中文   |   English   |   Email Alert

磷光环金属化铱(Ⅲ)配合物在癌症治疗方面的应用

何良1, 谭彩萍1, 曹乾1, 毛宗万1,2*

化学进展 ›› 2018, Vol. 30 ›› Issue (10) :1548-1556

PDF (1629KB)
化学进展 ›› 2018, Vol. 30 ›› Issue (10) :1548-1556 DOI: 10.7536/PC180610
综述
扫码查看或转发全文

磷光环金属化铱(Ⅲ)配合物在癌症治疗方面的应用

    何良1, 谭彩萍1, 曹乾1, 毛宗万1,2*
作者信息 +

Application of Phosphorescent Cyclometalated Iridium(Ⅲ) Complexes in Cancer Treatment

  • Liang He1, Caiping Tan1, Qian Cao1, Zongwan Mao1,2*
Author information +
文章历史 +

摘要

配位饱和且取代惰性的环金属化铱(Ⅲ)配合物由于优秀的磷光特性,在生物成像和生物传感等方面有着广泛的应用。近年来,该类铱配合物由于有效的抗肿瘤效力和新颖的抗肿瘤机制,在抗肿瘤方面的应用也引起了广泛关注。本文主要对磷光环金属化铱(Ⅲ)配合物(结构通式为[Ir(C^N)2(N^N)]+)在抗癌化疗和光动力治疗两方面的最新研究进展进行了综述;分类总结了靶向不同细胞器,作为蛋白-蛋白相互作用抑制剂,以及应用于单光子和双光子光动力治疗的环金属化铱(Ⅲ)配合物,为开发新型金属抗肿瘤药物提供参考。最后,对环金属化铱(Ⅲ)配合物在抗癌应用方面的前景进行了展望。

Abstract

Due to the excellent phosphorescent properties, the coordinatively saturated and substitutionally inert cyclometalated iridium(Ⅲ) complexes have been widely used in biological imaging and biosensing. In recent years, the application of this kind of iridium(Ⅲ) complexes in cancer treatment has attracted wide attention due to its anticancer efficacy and novel mechanisms. Recent advances of phosphorescent cyclometalated iridium(Ⅲ) complexes of the formula [Ir(C^N)2(N^N)]+ in anticancer chemotherapy and photodynamic therapy (PDT) are reviewed in this article. The iridium(Ⅲ) complexes targeting different organelles or as protein-protein interactions inhibitors or being applied in one-photon and two-photon PDT are summarized and discussed, which provides guidance for the development of new metal-based anticancer drugs. Finally, the development and application of phosphorescent cyclometalated iridium(Ⅲ) complexes in cancer treatment is discussed and prospected.
Contents
1 Introduction
2 Organelle-targeted phosphorescent anticancer cyclometalated iridium (Ⅲ) complexes
2.1 Mitochondria-targeted
2.2 Lysosome-targeted
2.3 Other organelles-targeted
3 Cyclometalated iridium(Ⅲ) complexes as protein-protein interactions inhibitors
4 Cyclometalated iridium(Ⅲ) complexes used in photodynamic therapy(PDT)
4.1 Mechanisms
4.2 One-photon PDT
4.3 Two-photon PDT
5 Conclusion and outlook

Graphical abstract

关键词

铱配合物 / 磷光 / 抗肿瘤 / 光动力治疗 / 诊疗

Key words

iridium complex / phosphorescence / anticancer / photodynamic therapy / theranostic

引用本文

引用格式 ▾
何良, 谭彩萍, 曹乾, 毛宗万. 磷光环金属化铱(Ⅲ)配合物在癌症治疗方面的应用[J]. 化学进展, 2018, 30(10): 1548-1556 DOI:10.7536/PC180610
Liang He, Caiping Tan, Qian Cao, Zongwan Mao. Application of Phosphorescent Cyclometalated Iridium(Ⅲ) Complexes in Cancer Treatment[J]. Progress in Chemistry, 2018, 30(10): 1548-1556 DOI:10.7536/PC180610

