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(4R)-(-)-2-硫代-4-噻唑烷羧酸和 3-巯基丙酸铜配合物通过荧光显微镜成像对前列腺癌和乳腺癌细胞的抗癌活性。

Anticancer Activity of Copper Complex of (4R)-(-)-2-Thioxo-4-thiazolidinecarboxylic Acid and 3-Rhodaninepropionic Acid on Prostate and Breast Cancer Cells by Fluorescent Microscopic Imaging.

机构信息

Department of Radiology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX, 75390-8542, USA.

Advanced Imaging Research Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.

出版信息

J Fluoresc. 2018 Jan;28(1):89-96. doi: 10.1007/s10895-017-2177-0. Epub 2017 Sep 9.

Abstract

Copper complexes with strong anticancer activity are promising new drugs for treatment of patients with metastatic cancer. Copper 8-hydroxyquinoline-2-carboxaldehyde-thiosemicarbazide (CuHQTS) and copper 8-hydroxyquinoline-2-carboxaldehyde-4,4-dimethyl-3-thiosemicarbazide (CuHQDMTS) were found to have strong anticancer activity against cisplatin-resistant neuroblastoma cells and prostate cancer cells. This study aimed to synthesize and characterize two new anticancer copper complexes, copper complex of (4R)-(-)-2-Thioxo-4-thiazolidinecarboxylic acid (CuTTDC), and copper complex of 3-Rhodaninepropionic acid-copper complex (CuRDPA). Cell growth inhibition and cytotoxicity of CuTTDC and CuRDPA on prostate and breast cancer cells were evaluated with Cell Counting Kits-8 (CCK8) assay and fluorescent microscopic imaging respectively. Strong anticancer activity of CuTTDC and CuRDPA was demonstrated by growth inhibition and cytotoxicity of prostate and breast cancer cells treated with these two copper complexes, supporting further investigation of potential use of these two new anticancer complexes for treatment of prostate and breast cancer metastasis.

摘要

具有强抗癌活性的铜配合物是治疗转移性癌症患者的有前途的新药。铜 8-羟基喹啉-2-醛-硫代半卡巴腙(CuHQTS)和铜 8-羟基喹啉-2-醛-4,4-二甲基-3-硫代半卡巴腙(CuHQDMTS)被发现对顺铂耐药神经母细胞瘤细胞和前列腺癌细胞具有强抗癌活性。本研究旨在合成和表征两种新的抗癌铜配合物,(4R)-(-)-2-硫代-4-噻唑烷羧酸铜(CuTTDC)和 3-巯基丙磺酸-铜配合物(CuRDPA)。用细胞计数试剂盒-8(CCK8)测定法评估了 CuTTDC 和 CuRDPA 对前列腺癌和乳腺癌细胞的细胞生长抑制和细胞毒性,并用荧光显微镜成像分别评估了 CuTTDC 和 CuRDPA 对前列腺癌和乳腺癌细胞的细胞毒性。CuTTDC 和 CuRDPA 对前列腺癌和乳腺癌细胞的生长抑制和细胞毒性表明其具有很强的抗癌活性,支持进一步研究这两种新型抗癌配合物在治疗前列腺癌和乳腺癌转移中的潜在用途。

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