Synlett 2023; 34(18): 2129-2158
DOI: 10.1055/a-2132-1356
account
Modern Boron Chemistry: 60 Years of the Matteson Reaction

Boronic Acids and Beyond: ROS-Responsive Prodrugs as Tools for a Safer and More Effective Cancer Chemotherapy

Sofia A. G. Monteiro
,
Pedro M. P. Gois
,
This work was generously supported by the Portuguese Fundação para a Ciência e Tecnologia, Ministério da Ciência e da Tecnologia, Portugal [grants, 2022.06817.CEECIND (J.A.), PTDC/QUI-OUT/ 3989/2021 (P.G.); Institutional grants UIDB/04138/2020 and UIDP/04138/2020 (iMed)].


Abstract

Despite significant scientific advances and the wide variety of available treatments, cancer remains a major cause of death worldwide. Chemotherapy, which is frequently one of the first-line treatments, frequently suffers from low selectivity to cancer cells, leading to the appearance of important side effects. Thus, it becomes imperative to develop a new generation of targeted alternatives that spare the healthy tissues by delivering the cytotoxic payloads safely and selectively to cancer cells. In this respect, prodrugs that are activated by tumor-specific stimuli have attracted significant attention. Despite being a hallmark of cancer and present in high concentrations in cancer cells, reactive oxygen species (ROS) have been rather underexplored as a stimulus for the preparation of targeted prodrugs, particularly when compared with an acidic pH or glutathione. Despite their lower expression, ROS have recently been gaining substantial consideration, with various ROS-responsive prodrugs already reported with meaningful performances both in vitro and in vivo. This review aims to provide critical insights into this strategy by discussing the various available functional groups (with an important focus on boronic acids and their esters), their mechanisms of action, examples of their applications, advantages, limitations, and future challenges.

