메뉴 건너뛰기




Volumn 246, Issue , 2017, Pages 39-45

Linker stability influences the anti-tumor activity of acetazolamide-drug conjugates for the therapy of renal cell carcinoma

Author keywords

Drug release; Renal cell carcinoma; Small molecule drug conjugates; Targeted pro drugs; Therapy studies; Tumor targeting

Indexed keywords

AMINO ACIDS; CARBONIC ANHYDRASE; CELLS; CONTROLLED DRUG DELIVERY; CYTOLOGY; INFRARED DEVICES; MAMMALS; MOLECULES; PEPTIDES; SULFUR COMPOUNDS; THERMOGRAPHY (IMAGING); TUMORS;

EID: 85006959898     PISSN: 01683659     EISSN: 18734995     Source Type: Journal    
DOI: 10.1016/j.jconrel.2016.11.023     Document Type: Article
Times cited : (58)

References (56)
  • 2
    • 48149102140 scopus 로고    scopus 로고
    • Evaluation of biodistribution and anti-tumor effect of a dimeric RGD peptide-paclitaxel conjugate in mice with breast cancer
    • [2] Cao, Q., Li, Z.-B., Chen, K., Wu, Z., He, L., Neamati, N., Chen, X., Evaluation of biodistribution and anti-tumor effect of a dimeric RGD peptide-paclitaxel conjugate in mice with breast cancer. Eur. J. Nucl. Med. Mol. Imaging 35 (2008), 1489–1498.
    • (2008) Eur. J. Nucl. Med. Mol. Imaging , vol.35 , pp. 1489-1498
    • Cao, Q.1    Li, Z.-B.2    Chen, K.3    Wu, Z.4    He, L.5    Neamati, N.6    Chen, X.7
  • 4
    • 77955312203 scopus 로고    scopus 로고
    • Antibody-drug conjugates: targeted drug delivery for cancer
    • [4] Alley, S.C., Okeley, N.M., Senter, P.D., Antibody-drug conjugates: targeted drug delivery for cancer. Curr. Opin. Chem. Biol. 14 (2010), 529–537.
    • (2010) Curr. Opin. Chem. Biol. , vol.14 , pp. 529-537
    • Alley, S.C.1    Okeley, N.M.2    Senter, P.D.3
  • 5
    • 84879591299 scopus 로고    scopus 로고
    • The antibody-drug conjugate: an enabling modality for natural product-based cancer therapeutics
    • [5] Gerber, H.-P., Koehnb, F.E., Abraham, R.T., The antibody-drug conjugate: an enabling modality for natural product-based cancer therapeutics. Nat. Prod. Rep. 30 (2013), 625–639.
    • (2013) Nat. Prod. Rep. , vol.30 , pp. 625-639
    • Gerber, H.-P.1    Koehnb, F.E.2    Abraham, R.T.3
  • 6
    • 84898066972 scopus 로고    scopus 로고
    • Antibody-drug conjugates: an emerging concept in cancer therapy
    • [6] Chari, R.V.J., Miller, M.L., Widdison, W.C., Antibody-drug conjugates: an emerging concept in cancer therapy. Angew. Chem. Int. Ed. 53 (2014), 3796–3827.
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 3796-3827
    • Chari, R.V.J.1    Miller, M.L.2    Widdison, W.C.3
  • 7
    • 84874866559 scopus 로고    scopus 로고
    • Antibody-drug conjugates for the treatment of B-cell non-Hodgkin's lymphoma and leukemia
    • [7] Chu, Y.-W., Polson, A., Antibody-drug conjugates for the treatment of B-cell non-Hodgkin's lymphoma and leukemia. Future Oncol. 9 (2013), 355–368.
    • (2013) Future Oncol. , vol.9 , pp. 355-368
    • Chu, Y.-W.1    Polson, A.2
  • 8
    • 33947304452 scopus 로고    scopus 로고
    • The pharmacokinetics and pharmacodynamics of monoclonal antibodies–mechanistic modeling applied to drug development
    • [8] Mould, D.R., Sweeney, K.R.D., The pharmacokinetics and pharmacodynamics of monoclonal antibodies–mechanistic modeling applied to drug development. Curr. Opin. Drug Discov. Devel. 10 (2007), 84–96.
