Pemetrexed-conjugated hyaluronan for the treatment of malignant pleural mesothelioma

被引:9
作者
Amano, Yuki [1 ]
Ohta, Seiichi [2 ]
Sakura, Kazuma L. [3 ,4 ]
Ito, Taichi [1 ,2 ]
机构
[1] Univ Tokyo, Dept Chem Syst Engn, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan
[2] Univ Tokyo, Ctr Dis Biol & Integrat Med, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1130033, Japan
[3] Osaka Univ Hosp, Resp Ctr, Suita, Osaka 5650871, Japan
[4] Osaka Univ, Dept Surg, Suita, Osaka 5650871, Japan
关键词
Anti-tumor; Drug conjugates; Pemetrexed; Malignant pleural mesothelioma; DIHYDROFOLATE REDUCTASES; PERITONEAL DISSEMINATION; MOLECULAR-WEIGHT; FOLIC-ACID; FOLATE; DOXORUBICIN; INHIBITION; CISPLATIN; CYTOTOXICITY; THYMIDYLATE;
D O I
10.1016/j.ejps.2019.105008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Pemetrexed (PMX) is a multi-targeted antifolate drug used for the treatment of malignant pleural mesothelioma (MPM) and non-small cell lung cancer. Hyaluronan (HA) in blood is well known as a disease marker of MPM. We synthesized PMX-conjugated hyaluronan (HA-ADH-PMX) for the first time to develop a novel anticancer chemotherapeutic agent. HAs with different molecular weights (76 and 130 kDa) were first derivatized with adipic dihydrazide (ADH) and then conjugated to PMX. The obtained HA-ADH-PMX retained inhibitory activity against folate metabolism enzymes; thymidylate synthase was inhibited to the same extent as native PMX, whereas the inhibition constant against dihydrofolate reductase was 3.3% for 76 kDa HA-ADH-PMX and 12% for 130 kDa HA-ADH-PMX when compared with that of native PMX. The in vitro cytotoxicity of HA-ADH-PMX from both molecular weights against MPM cell lines was lower than that of native PMX. On the other hand, intrapleural administration of 76 kDa HA-ADH-PMX resulted in a survival rate of MPM model mice comparable to that with native PMX, suggesting the potential for future MPM therapy.
引用
收藏
页数:10
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