Abstract
The rapidly developing field of cancer treatment requires versatile strategies for controlled drug delivery and diagnostics. Molecular imaging technology has gained attraction in cancer diagnosis and therapy, partially driven by nanoparticle-based theranostic agents. Nanotheranostics-based imaging platforms offer insights into both malignancy diagnosis and therapeutic response monitoring. Monitoring body response to certain cancer treatment will offer suitable pathological and surgical evaluation guides to evaluate how tumors shrink/metastasize, as well as the side effects associated with the therapeutic approach. This chapter summarizes fundamental imaging features of nanotheranostics, specifically, treatment monitoring in cancer therapy, with applications in therapeutic monitoring, such as tracking angiogenesis, metastasis, and apoptosis, following primary treatment. This chapter also offers an outlook for future translation and clinical applications of such multifunctional nanoconstructs.
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References
Siegel, R.L., Miller, K.D., Jemal, A.: Cancer statistics, 2017. CA Cancer J. Clin. 67(1), 7–30 (2017). https://doi.org/10.3322/caac.21387
Smith, R.A., Andrews, K.S., Brooks, D., Fedewa, S.A., Manassaram-Baptiste, D., Saslow, D., Brawley, O.W., Wender, R.C.: Cancer screening in the United States, 2017: a review of current American Cancer Society guidelines and current issues in cancer screening. CA Cancer J. Clin. 67(2), 100–121 (2017). https://doi.org/10.3322/caac.21392
Lim, Z.-Z.J., Li, J.-E.J., Ng, C.-T., Yung, L.-Y.L., Bay, B.-H.: Gold nanoparticles in cancer therapy. Acta Pharmacol. Sin. 32(8), 983–990 (2011)
Walker, N.F., Gan, C., Olsburgh, J., Khan, M.S.: Diagnosis and management of intradiverticular bladder tumours. Nat. Rev. Urol. 11(7), 383–390 (2014). https://doi.org/10.1038/nrurol.2014.131
Carbone, A., Vaccher, E., Gloghini, A., Pantanowitz, L., Abayomi, A., de Paoli, P., Franceschi, S.: Diagnosis and management of lymphomas and other cancers in HIV-infected patients. Nat. Rev. Clin. Oncol. 11(4), 223–238 (2014). https://doi.org/10.1038/nrclinonc.2014.31
Liu, Z., Chen, X.: Simple bioconjugate chemistry serves great clinical advances: albumin as a versatile platform for diagnosis and precision therapy. Chem. Soc. Rev. (2016)
Choi, K.Y., Liu, G., Lee, S., Chen, X.: Theranostic nanoplatforms for simultaneous cancer imaging and therapy: current approaches and future perspectives. Nanoscale. 4(2), 330–342 (2012). https://doi.org/10.1039/c1nr11277e
Wang, J., Mi, P., Lin, G., Wáng, Y.X.J., Liu, G., Chen, X.: Imaging guided delivery of RNAi for anticancer treatment. Adv. Drug Deliv. Rev. (2016)
Miao, T., Rao, K.S., Spees, J.L., Floreani, R.A.: Osteogenic differentiation of human mesenchymal stem cells through alginate-graft-poly(ethylene glycol) microsphere-mediated intracellular growth factor delivery. J. Control. Release. 192, 57–66 (2014). https://doi.org/10.1016/j.jconrel.2014.06.029
Miao, T., Fenn, S.L., Charron, P.N., Floreani, R.A.: Self-healing and thermoresponsive dual-cross-linked alginate hydrogels based on supramolecular inclusion complexes. Biomacromolecules. 16(12), 3740–3750 (2015). https://doi.org/10.1021/acs.biomac.5b00940