    • (2007) Curr. Opin. Drug Discov. Devel. , vol.10 , pp. 84-96
    • Mould, D.R.1    Sweeney, K.R.D.2
  • 10
    • 84962366882 scopus 로고    scopus 로고
    • Effects of antibody, drug and linker on the preclinical and clinical toxicities of antibody-drug conjugates
    • [10] Donaghy, H., Effects of antibody, drug and linker on the preclinical and clinical toxicities of antibody-drug conjugates. mAbs 8 (2016), 659–671.
    • (2016) mAbs , vol.8 , pp. 659-671
    • Donaghy, H.1
  • 12
    • 84968901405 scopus 로고    scopus 로고
    • Where did the linker-payload go? A quantitative investigation on the destination of the releasedlinker-payload from an antibody-drug conjugate with a maleimide linker in plasma
    • (4979–486)
    • [12] Wei, C., Zhang, G., Clark, T., Barletta, F., Tumey, L.N., Rago, B., Hansel, S., Han, X., Where did the linker-payload go? A quantitative investigation on the destination of the releasedlinker-payload from an antibody-drug conjugate with a maleimide linker in plasma. Anal. Chem., 88, 2016 (4979–486).
    • (2016) Anal. Chem. , vol.88
    • Wei, C.1    Zhang, G.2    Clark, T.3    Barletta, F.4    Tumey, L.N.5    Rago, B.6    Hansel, S.7    Han, X.8
  • 13
    • 84948845426 scopus 로고    scopus 로고
    • Antibody-drug conjugates and small molecule-drug conjugates: opportunities and challenges for the development of selective anticancer cytotoxic agents
    • [13] Casi, G., Neri, D., Antibody-drug conjugates and small molecule-drug conjugates: opportunities and challenges for the development of selective anticancer cytotoxic agents. J. Med. Chem. 58 (2015), 8751–8761.
    • (2015) J. Med. Chem. , vol.58 , pp. 8751-8761
    • Casi, G.1    Neri, D.2
  • 15
    • 71949089489 scopus 로고    scopus 로고
    • Real time, noninvasive imaging and quantitation of the accumulation of ligand-targeted drugs into receptor-expressing solid tumors
    • [15] Vlashi, E., Sturgis, J.E., Thomas, M., Low, P.S., Real time, noninvasive imaging and quantitation of the accumulation of ligand-targeted drugs into receptor-expressing solid tumors. Mol. Pharm. 6 (2009), 1868–1875.
    • (2009) Mol. Pharm. , vol.6 , pp. 1868-1875
    • Vlashi, E.1    Sturgis, J.E.2    Thomas, M.3    Low, P.S.4
  • 16
    • 67249157547 scopus 로고    scopus 로고
    • Prostate-specific membrane antigen targeted imaging and therapy of prostate cancer using a PSMA inhibitor as a homing ligand
    • [16] Kularatne, S.A., Wang, K., Santhapuram, H.K.R., Low, P.S., Prostate-specific membrane antigen targeted imaging and therapy of prostate cancer using a PSMA inhibitor as a homing ligand. Mol. Pharm. 6 (2009), 780–789.
    • (2009) Mol. Pharm. , vol.6 , pp. 780-789
    • Kularatne, S.A.1    Wang, K.2    Santhapuram, H.K.R.3    Low, P.S.4
  • 17
    • 77957921048 scopus 로고    scopus 로고
    • Folate-targeted therapies for cancer
    • [17] Xia, W., Low, P.S., Folate-targeted therapies for cancer. J. Med. Chem. 53 (2010), 6811–6824.
