乙酰唑胺
体内
化学
碳酸酐酶
碳酸酐酶抑制剂
癌症研究
因子IX
生物化学
酶
医学
内科学
生物
生物技术
作者
Kunal N. More,Jeong Yong Lee,Dong‐Yeon Kim,Nam-Chul Cho,Ayoung Pyo,Misun Yun,Hyeon Sik Kim,Hangun Kim,Kwangseok Ko,Jeong‐Hoon Park,Dong‐Jo Chang
标识
DOI:10.1016/j.bmcl.2018.01.060
摘要
Carbonic anhydrase IX is overexpressed in many solid tumors including hypoxic tumors and is a potential target for cancer therapy and diagnosis. Reported imaging agents targeting CA-IX are successful mostly in clear cell renal carcinoma as SKRC-52 and no candidate was approved yet in clinical trials for imaging of CA-IX. To validate CA-IX as a valid target for imaging of hypoxic tumor, we designed and synthesized novel [18F]-PET tracer (1) based on acetazolamide which is one of the well-known CA-IX inhibitors and performed imaging study in CA-IX expressing hypoxic tumor model as 4T1 and HT-29 in vivo models other than SKRC-52. [18F]-acetazolamide (1) was found to be insufficient for the specific accumulation in CA-IX expressing tumor. This study might be useful to understand in vivo behavior of acetazolamide PET tracer and can contribute to the development of successful PET imaging agents targeting CA-IX in future. Additional study is needed to understand the mechanism of poor targeting of CA-IX, as if CA-IX is not reliable as a sole target for imaging of CA-IX expressing hypoxic solid tumors.
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