1 Introduction

2 Boronic Acids and Boronate Esters

2.1 Histone Deacetylase Inhibitors

2.2 DNA Alkylating Agents

2.3 Selective Estrogen Receptor Modulators and Selective Estrogen Receptor Degraders

2.4 ROS Inducers

2.5 Prodrugs Based on Other Types of Anticancer Drugs

3 Other ROS-Responsive Moieties

3.1 Thiazolidinones

3.2 1,3-Oxathiolanes

3.3 Selenium Ethers

3.4 Sulfur-Containing ROS-Responsive Moieties

4 Summary and Future Perspectives



Publication History

Received: 14 June 2023

Accepted after revision: 18 July 2023

Accepted Manuscript online:
18 July 2023

Article published online:
05 September 2023

© 2023. Thieme. All rights reserved

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References and Notes

  • 1 Cancer . World Health Organization; Geneva: 2023. https://www.who.int/news-room/fact-sheets/detail/cancer (accessed Aug 23, 2023)
  • 2 Overview: Cancer . NHS; London: 2023. https://www.nhs.uk/conditions/cancer/ (accessed Aug 23, 2023)
  • 3 Patrick GL. An Introduction to Medicinal Chemistry, 5th ed. Oxford University Press; Oxford: 2013
  • 4 Hagen H, Marzenell P, Jentzsch E, Wenz F, Veldwijk MR, Mokhir A. J. Med. Chem. 2012; 55: 924
  • 5 Chemotherapy to Treat Cancer . National Cancer Institute; Bethesda: 2022. https://www.cancer.gov/about-cancer/treatment/types/chemotherapy (accessed Aug 23, 2023)
  • 6 Zhang X, Li X, You Q, Zhang X. Eur. J. Med. Chem. 2017; 139: 542
  • 7 Souza C, Pellosi DS, Tedesco AC. Expert Rev. Anticancer Ther. 2019; 19: 483
  • 8 Rautio J, Kumpulainen H, Heimbach T, Oliyai R, Oh D, Järvinen T, Savolainen J. Nat. Rev. Drug Discovery 2008; 7: 255
  • 9 Rautio J, Meanwell NA, Di L, Hageman MJ. Nat. Rev. Drug Discovery 2018; 17: 559
  • 10 Maslah H, Skarbek C, Pethe S, Labruère R. Eur. J. Med. Chem. 2020; 207: 112670
  • 11 Peng X, Gandhi V. Ther. Delivery 2012; 3: 823
  • 12 Wang P, Gong Q, Hu J, Li X, Zhang X. J. Med. Chem. 2021; 64: 298
  • 13 Ye H, Zhou Y, Liu X, Chen Y, Duan S, Zhu R, Liu Y, Yin L. Biomacromolecules 2019; 20: 2441
  • 14 Trachootham D, Alexandre J, Huang P. Nat. Rev. Drug Discovery 2009; 8: 579
  • 15 Saravanakumar G, Kim J, Kim WJ. Adv. Sci. (Weinheim, Ger.) 2017; 4: 1600124
  • 16 Papot S, Tranoy I, Tillequin F, Florent J.-C, Gesson J.-P. Curr. Med. Chem. 2002; 2: 155
  • 17 Al-Omari MK, Elaarag M, Al-Zoubi RM, Al-Qudimat AR, Zarour AA, Al-Hurani EA, Fares ZE, Alkharraz LM, Shkoor M, Bani-Yaseen AD, Aboumarzouk OM, Yassin A, Al-Ansari AA. J. Enzyme Inhib. Med. Chem. 2023; 38: 2220084
  • 18 Liang J, Liu B. Bioeng. Transl. Med. 2016; 1: 239
  • 19 Ballance WC, Qin EC, Chung HJ, Gillette MU, Kong H. Biomaterials 2019; 217: 119292
  • 20 Gao F, Xiong Z. Front. Chem. 2021; 9: 649048
  • 21 Liu J, Jia B, Li Z, Li W. Front. Bioeng. Biotechnol. 2023; 11: 1115603
  • 22 Messner K, Vuong B, Tranmer GK. Pharmaceuticals 2022; 15: 264
  • 23 Silva MP, Saraiva L, Pinto M, Sousa ME. Molecules 2020; 25: 4323
  • 24 Saxon E, Peng X. ChemBioChem 2022; 23: e202100366
  • 25 Boronic Acids: Preparation and Applications in Organic Synthesis, Medicine and Materials. Hall DG. Wiley-VCH; Weinheim: 2011
  • 26 Jiménez-Aligaga K, Bermejo-Bescós P, Martín-Aragón S, Csákÿ AG. Bioorg. Med. Chem. Lett. 2013; 23: 426
  • 27 Hiller N. deJ, do Amaral e Silva NA, Tavares TA, Faria RX, Nogueira Eberlin M, de Lun Martins D. Eur. J. Org. Chem. 2020; 4841