登录浏览全文

4963

注册一个新账户 忘记密码

参考文献

[1] Chen W Q, Zheng R S, Baade P D, Zhang S W, Zeng H M, Bray F, Jemal A, Yu X Q, He J. CA Cancer J. Clin., 2016, 66:115.
[2] Einhorn L H. J. Clin. Oncol., 1990, 8:1777.
[3] Jayson G C, Kohn E C, Kitchener H C, Ledermann J A. Lancet, 2014, 384:1376.
[4] Waggoner S E. Lancet, 2003, 361:2217.
[5] Argyriou A A, Polychronopoulos P, Iconomou G, Chroni E, Kalofonos H P. Cancer Treat. Rev., 2008, 34:368.
[6] Zhang C X, Lippard S J. Curr. Opin. Chem. Biol., 2003, 7:481.
[7] Kaluderovic G N, Paschke R. Curr. Med. Chem., 2011, 18:4738.
[8] van Rijt S H, Sadler P J. Drug Discov. Today, 2009, 14:1089.
[9] Fricker S P. Dalton Trans., 2007, 43:4903.
[10] Komeda S, Casini A. Curr. Top. Med. Chem., 2012, 12:219.
[11] Ma D L, He H Z, Leung K H, Chan D S, Leung C H. Angew. Chem. Int. Ed., 2013, 52:7666.
[12] Leung C H, Zhong H J, Chan D S H, Ma D L. Coord. Chem. Rev., 2013, 257:1764.
[13] Zhao Q, Huang C H, Li F Y. Chem. Soc. Rev., 2011, 40:2508.
[14] Lo K K W, Zhang K Y. Rsc Adv., 2012, 2:12069.
[15] You Y M, Cho S, Nam W W. Inorg. Chem., 2014, 53:1804.
[16] Zamora A, Vigueras G, Rodríguez V, Santana M D, Ruiz J. Coord. Chem. Rev., 2018, 360:34.
[17] You Y M. J. Chin. Chem. Soc., 2018, 65:352.
[18] Gao R M, Ho D G, Hernandez B, Selke M, Murphy D, Djurovich P I, Thompson M E. J. Am. Chem. Soc., 2002, 124:14828.
[19] You Y M. Curr. Opin. Chem. Biol., 2013, 17:699.
[20] Ma D L, Chan D S, Leung C H. Acc. Chem. Res., 2014, 47:3614.
[21] Vyas S, Zaganjor E, Haigis M C. Cell, 2016, 166:555.
[22] Fulda S, Galluzzi L, Kroemer G. Nat. Rev. Drug Discov., 2010, 9:447.
[23] Cao J J, Tan C P, Chen M H, Wu N, Yao D Y, Liu X G, Ji L N, Mao Z W. Chem. Sci., 2017, 8:631.
[24] Ye R R, Tan C P, Ji L N, Mao Z W. Dalton Trans., 2016, 45:13042.
[25] Youle R J, Narendra D P. Nat. Rev. Mol. Cell Biol., 2011, 12:9.
[26] Chen M H, Wang F X, Cao J J, Tan C P, Ji L N, Mao Z W. ACS Appl. Mater. Interfaces, 2017, 9:13304.
[27] Ye R R, Cao J J, Tan C P, Ji L N, Mao Z W. Chem. -Eur. J., 2017, 23:15166.
[28] He L, Wang K N, Zheng Y, Cao J J, Zhang M F, Tan C P, Ji L N, Mao Z W. Dalton Trans., 2018, 47:6942.
[29] Ouyang M, Zeng L L, Huang H Y, Jin C Z, Liu J P, Chen Y, Ji L N, Chao H. Dalton Trans., 2017, 46:6734.
[30] Weerasinghe P, Buja L M. Exp. Mol. Pathol., 2012, 93:302.
[31] Guan R L, Chen Y, Zeng L L, Rees T W, Jin C Z, Huang J J, Chen Z S, Ji L N, Chao H. Chem. Sci., 2018,9:5183.
[32] Venkatesh V, Berrocal-Martin R, Wedge C J, Romero-Canelon I, Sanchez-Cano C, Song J I, Coverdale J P C, Zhang P, Clarkson G J, Habtemariam A, Magennis S W, Deeth R J, Sadler P J. Chem. Sci., 2017, 8:8271.
[33] Saftig P, Sandhoff K. Nature, 2013, 502:312.
[34] Li S P Y, Tang T S M, Yiu K S M, Lo K K W. Chem. -Eur. J., 2012, 18:13342.
[35] He L, Liao S Y, Tan C P, Lu Y Y, Xu C X, Ji L N, Mao Z W. Chem. Commun., 2014, 50:5611.
[36] He L, Tan C P, Ye R R, Zhao Y Z, Liu Y H, Zhao Q, Ji L N, Mao Z W. Angew. Chem. Int. Ed., 2014, 53:12137.
[37] Cao R, Jia J L, Ma X C, Zhou M, Fei H. J. Med. Chem., 2013, 56:3636.
[38] Yellol J, Perez S A, Yellol G, Zajac J, Donaire A, Vigueras G, Novohradsky V, Janiak C, Brabec V, Ruiz J. Chem. Commun., 2016, 52:14165.
