Development of a Dichloroacetic Acid-Hemoglobin Conjugate as a Potential Targeted Anti-Cancer Therapeutic

被引:30
|
作者
Zhang, Ning [2 ]
Palmer, Andre F. [1 ]
机构
[1] 231A Koffolt Labs, Columbus, OH 43210 USA
[2] Ohio State Univ, William G Lowrie Dept Chem & Biomol Engn, Columbus, OH 43210 USA
关键词
dichloroacetic acid; hemoglobin; targeted drug delivery; macrophage; monocyte; CD-163; receptor; CANCER-CELLS; APOPTOSIS; IDENTIFICATION; MELAS;
D O I
10.1002/bit.23071
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This work focuses on conjugating the anticancer drug dichloroacetic acid (DCA) to the monocyte/macrophage targeting protein hemoglobin (Hb). The DCA-Hb conjugate carries approximately 12 DCA molecules per Hb tetramer, and binds to haptoglobin (Hp) forming stable DCA-Hb-Hp complexes, in a similar manner to unmodified Hb. The results of this study show that DCA-Hb-Hp is taken up by the monocytic cancer cell line THP-1, where it depolarizes the mitochondrial membrane potential, thereby inhibiting cancerous cell growth at a comparable level to free DCA. Taken together, the results of this study show promise for the use of the DCA-Hb conjugate as a potential therapeutic to treat monocytic leukemia. Biotechnol. Bioeng. 2011; 108: 1413-1420. (C) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:1413 / 1420
页数:8
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