  • 28 Frankland E, Duppa B. Proc. R. Soc. London 1860; 10: 568
  • 29 Lennox AJ. J, Lloyd-Jones GC. Chem. Soc. Rev. 2013; 43: 412
  • 30 Gosecki M, Gosecka M. Polymers (Basel, Switz.) 2022; 14: 842
  • 31 Miyaura N, Suzuki A. Chem. Rev. 1995; 95: 2457
  • 32 António JP. M, Russo R, Carvalho CP, Cal PM. S. D, Gois PM. P. Chem. Soc. Rev. 2019; 48: 3513
  • 33 Peiró Cadahía J, Previtali V, Troelsen NS, Clausen MH. MedChemComm 2019; 10: 1531
  • 34 Chen J.-W, Wu T.-C, Liang W, Ciou J.-J, Lai C.-H. Drug Delivery Transl. Res. 2022; 13: 1305
  • 35 Kennedy L, Sandhu JK, Harper M.-E, Cuperlovic-Culf M. Biomolecules 2020; 10: 1429
  • 36 Cao S, Wang Y, Peng X. Chem. Eur. J. 2012; 18: 3850
  • 37 Cao S, Christiansen R, Peng X. Chem. Eur. J. 2013; 19: 9050
  • 38 Cao S, Wang Y, Peng X. J. Org. Chem. 2014; 79: 501
  • 39 Wang Y, Fan H, Balakrishnan K, Lin Z, Cao S, Chen W, Fan Y, Guthrie QA, Sun H, Teske KA, Gandhi V, Arnold LA, Peng X. Eur. J. Med. Chem. 2017; 133: 197
  • 40 Uversky VN. In Brenner’s Encyclopedia of Genetics, 2nd ed. Maloy S, Hughes K. Elsevier; Amsterdam: 2013: 425
  • 41 Vaissière T, Sawan C, Herceg Z. Mutat. Res. 2008; 659: 40
  • 42 Ni X, Li L, Pan G. Oncol. Lett. 2015; 9: 515
  • 43 Daniel KB, Sullivan ED, Chen Y, Chan JC, Jennings PA, Fierke CA, Cohen SM. J. Med. Chem. 2015; 58: 4812
  • 44 Hull EE, Montgomery MR, Leyva KJ. BioMed Res. Int. 2016; 8797206 DOI: 10.1155/2016/8797206.
  • 45 Kavianpour P, Gemmell MC. M, Kahlert JU, Rendina LM. ChemBioChem 2020; 21: 2786
  • 46 Bhagat SD, Singh U, Mishra RK, Srivastava A. ChemMedChem 2018; 13: 2073
  • 47 Li Y, Seto E. Cold Spring Harbor Perspect. Med. 2016; 6: a026831
  • 48 Zheng S, Guo S, Zhong Q, Zhang C, Liu J, Yang L, Zhang Q, Wang G. ACS Med. Chem. Lett. 2018; 9: 149
  • 49 Fed. Regist. FR Doc. 2022-06182, 2022
  • 50 Liao Y, Xu L, Ou S, Edwards H, Luedtke D, Ge Y, Qin Z. ACS Med. Chem. Lett. 2018; 9: 635
  • 51 Sreerama L. In Encyclopedia of Cancer, 3rd ed. Schwab M. Springer; Berlin: 2011: 132
  • 52 Lehmann F, Wennerberg J. Processes 2021; 9: 377
  • 53 Finch GL, Burns-Naas LA. In Encyclopedia of Toxicology, 3rd ed. Wexler P. Academic Press; London: 2014: 630
  • 54 Colvin OM. In Encyclopedia of Cancer, 2nd ed. Schwab M. Springer; Berlin: 2009: 35
  • 55 Chen W, Balakrishnan K, Kuang Y, Han Y, Fu M, Gandhi V, Peng X. J. Med. Chem. 2014; 57: 4498
  • 56 Singh RK, Kumar S, Prasad DN, Bhardwaj TR. Eur. J. Med. Chem. 2018; 151: 401
  • 57 Colvin M. In Holland-Frei Cancer Medicine, 6th ed., Chap. 51. Kufe D, Pollock RE, Weichselbaum RR, Bast RC, Gansler TS, Holland JF, Frei E. B. C. Decker; Hamilton: 2003
  • 58 Kuang Y, Balakrishnan K, Gandhi V, Peng X. J. Am. Chem. Soc. 2011; 133: 19278
  • 59 Chen W, Han Y, Peng X. Chem. Eur. J. 2014; 20: 7410
  • 60 Chen W, Fan H, Balakrishnan K, Wang Y, Sun H, Fan Y, Gandhi V, Arnold LA, Peng X. J. Med. Chem. 2018; 61: 9132
  • 61 Di Antonio M, Doria F, Richter SN, Bertipaglia C, Mella M, Sissi C, Palumbo M, Freccero M. J. Am. Chem. Soc. 2009; 131: 13132
  • 62 Pande P, Shearer J, Yang J, Greenberg WA, Rokita SE. J. Am. Chem. Soc. 1999; 121: 6773
  • 63 Patel HK, Bihani T. Pharmacol. Ther. 2018; 186: 1
  • 64 Hormone Therapy for Breast Cancer Fact Sheet§#/ITL#§. National Cancer Institute; Bethesda: 2022. (accessed Aug 23, 2023) https://www.cancer.gov/types/breast/breast-hormone-therapy-fact-sheet