    • (2010) J. Med. Chem. , vol.53 , pp. 6811-6824
    • Xia, W.1    Low, P.S.2
  • 18
    • 84863946983 scopus 로고    scopus 로고
    • Engineering folate-drug conjugates to target cancer: from chemistry to clinic
    • [18] Vlahov, I.R., Leamon, C.P., Engineering folate-drug conjugates to target cancer: from chemistry to clinic. Bioconjug. Chem. 23 (2012), 1357–1369.
    • (2012) Bioconjug. Chem. , vol.23 , pp. 1357-1369
    • Vlahov, I.R.1    Leamon, C.P.2
  • 20
    • 35548944383 scopus 로고    scopus 로고
    • Targeted therapy of breast and gynecological cancers with cytotoxic analogues of peptide hormones
    • [20] Engel, J.B., Schally, A.V., Dietl, J., Rieger, L., Hönig, A., Targeted therapy of breast and gynecological cancers with cytotoxic analogues of peptide hormones. Mol. Pharm. 4 (2007), 652–658.
    • (2007) Mol. Pharm. , vol.4 , pp. 652-658
    • Engel, J.B.1    Schally, A.V.2    Dietl, J.3    Rieger, L.4    Hönig, A.5
  • 21
    • 84924094144 scopus 로고    scopus 로고
    • Principles in the design of ligand-targeted cancer therapeutics and imaging agents
    • [21] Srinivasarao, M., Galliford, C.V., Low, P.S., Principles in the design of ligand-targeted cancer therapeutics and imaging agents. Nat. Rev. Drug Discov. 14 (2015), 203–219.
    • (2015) Nat. Rev. Drug Discov. , vol.14 , pp. 203-219
    • Srinivasarao, M.1    Galliford, C.V.2    Low, P.S.3
  • 22
    • 33750082400 scopus 로고    scopus 로고
    • Targeting tumor-associated carbonic anhydrase IX in cancer therapy
    • [22] Thiry, A., Dogne, J.M., Masereel, B., Supuran, C.T., Targeting tumor-associated carbonic anhydrase IX in cancer therapy. Trends Pharmacol. Sci. 27 (2006), 566–573.
    • (2006) Trends Pharmacol. Sci. , vol.27 , pp. 566-573
    • Thiry, A.1    Dogne, J.M.2    Masereel, B.3    Supuran, C.T.4
  • 23
    • 26844517863 scopus 로고    scopus 로고
    • Carbonic anhydrase IX (CA IX) as a potential target for cancer therapy
    • [23] Pastorekova, S., Zavada, J., Carbonic anhydrase IX (CA IX) as a potential target for cancer therapy. Cancer Ther. 2 (2004), 245–262.
    • (2004) Cancer Ther. , vol.2 , pp. 245-262
    • Pastorekova, S.1    Zavada, J.2
  • 24
    • 84867818496 scopus 로고    scopus 로고
    • Inhibition of carbonic anhydrase IX as a novel anticancer mechanism
    • [24] Supuran, C.T., Inhibition of carbonic anhydrase IX as a novel anticancer mechanism. World J. Clin. Oncol. 7 (2012), 98–103.
    • (2012) World J. Clin. Oncol. , vol.7 , pp. 98-103
    • Supuran, C.T.1
  • 27
    • 84979282978 scopus 로고    scopus 로고
    • Evaluation of nonpeptidic ligand conjugates for SPECT imaging of hypoxic and carbonic anhydrase IX-expressing cancers
    • [27] Lv, P.-C., Putt, K.S., Low, P.S., Evaluation of nonpeptidic ligand conjugates for SPECT imaging of hypoxic and carbonic anhydrase IX-expressing cancers. Bioconjug. Chem. 27 (2016), 1762–1769.
    • (2016) Bioconjug. Chem. , vol.27 , pp. 1762-1769
    • Lv, P.-C.1    Putt, K.S.2    Low, P.S.3
  • 28
    • 84975093395 scopus 로고    scopus 로고
    • Darwinian dynamics of intratumoral heterogeneity: not solely random mutations but also variable environmental selection forces
    • [28] Lloyd, M.C., Cunningham, J.J., Bui, M.M., Gillies, R.J., Brown, J.S., Gatenby, R.A., Darwinian dynamics of intratumoral heterogeneity: not solely random mutations but also variable environmental selection forces. Cancer Res. 76 (2016), 3136–3144.
