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MMP-2 和 MMP-9 的蛋白表达,表明 EP-3P 可能是通过                       tion and lipid accumulation of 3T3-L1 adipocytes[J]. Int J
        抑制 MMP-2 和 MMP-9 表达从而影响 MDA-MB-231 细                     Mol Sci,2020,21(2):460.
        胞的迁移和侵袭。                                            [11]  LI H L,WANG H J,WANG J,et al. Design,synthesis and
            综上所述,EP-3P 可通过线粒体介导的内源性 cas-                         biological evaluation of novel 5α,8α-endoperoxide steroi-
        pase途径抑制乳腺癌细胞MDA-MB-231的增殖、迁移和                           dal derivatives with hybrid side chain as anticancer agents
                                                                 [J]. Steroids,2020,153:108471.
        侵袭,并可诱导细胞发生凋亡。本研究结果为后续研究
                                                            [12]  HAN Y L,LIN Y,WANG Y Q,et al. Synthesis and cyto-
        EP-3P 抗乳腺癌作用机制提供了一定参考,但本研究仅
                                                                 toxic evaluation of steroidal endoperoxide derivatives
        采用单一的乳腺癌细胞系进行了实验,有关EP-3P对其
                                                                 with hydrazide side chain as anticancer agents[J]. Hetero-
        他肿瘤细胞及其抗乳腺癌的相关机制有待进一步探
                                                                 cycles,2020,100(5):790-801.
        讨。同时,衍生物EP-3P抑制乳腺癌细胞转移和凋亡的                          [13]  BU M,CAO T T,LI H X,et al. Synthesis of 5α,8α-ergos-
        作用是否优于其先导化合物EP,尚需进一步验证。                                  terol peroxide 3-carbamate derivatives and a fluorescent
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        ·1360 ·  China Pharmacy 2022 Vol. 33 No. 11                                 中国药房    2022年第33卷第11期
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