  • 65 Liu J, Zheng S, Akerstrom VL, Yuan C, Ma Y, Zhong Q, Zhang C, Zhang Q, Guo S, Ma P, Skripnikova EV, Bratton MR, Pannuti A, Miele L, Wiese TE, Wang G. J. Med. Chem. 2016; 59: 8134
  • 66 Jiang Q, Zhong Q, Zhang Q, Zheng S, Wang G. ACS Med. Chem. Lett. 2012; 3: 392
  • 67 Zhong Q, Zhang C, Zhang Q, Miele L, Zheng S, Wang G. BMC Cancer 2015; 15: 625
  • 68 Zhang C, Zhong Q, Zhang Q, Zheng S, Miele L, Wang G. Breast Cancer Res. 2015; 152: 283
  • 69 Zhang C, Guo S, Yang L, Liu J, Zheng S, Zhong Q, Zhang Q, Wang G. Oncotarget 2017; 8: 103874
  • 70 Liu J, Zheng S, Guo S, Zhang C, Zhong Q, Zhang Q, Ma P, Skripnikova EV, Bratton MR, Wiese TE, Wang G. ACS Med. Chem. Lett. 2017; 8: 102
  • 71 Noh J, Kwon B, Han E, Park M, Yang W, Cho W, Yoo W, Khang G, Lee D. Nat. Commun. 2015; 6: 6907
  • 72 Liu Y, Liu H, Wang L, Wang Y, Zhang C, Wang C, Yan Y, Fan J, Xu G, Zhang Q. Nanoscale 2020; 2: 3872
  • 73 Fang J, Nakamura H, Iyer AK. J. Drug Targeting 2007; 15: 475
  • 74 Reshetnikov V, Daum S, Janko C, Karawacka W, Tietze R, Alexiou C, Paryzhak S, Dumych T, Bilyy R, Tripal P, Schmid B, Palmisano R, Mokhir A. Angew. Chem. Int. Ed. 2018; 57: 11943
  • 75 Reshetnikov V, Daum S, Mokhir A. Chem. Eur. J. 2017; 23: 5678
  • 76 Reshetnikov V, Arkhypov A, Julakanti PR, Mokhir A. Dalton Trans. 2018; 47: 6679
  • 77 Marzenell P, Hagen H, Sellner L, Zenz T, Grinyte R, Pavlov V, Daum S, Mokhir A. J. Med. Chem. 2013; 56: 6935
  • 78 Schikora M, Reznikov A, Chaykovskaya L, Sachinska O, Polyakova L, Mokhir A. Bioorg. Med. Chem. Lett. 2015; 25: 3447
  • 79 Daum S, Chekhun VF, Todor IN, Lukianova NY, Shvets YV, Sellner L, Putzker K, Lewis J, Zenz T, de Graaf IA. M, Groothuis GM. M, Casini A, Zozulia O, Hampel F, Mokhir A. J. Med. Chem. 2015; 58: 2015
  • 80 Daum S, Reshetnikov MS. V, Sisa M, Dumych T, Lootsik MD, Bilyy R, Bila E, Janko C, Alexiou C, Herrmann M, Sellner L, Mokhir A. Angew. Chem. Int. Ed. 2017; 56: 15545
  • 81 Daum S, Babiy S, Konovalova H, Hofer W, Shtemenko A, Shtemenko N, Janko C, Alexiou C, Mokhir A. J. Inorg. Biochem. 2018; 178: 9
  • 82 Reshetnikov V, Özkan HG, Daum S, Janko C, Alexiou C, Sauer C, Heinrich MR, Mokhir A. Molecules 2020; 25: 2545
  • 83 Xu H.-G, Schikora M, Sisa M, Daum S, Klemt I, Janko C, Alexiou C, Bila G, Bilyy R, Gong W, Schmitt M, Sellner L, Mokhir A. Angew. Chem. Int. Ed. 2021; 60: 11158
  • 84 Xu H.-G, Annamadov S, Mokhir A. J. Organomet. Chem. 2022; 964: 122305
  • 85 Pan Q, Zhang B, Peng X, Wan S, Luo K, Gao W, Pu Y, He B. Chem. Commun. 2019; 55: 13896
  • 86 Bao X.-Z, Wang Q, Ren X.-R, Dai F, Zhou B. Free Radical Biol. Med. 2020; 597
  • 87 Dewick PM. Medicinal Natural Products: A Biosynthetic Approach, 3rd ed. Wiley; Chichester: 2009: 380
  • 88 Wang L, Xie S, Ma L, Chen Y, Lu W. Eur. J. Med. Chem. 2016; 116: 84
  • 89 Wall ME, Wani MC, Cook CE, Palmer KH, McPhail AT, Sim GA. J. Am. Chem. Soc. 1966; 88: 3888
  • 90 Ai Y, Obianom ON, Kuser M, Li Y, Shu Y, Xue F. ACS Med. Chem. Lett. 2019; 10: 127
  • 91 Ghafouri-Fard S, Abak A, Anamag FT, Shoorei H, Fattahi F, Javadinia SA, Basiri A, Taheri M. Front. Oncol. 2021; 11: 658636 DOI: 10.3389/fonc.2021.658636.
