Tumor uptake of radiolabeled acetate reflects the expression of cytosolic acetyl-CoA synthetase: implications for the mechanism of acetate PET

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• 作者：Yukie Yoshii ; Atsuo Waki ; Takako Furukawa ; Yasushi Kiyono ; Tetsuya Mori ; Hiroshi Yoshii ; Takashi Kudo ; Hidehiko Okazawa ; Michael J. Welch ; Yasuhisa Fujibayashi
• 关键词：Acetate ; Acetyl-CoA synthetase ; PET ; Hypoxia ; Tumor
• 刊名：Nuclear Medicine and Biology
• 出版年：2009
• 出版时间：October 2009
• 年：2009
• 卷：36
• 期：7
• 页码：771-777
• 全文大小：418 K

文摘

Introduction

[1-¹¹C]Acetate positron emission tomography (PET) is used for myocardial studies. In the myocardium, mitochondrial acetyl-CoA synthetase (ACSS1) mainly contributes to the radiopharmaceutical uptake. [1-¹¹C]Acetate PET is also used for tumor diagnosis; however, the uptake mechanism of radiolabeled acetate in tumors remains unclear. Our previous study reported that cytosolic acetyl-CoA synthetase (ACSS2) was expressed in tumor cells and up-regulated under hypoxia, whereas expression of ACSS1 was negligible regardless of the oxygen conditions. We also indicated that ACSS2 is a bidirectional enzyme that controls acetyl-CoA/acetate metabolism in tumor cells. In this study, to elucidate the basic mechanism of tumor acetate uptake, we focused on ACSS2 and investigated the role of ACSS2 in the uptake of radiolabeled acetate in tumor cells.

Methods

[1-¹⁴C]Acetate uptake and ACSS2 expression were examined in four tumor cell lines under normoxia or hypoxia. An ACSS2 knockdown study was also performed.

Results

[1-¹⁴C]Acetate uptake was increased in the tumor cells under hypoxia. This pattern followed that of ACSS2 expression. The incorporated ¹⁴C was mostly distributed in the lipid-soluble fractions, and this tendency increased under hypoxia. ACSS2 knockdown led to a corresponding reduction in [1-¹⁴C]acetate uptake in all tumor cell lines examined under normoxia and hypoxia.

Conclusions

ACSS2 plays an important role in the uptake of radiolabeled acetate in tumor cells, which is different from that in the myocardium, which mainly involves ACSS1. The uptake of radiolabeled acetate in tumors increased under hypoxia along with up-regulation of ACSS2 expression. This suggests a possible mechanism for acetate PET for tumors.