    • (2016) Cancer Res. , vol.76 , pp. 3136-3144
    • Lloyd, M.C.1    Cunningham, J.J.2    Bui, M.M.3    Gillies, R.J.4    Brown, J.S.5    Gatenby, R.A.6
  • 30
    • 84898627356 scopus 로고    scopus 로고
    • A small-molecule drug conjugate for the treatment of carbonic anhydrase IX expressing tumors
    • [30] Krall, N., Pretto, F., Decurtins, W., Bernardes, G.J.L., Supuran, C.T., Neri, D., A small-molecule drug conjugate for the treatment of carbonic anhydrase IX expressing tumors. Angew. Chem. Int. Ed. 53 (2014), 4231–4235.
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 4231-4235
    • Krall, N.1    Pretto, F.2    Decurtins, W.3    Bernardes, G.J.L.4    Supuran, C.T.5    Neri, D.6
  • 31
    • 85008368535 scopus 로고    scopus 로고
    • Acetazolamide serves as selective delivery vehicle for dipeptide-linked drugs to renal cell carcinoma
    • [31] Cazzamalli, S., Dal Corso, A., Neri, D., Acetazolamide serves as selective delivery vehicle for dipeptide-linked drugs to renal cell carcinoma. Mol. Cancer Ther., 2016, 10.1158/1535-7163.MCT-16-0283.
    • (2016) Mol. Cancer Ther.
    • Cazzamalli, S.1    Dal Corso, A.2    Neri, D.3
  • 32
    • 84905172017 scopus 로고    scopus 로고
    • A bivalent small molecule-drug conjugate directed against carbonic anhydrase IX can elicit complete tumour regression in mice
    • [32] Krall, N., Pretto, F., Neri, D., A bivalent small molecule-drug conjugate directed against carbonic anhydrase IX can elicit complete tumour regression in mice. Chem. Sci. 5 (2014), 3640–3644.
    • (2014) Chem. Sci. , vol.5 , pp. 3640-3644
    • Krall, N.1    Pretto, F.2    Neri, D.3
  • 33
    • 84973635769 scopus 로고    scopus 로고
    • A 99mTc-labeled ligand of carbonic anhydrase IX selectively targets renal cell carcinoma in vivo
    • [33] Krall, N., Pretto, F., Mattarella, M., Müller, C., Neri, D., A 99mTc-labeled ligand of carbonic anhydrase IX selectively targets renal cell carcinoma in vivo. J. Nucl. Med. 57 (2016), 943–949.
    • (2016) J. Nucl. Med. , vol.57 , pp. 943-949
    • Krall, N.1    Pretto, F.2    Mattarella, M.3    Müller, C.4    Neri, D.5
  • 34
    • 84900002772 scopus 로고    scopus 로고
    • Curative properties of noninternalizing antibody-drug conjugates based on maytansinoids
    • [34] Perrino, E., Steiner, M., Krall, N., Bernardes, G.J.L., Pretto, F., Casi, G., Neri, D., Curative properties of noninternalizing antibody-drug conjugates based on maytansinoids. Cancer Res. 74 (2014), 2569–2578.
    • (2014) Cancer Res. , vol.74 , pp. 2569-2578
    • Perrino, E.1    Steiner, M.2    Krall, N.3    Bernardes, G.J.L.4    Pretto, F.5    Casi, G.6    Neri, D.7
  • 35
    • 84958150818 scopus 로고    scopus 로고
    • Antibody format and drug release rate determine the therapeutic activity of noninternalizing antibody-drug conjugates
    • [35] Gébleux, R., Wulhfard, S., Casi, G., Neri, D., Antibody format and drug release rate determine the therapeutic activity of noninternalizing antibody-drug conjugates. Mol. Cancer Ther. 14 (2015), 2606–2612.