[39] Novohradsky V, Zamora A, Gandioso A, Brabec V, Ruiz J, Marchan V. Chem. Commun., 2017, 53:5523.
[40] Pracharova J, Vigueras G, Novohradsky V, Cutillas N, Janiak C, Kostrhunova H, Kasparkova J, Ruiz J, Brabec V. Chem. -Eur. J., 2018, 24:4607.
[41] Gamba I, Salvadó I, Brissos R F, Gamez P, Brea J, Loza M I, Vázquez M E, Vázquez López M. Chem. Commun., 2016, 52:1234.
[42] Salvadó I, Gamba I, Montenegro J, Martinez-Costas J, Brea J M, Loza M I, Vázquez López M, Vázquez M E. Chem. Commun., 2016, 52:11008.
[43] Scott D E, Bayly A R, Abell C, Skidmore J. Nat. Rev. Drug Discov., 2016, 15:533.
[44] Leung C H, Zhong H J, Yang H, Cheng Z, Chan D S, Ma V P, Abagyan R, Wong C Y, Ma D L. Angew. Chem. Int. Ed., 2012, 51:9010.
[45] Zhong H J, Lu L H, Leung K H, Wong C C L, Peng C, Yan S C, Ma D L, Cai Z W, Wang H M D, Leung C H. Chem. Sci., 2015, 6:5400.
[46] Liu L J, Wang W, Huang S Y, Hong Y, Li G, Lin S, Tian J, Cai Z, Wang H D, Ma D L, Leung C H. Chem. Sci., 2017, 8:4756.
[47] Liu L J, He B, Miles J A, Wang W, Mao Z, Che W I, Lu J J, Chen X P, Wilson A J, Ma D L, Leung C H. Oncotarget, 2016, 7:13965.
[48] Dolmans D E, Fukumura D, Jain R K. Nat. Rev. Cancer, 2003, 3:380.
[49] Agostinis P, Berg K, Cengel K A, Foster T H, Girotti A W, Gollnick S O, Hahn S M, Hamblin M R, Juzeniene A, Kessel D, Korbelik M, Moan J, Mroz P, Nowis D, Piette J, Wilson B C, Golab J. CA Cancer J. Clin., 2011, 61:250.
[50] You Y M, Nam W W. Chem. Soc. Rev., 2012, 41:7061.
[51] Jiang X P, Zhu N B, Zhao D H, Ma Y G. Sci. China Chem., 2016, 59, 40.
[52] Lerch M M, Hansen M J, van Dam G M, Szymanski W, Feringa B L. Angew. Chem. Int. Ed., 2016, 55:10978.
[53] Li S P, Lau C T, Louie M W, Lam Y W, Cheng S H, Lo K K. Biomaterials, 2013, 34:7519.
[54] Moromizato S, Hisamatsu Y, Suzuki T, Matsuo Y, Abe R, Aoki S. Inorg. Chem., 2012, 51:12697.
[55] Kando A, Hisamatsu Y, Ohwada H, Itoh T, Moromizato S, Kohno M, Aoki S. Inorg. Chem., 2015, 54:5342.
[56] He L, Li Y, Tan C P, Ye R R, Chen M H, Cao J J, Ji L N, Mao Z W. Chem. Sci., 2015, 6:5409.
[57] Ye R R, Tan C P, He L, Chen M H, Ji L N, Mao Z W. Chem. Commun., 2014, 50:10945.
[58] Jing Y, Cao Q, Hao L, Yang G G, Hu W L, Ji L N, Mao Z W. Chem. Commun., 2018, 54:271.
[59] Lv W, Zhang Z, Zhang K Y, Yang H, Liu S, Xu A, Guo S, Zhao Q, Huang W. Angew. Chem. Int. Ed., 2016, 55:9947.
[60] Gu B, Wu W B, Xu G X, Feng G X, Yin F, Chong P H J, Qu J L, Yong K T, Liu B. Adv. Mater., 2017, 29:1701076.
[61] Boreham E M, Jones L, Swinburne A N, Blanchard-Desce M, Hugues V, Terryn C, Miomandre F, Lemercier G, Natrajan L S. Dalton Trans., 2015, 44:16127.
[62] Nam J S, Kang M G, Kang J, Park S Y, Lee S J C, Kim H T, Seo J K, Kwon O H, Lim M H, Rhee H W, Kwon T H. J. Am. Chem. Soc., 2016, 138:10968.
[63] McKenzie L K, Sazanovich I V, Baggaley E, Bonneau M, Guerchais V, Williams J A, Weinstein J A, Bryant H E. Chem. -Eur. J., 2017, 23:234.
[64] Tian X H, Zhu Y H, Zhang M Z, Luo L, Wu J Y, Zhou H P, Guan L J, Battaglia G, Tian Y P. Chem. Commun., 2017, 53:3303.
[65] Liu J P, Jin C Z, Yuan B, Liu X G, Chen Y, Ji L N, Chao H. Chem. Commun., 2017, 53:2052.
PDF (1629KB)

2711

访问

0

被引

详细

导航
相关文章

/

〈 〉