Oncotarget

Research Papers:

Sulfonamide derivative targeting carbonic anhydrase IX as a nuclear imaging probe for colorectal cancer detection in vivo

Siao-Syun Guan _, Chun-Chia Cheng, Ai-Sheng Ho, Chia-Chi Wang, Tsai-Yueh Luo, Tse-Zung Liao, Jungshan Chang, Cheng-Tien Wu and Shing-Hwa Liu

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Oncotarget. 2015; 6:36139-36155. https://doi.org/10.18632/oncotarget.5684

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Abstract

Siao-Syun Guan1,2, Chun-Chia Cheng1,3, Ai-Sheng Ho4, Chia-Chi Wang5, Tsai-Yueh Luo1, Tse-Zung Liao1, Jungshan Chang3, Cheng-Tien Wu2, Shing-Hwa Liu2,6,7

1Institute of Nuclear Energy Research, Atomic Energy Council, Taoyuan, Taiwan

2Institute of Toxicology, College of Medicine, National Taiwan University, Taipei, Taiwan

3Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan

4Division of Gastroenterology, Cheng Hsin General Hospital, Taipei, Taiwan

5Division of Hepatology, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation and School of Medicine, Tzu Chi University, Hualien, Taiwan

6Department of Medical Research, China Medical University Hospital, China Medical University, Taichung, Taiwan

7Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan

Correspondence to:

Shing-Hwa Liu, e-mail: shinghwaliu@ntu.edu.tw

Keywords: colorectal cancer, carbonic anhydrase IX, sulfonamide, radioisotope-labeled

Received: June 26, 2015     Accepted: September 21, 2015     Published: October 05, 2015

ABSTRACT

Hypoxic microenvironment is a common situation in solid tumors. Carbonic anhydrase IX (CA9) is one of the reliable cellular biomarkers of hypoxia. The role of CA9 in colorectal cancer (CRC) remains to be clarified. CA9 inhibitor such as sulfonamides is known to block CA9 activation and reduce tumor growth consequently. Here, we aimed to investigate the CA9 expression in serum and tumor from different stages of CRC patients and utilize sulfonamide derivative with indium-111 labeling as a probe for CRC nuclear imaging detection in vivo. The serum CA9 was correlated with the tumor CA9 levels in different stages of CRC patients. Hypoxia increased cell viability and CA9 expression in colorectal cancer HCT-15 cells. Sulfonamide derivative 5-(2-aminoethyl)thiophene-2-sulfonamide (ATS) could bind with CA9 in vitro under hypoxia. Moreover, tumor tissues in HCT-15-induced xenograft mice possessed higher hypoxic fluorescence signal as compared with other organs. We also found that the radioisotope signal of indium-111 labeled ATS, which was utilized for CRC detection in HCT-15-induced xenograft mice, was markedly enhanced in tumors as compared with non-ATS control. Taken together, these findings suggest that CA9 is a potential hypoxic CRC biomarker and measurement of serum CA9 can be as a potential tool for diagnosing CA9 expressions in CRC clinical practice. The radioisotope-labeled sulfonamide derivative (ATS) may be useful to apply in CRC patients for nuclear medicine imaging.


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