    • (2015) Mol. Cancer Ther. , vol.14 , pp. 2606-2612
    • Gébleux, R.1    Wulhfard, S.2    Casi, G.3    Neri, D.4
  • 36
    • 84908606333 scopus 로고    scopus 로고
    • Disulfide-containing parenteral delivery systems and their redox-biological fate
    • [36] Brülisauer, L., Gauthier, M.A., Leroux, J.-C., Disulfide-containing parenteral delivery systems and their redox-biological fate. J. Control. Release 195 (2014), 147–154.
    • (2014) J. Control. Release , vol.195 , pp. 147-154
    • Brülisauer, L.1    Gauthier, M.A.2    Leroux, J.-C.3
  • 37
    • 84934442221 scopus 로고    scopus 로고
    • Antibody-drug conjugate target selection: critical factors
    • [37] Bander, N.H., Antibody-drug conjugate target selection: critical factors. Methods Mol. Biol. 1045 (2013), 29–40.
    • (2013) Methods Mol. Biol. , vol.1045 , pp. 29-40
    • Bander, N.H.1
  • 38
    • 84943581649 scopus 로고    scopus 로고
    • Internalization, trafficking, intracellular processing and actions of antibody-drug conjugates
    • [38] Xu, S., Internalization, trafficking, intracellular processing and actions of antibody-drug conjugates. Pharm. Res. 32 (2015), 3577–3583.
    • (2015) Pharm. Res. , vol.32 , pp. 3577-3583
    • Xu, S.1
  • 41
    • 0036074253 scopus 로고    scopus 로고
    • Cathepsin B-labile dipeptide linkers for lysosomal release of doxorubicin from internalizing immunoconjugates: model studies of enzymatic drug release and antigen-specific in vitro anticancer activity
    • [41] Dubowchik, G.M., Firestone, R.A., Padilla, L., Willner, D., Hofstead, S.J., Mosure, K., Knipe, J.O., Lasch, S.J., Trail, P.A., Cathepsin B-labile dipeptide linkers for lysosomal release of doxorubicin from internalizing immunoconjugates: model studies of enzymatic drug release and antigen-specific in vitro anticancer activity. Bioconjug. Chem. 13 (2002), 855–869.
    • (2002) Bioconjug. Chem. , vol.13 , pp. 855-869
    • Dubowchik, G.M.1    Firestone, R.A.2    Padilla, L.3    Willner, D.4    Hofstead, S.J.5    Mosure, K.6    Knipe, J.O.7    Lasch, S.J.8    Trail, P.A.9
  • 42
  • 43
    • 84934298082 scopus 로고    scopus 로고
    • Sequence of treatment in locally advanced and metastatic renal cell carcinoma
    • [43] Fischer, S., Gillessen, S., Rothermundt, C., Sequence of treatment in locally advanced and metastatic renal cell carcinoma. Transl. Androl. Urol. 4 (2015), 310–325.
    • (2015) Transl. Androl. Urol. , vol.4 , pp. 310-325
    • Fischer, S.1    Gillessen, S.2    Rothermundt, C.3
  • 46
    • 84921763721 scopus 로고    scopus 로고
    • Drug radiotherapy combinations: review of previous failures and reasons for future optimism
    • [46] Higgins, G.S., O'Cathail, S.M., Muschel, R.J., McKenna, W.G., Drug radiotherapy combinations: review of previous failures and reasons for future optimism. Cancer Treat. Rev. 41 (2015), 105–113.
    • (2015) Cancer Treat. Rev. , vol.41 , pp. 105-113
    • Higgins, G.S.1    O'Cathail, S.M.2    Muschel, R.J.3    McKenna, W.G.4
  • 47
    • 84958843614 scopus 로고    scopus 로고
    • Combining antibody-drug conjugates and immune-mediated cancer therapy: What to expect?
    • [47] Gerber, H.-P., Sapra, P., Loganzo, F., May, C., Combining antibody-drug conjugates and immune-mediated cancer therapy: What to expect?. Biochem. Pharmacol. 102 (2016), 1–6.
