (ARF1) is the most amplified gene in ARF gene family in breast cancer, and high-level amplification of ARF1 is associated with increased mRNA expression and poor outcomes of patients with breast cancer. Knockdown of ARF1 leads to significant suppression of migration and invasion in breast cancer cells. Using the orthotopic xenograft model in NSG mice, we demonstrate that loss of ARF1 expression in breast cancer cells inhibits pulmonary metastasis. The zebrafish-metastasis model confirms that the ARF1 gene depletion suppresses breast cancer cells to metastatic disseminate throughout fish body, indicating that ARF1 is a very compelling target to limit metastasis. ARF1 function largely dependents on its activation and LM11, a cell-active inhibitor that specifically inhibits ARF1 activation through targeting the ARF1-GDP/ARNO complex at the Golgi, significantly impairs metastatic capability of breast cancer cell in zebrafish. These findings underline the importance of ARF1 in promoting metastasis and suggest that LM11 that inhibits ARF1 activation may represent a potential therapeutic approach to prevent or treat breast cancer metastasis.

Highlights

  • Death due to breast cancer results largely from metastatic spread of the disease [1, 2]

  • Functional plotting of the corresponding mRNA level in relation to genetic status of ADP-ribosylation factor 1 (ARF1) revealed that amplification of ARF1 was associated with increased mRNA expression (Figure 1B)

  • To further validate these findings, the relative expression of the ARF1 transcript was examined in breast cancer entities from the Oncomine database, which showed ARF1 expression levels were significantly higher in cancer than normal tissues (Figure 1C)

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Summary

Introduction

Death due to breast cancer results largely from metastatic spread of the disease [1, 2]. This process encourages cells to break apart from the tumor and travel through the body to another organ [2, 3]. ARF1 and ARF6 are well characterized as crucial regulators for vesicular trafficking, and their roles have been implicated in the cancer progression. Unlike ARF6, ARF1 especially regulates translocation of proteins from trans-Golgi network to plasma membrane, and directly activates signaling molecules [7, 14,15,16]

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