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11/21/2016 10:43:00 AM | Browse: 633 | Download: 820
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Received |
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2016-06-01 08:30 |
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Peer-Review Started |
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2016-06-09 16:41 |
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2016-07-25 11:53 |
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Return for Revision |
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2016-07-30 15:21 |
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Revised |
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2016-08-08 23:47 |
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Second Decision |
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2016-09-05 09:41 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2016-09-18 14:30 |
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Articles in Press |
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2016-09-18 14:30 |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2016-11-16 12:26 |
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Publish the Manuscript Online |
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2016-11-21 08:10 |
ISSN |
1949-8470 (online) |
Open Access |
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
Copyright |
© The Author(s) 2016. Published by Baishideng Publishing Group Inc. All rights reserved. |
Article Reprints |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
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Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
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Publisher |
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA |
Website |
http://www.wjgnet.com |
Category |
Nuclear Science & Technology |
Manuscript Type |
Minireviews |
Article Title |
Mechanisms underlying 18F-fluorodeoxyglucose accumulation in colorectal cancer
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Manuscript Source |
Invited Manuscript |
All Author List |
Kenji Kawada, Masayoshi Iwamoto and Yoshiharu Sakai |
Funding Agency and Grant Number |
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Corresponding Author |
Kenji Kawada, MD, PhD, Department of Surgery, Graduate School of Medicine, Kyoto University, 54 Shogoin- Kawara-cho, Sakyo-ku, Kyoto 606-8507, Japan. kkawada@kuhp.kyoto-u.ac.jp |
Key Words |
18F-fluorodeoxyglucose-positron emission tomography; Colorectal cancer; Glucose metabolism; Mutational status; KRAS |
Core Tip |
Malignant cancers are preferential to metabolize glucose by glycolysis, even in the presence of oxygen, so-called Warburg effect. This elevated glucose metabolism is responsible for 18F-fluorodeoxyglucose (FDG) accumulation into cancer cells, which results in the positive signals in FDG-positron emission tomography scans. In spite of its clinical utility, the cellular and molecular mechanisms of 18F-FDG accumulation have not yet been elucidated. Here we review the current literature published with respect to the mechanisms of 18F-FDG accumulation into colorectal cancer tissues. |
Publish Date |
2016-11-21 08:10 |
Citation |
Kawada K, Iwamoto M, Sakai Y. Mechanisms underlying 18F-fluorodeoxyglucose accumulation in colorectal cancer. World J Radiol 2016; 8(11): 880-886 |
URL |
http://www.wjgnet.com/1949-8470/full/v8/i11/880.htm |
DOI |
http://dx.doi.org/10.4329/wjr.v8.i11.880 |
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