    • (2016) Biochem. Pharmacol. , vol.102 , pp. 1-6
    • Gerber, H.-P.1    Sapra, P.2    Loganzo, F.3    May, C.4
  • 48
    • 0032402354 scopus 로고    scopus 로고
    • Cathepsin B-sensitive dipeptide prodrugs. 1. A model study of structural requirements for efficient release of doxorubicin
    • [48] Dubowchik, G.M., Firestone, R.A., Cathepsin B-sensitive dipeptide prodrugs. 1. A model study of structural requirements for efficient release of doxorubicin. Bioorg. Med. Chem. Lett., 1998, 3341–3346.
    • (1998) Bioorg. Med. Chem. Lett. , pp. 3341-3346
    • Dubowchik, G.M.1    Firestone, R.A.2
  • 50
    • 84863688504 scopus 로고    scopus 로고
    • The discovery and development of brentuximab vedotin for use in relapsed Hodgkin lymphoma and systemic anaplastic large cell lymphoma
    • [50] Senter, P.D., Sievers, E.L., The discovery and development of brentuximab vedotin for use in relapsed Hodgkin lymphoma and systemic anaplastic large cell lymphoma. Nat. Biotechnol. 30 (2012), 631–637.
    • (2012) Nat. Biotechnol. , vol.30 , pp. 631-637
    • Senter, P.D.1    Sievers, E.L.2
  • 51
    • 84902655584 scopus 로고    scopus 로고
    • Dual targeting of integrin αvβ3 and matrix metalloproteinase-2 for optical imaging of tumors and chemotherapeutic delivery
    • [51] Crisp, J.L., Savariar, E.N., Glasgow, H.L., Ellies, L.G., Whitney, M.A., Tsien, R.Y., Dual targeting of integrin αvβ3 and matrix metalloproteinase-2 for optical imaging of tumors and chemotherapeutic delivery. Mol. Cancer Ther. 13 (2014), 1514–1525.
    • (2014) Mol. Cancer Ther. , vol.13 , pp. 1514-1525
    • Crisp, J.L.1    Savariar, E.N.2    Glasgow, H.L.3    Ellies, L.G.4    Whitney, M.A.5    Tsien, R.Y.6
  • 52
    • 78649300912 scopus 로고    scopus 로고
    • Conjugates of a novel 7-substituted camptothecin with RGD-peptides as αvβ3 integrin ligands: an approach to tumor-targeted therapy
    • [52] Dal Pozzo, A., Esposito, E., Ni, M., Muzi, L., Pisano, C., Bucci, F., Vesci, L., Castorina, M., Penco, S., Conjugates of a novel 7-substituted camptothecin with RGD-peptides as αvβ3 integrin ligands: an approach to tumor-targeted therapy. Bioconjug. Chem. 21 (2010), 1956–1967.
    • (2010) Bioconjug. Chem. , vol.21 , pp. 1956-1967
    • Dal Pozzo, A.1    Esposito, E.2    Ni, M.3    Muzi, L.4    Pisano, C.5    Bucci, F.6    Vesci, L.7    Castorina, M.8    Penco, S.9
  • 53
    • 84866334630 scopus 로고    scopus 로고
    • Development of novel bisphosphonate prodrugs of doxorubicin for targeting bone metastases that are cleaved pH dependently or by cathepsin B: synthesis, cleavage properties, and binding properties to hydroxyapatite as well as bone matrix
    • [53] Hochdörffer, K., Abu Ajaj, K., Schäfer-Obodozie, C., Kratz, F., Development of novel bisphosphonate prodrugs of doxorubicin for targeting bone metastases that are cleaved pH dependently or by cathepsin B: synthesis, cleavage properties, and binding properties to hydroxyapatite as well as bone matrix. J. Med. Chem. 55 (2012), 7502–7515.
    • (2012) J. Med. Chem. , vol.55 , pp. 7502-7515
    • Hochdörffer, K.1    Abu Ajaj, K.2    Schäfer-Obodozie, C.3    Kratz, F.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.