Superiority of [11C]methionine over [18F]deoxyglucose for PET Imaging of Multiple Cancer Types Due to the Methionine Addiction of Cancer

Author:

Kubota Yutaro123ORCID,Sato Toshihiko4,Hozumi Chihiro5,Han Qinghong1,Aoki Yusuke12,Masaki Noriyuki12,Obara Koya12,Tsunoda Takuya3ORCID,Hoffman Robert M.12

Affiliation:

1. AntiCancer Inc., 7917 Ostrow Str., San Diego, CA 92111-3604, USA

2. Department of Surgery, University of California, San Diego, CA 92037-7220, USA

3. Division of Internal Medicine, Department of Medical Oncology, Showa University School of Medicine, Tokyo 142-8666, Japan

4. Utsunomiya Central Clinic, Tochigi 321-0112, Japan

5. AntiCancer Japan Inc., Chiba 270-1505, Japan

Abstract

Positron emission tomography (PET) is widely used to detect cancers. The usual isotope for PET imaging of cancer is [18F]deoxyglucose. The premise of using [18F]deoxyglucose is that cancers are addicted to glucose (The Warburg effect). However, cancers are more severely addicted to methionine (The Hoffman effect). [11C]methionine PET (MET-PET) has been effectively used for the detection of glioblastoma and other cancers in the brain, and in comparison, MET-PET has been shown to be more sensitive and accurate than [18F]deoxyglucose PET (FDG-PET). However, MET-PET has been limited to cancers in the brain. The present report describes the first applications of MET-PET to cancers of multiple organs, including rectal, bladder, lung, and kidney. The results in each case show that MET-PET is superior to FDG-PET due to the methionine addiction of cancer and suggest that the broad application of MET-PET should be undertaken for cancer detection.

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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