  • 92 Matsushita K, Okuda T, Mori S, Konno M, Eguchi H, Asai A, Koseki J, Iwagami Y, Yamada D, Akita H, Asaoka T, Noda T, Kawamoto K, Gotoh K, Kobayashi S, Kasahara Y, Morihiro K, Satoh T, Doki Y, Mori M, Ishii H, Obika S. ChemMedChem 2019; 14: 1384
  • 93 Martino R, Gilard V, Malet-Martino M. In NMR Spectroscopy in Pharmaceutical Analysis . Holzgrabe U, Wawer I, Diehl B. Elsevier; Amsterdam: 2008: 369
  • 94 Waks AG, Winer EP. In The Breast: Comprehensive Management of Benign and Malignant Diseases, 5th ed. Bland KI, Copeland EM. III. Saunders Elsevier; Philadelphia: 2009: 885
  • 95 Skarbek C, Serra S, Maslah H, Rascol E, Labruère R. Bioorg. Chem. 2019; 91: 103158
  • 96 Dewick PM. Medicinal Natural Products: A Biosynthetic Approach, 3rd ed. Wiley; Chichester: 2009: 129
  • 97 Bielec B, Poetsch I, Ahmed E, Heffeter P, Keppler BK, Kowol CR. Molecules 2020; 25: 1149
  • 98 Yang X.-Y, Yuan B, Xiong H, Zhao Y, Wang L, Zhang S.-Q, Mao S. Bioorg. Chem. 2022; 129: 106154
  • 99 António JP. M, Carvalho JI, André AS, Dias JN. R, Aguiar SI, Faustino H, Lopes RM. R. M, Veiros LF, Bernardes GJ. L, da Silva FA, Gois PM. P. Angew. Chem. Int. Ed. 2021; 60: 25914
  • 100 Nirwan S, Chahal V, Kakkar R. J. Heterocycl. Chem. 2019; 56: 1239
  • 101 Liaras K, Fesatidou M, Geronikaki A. Molecules 2018; 23: 685
  • 102 Perez C, Monserrat J.-P, Chen Y, Cohen SM. Chem. Commun. 2015; 51: 7116
  • 103 Andersen NS, Peiró Cadahía J, Previtali V, Bondebjerg J, Hansen CA, Hansen AE, Andresen TL, Clausen MH. Eur. J. Med. Chem. 2018; 156: 738
  • 104 Lu M, Zhang X, Zhao J, You Q, Jiang Z. Redox Biol. 2020; 34: 101565
  • 105 Daniel KB, Major Jourden JL, Negoescu KE, Cohen SM. JBIC, J. Biol. Inorg. Chem. 2011; 16: 313
  • 106 Won M, Kim JH, Ji MS, Kim JS. Chem. Commun. 2022; 58: 72
  • 107 Fernandes AP, Gandin V. Biochim. Biophys. Acta, Gen. Subj. 2015; 1850: 1642
  • 108 Sharma AK, Amin S. Future Med. Chem. 2013; 5: 163
  • 109 Pan Z, Zhang J, Ji K, Chittavong V, Ji X, Wang B. Org. Lett. 2018; 20: 8
  • 110 Criado-Gonzalez M, Mecerreyes D. J. Mater. Chem. B 2022; 10: 7206
  • 111 Bohrer A.-S, Takahashi H. Int. Rev. Cell Mol. Biol. 2016; 326: 1
  • 112 Maeda H, Fukuyasu Y, Yoshida S, Fukuda M, Saeki K, Matsuno H, Yamauchi Y, Yoshida K, Hirata K, Miyamoto K. Angew. Chem. Int. Ed. 2004; 43: 2389
  • 113 Maeda H, Yamamoto K, Nomura Y, Kohno I, Hafsi L, Ueda N, Yoshida S, Fukuda M, Fukuyasu Y, Yamauchi Y, Itoh N. J. Am. Chem. Soc. 2005; 127: 68
  • 114 Xu K, Tang B, Huang H, Yang G, Chen Z, Li P, An L. Chem. Commun. 2005; 5974
  • 115 Rinaldi A, Caraffi R, Grazioli MV, Oddone N, Giardino L, Tosi G, Vandelli MA, Calzà L, Ruozi B, Duskey JT. Polymers (Basel, Switz.) 2022; 14: 687
  • 116 El-Mohtadi F, d’Arcy R, Tirelli N. Macromol. Rapid Commun. 2019; 40: 1800699
  • 117 Liu B, Thayumanavan S. Cell Reports Phys. Sci. 2020; 1: 100271
  • 118 Liu L.-H, Qiu W.-X, Li B, Zhang C, Sun L.-F, Wan S.-S, Rong L, Zhang X.-Z. Adv. Funct. Mater. 2016; 26: 6257
  • 119 Ma J, Chen Y, Liang W, Li L, Du J, Pan C, Zhang C. Drug Delivery 2021; 28: 1204
  • 120 Kim Y.-S, Kim S, Kang HC, Shim MS. J. Ind. Eng. Chem. 2019; 75: 238
  • 121 Yang J, Lv Q, Wei W, Yang Z, Dong J, Zhang R, Kan Q, He Z, Xu Y. Drug Delivery 2018; 25: 807
  • 122 Luo C, Sun J, Liu D, Sun B, Miao L, Musetti S, Li J, Han X, Du Y, Li L, Huang L, He Z. Nano Lett. 2016; 16: 5401
  • 123 Liu M, Luo Y, Yan J, Xiong X, Xing X, Kim JS, Zou T. J. Am. Chem. Soc. 2023; 145: 10082