Miao, T., Miller, E.J., McKenzie, C., Floreani, R.A.: Physically crosslinked polyvinyl alcohol and gelatin interpenetrating polymer network theta-gels for cartilage regeneration. J. Mater. Chem. B. 3(48), 9242–9249 (2015). https://doi.org/10.1039/C5TB00989H
O'Brien, F.J.: Biomaterials & scaffolds for tissue engineering. Mater. Today. 14(3), 88–95 (2011). https://doi.org/10.1016/S1369-7021(11)70058-X
Mura, S., Couvreur, P.: Nanotheranostics for personalized medicine. Adv. Drug Deliv. Rev. 64(13), 1394–1416 (2012). https://doi.org/10.1016/j.addr.2012.06.006
Liu, Y., Miyoshi, H., Nakamura, M.: Nanomedicine for drug delivery and imaging: a promising avenue for cancer therapy and diagnosis using targeted functional nanoparticles. Int. J. Cancer. 120(12), 2527–2537 (2007). https://doi.org/10.1002/ijc.22709
Chi, X., Huang, D., Zhao, Z., Zhou, Z., Yin, Z., Gao, J.: Nanoprobes for in vitro diagnostics of cancer and infectious diseases. Biomaterials. 33(1), 189–206 (2012). https://doi.org/10.1016/j.biomaterials.2011.09.032
Pirmohamed, M., Ferner, R.E.: Monitoring drug treatment. BMJ. 327(7425), 1179–1181 (2003)
Weissleder, R., Mahmood, U.: Molecular imaging. Radiology. 219(2), 316–333 (2001). https://doi.org/10.1148/radiology.219.2.r01ma19316
Bao, G., Mitragotri, S., Tong, S.: Multifunctional nanoparticles for drug delivery and molecular imaging. Annu. Rev. Biomed. Eng. 15, 253–282 (2013). https://doi.org/10.1146/annurev-bioeng-071812-152409
Cleary, K., Peters, T.M.: Image-guided interventions: technology review and clinical applications. Annu. Rev. Biomed. Eng. 12, 119–142 (2010). https://doi.org/10.1146/annurev-bioeng-070909-105249
Bhattarai, N., Bhattarai, S.R.: Theranostic nanoparticles: a recent breakthrough in nanotechnology. J. Nanomed. Nanotechnol. 2012, (2012)
Mody, V.V., Siwale, R., Singh, A., Mody, H.R.: Introduction to metallic nanoparticles. J. Pharm Bioall Sci. 2(4), 282–289 (2010). https://doi.org/10.4103/0975-7406.72127
Corr, S.A.: Metal oxide nanoparticles. In: Nanoscience: Volume 1: Nanostructures through Chemistry, vol. 1, pp. 180–207. The Royal Society of Chemistry, London, UK (2013). https://doi.org/10.1039/9781849734844-00180
Bangal, M., Ashtaputre, S., Marathe, S., Ethiraj, A., Hebalkar, N., Gosavi, S.W., Urban, J., Kulkarni, S.K.: Semiconductor nanoparticles. Hyperfine Interact. 160(1), 81–94 (2005). https://doi.org/10.1007/s10751-005-9151-y
Liberman, A., Mendez, N., Trogler, W.C., Kummel, A.C.: Synthesis and surface functionalization of silica nanoparticles for nanomedicine. Surf. Sci. Rep. 69(2-3), 132–158 (2014). https://doi.org/10.1016/j.surfrep.2014.07.001
Dinarvand, R., Sepehri, N., Manoochehri, S., Rouhani, H., Atyabi, F.: Polylactide-co-glycolide nanoparticles for controlled delivery of anticancer agents. Int. J. Nanomedicine. 6, 877–895 (2011). https://doi.org/10.2147/IJN.S18905
Guilherme, M.R., Mauricio, M.R., Tenório-Neto, E.T., Kunita, M.H., Cardozo-Filho, L., Cellet, T.S.P., Pereira, G.M., Muniz, E.C., da Rocha, S.R.P., Rubira, A.F.: Polycaprolactone nanoparticles containing encapsulated progesterone prepared using a scCO2 emulsion drying technique. Mater. Lett. 124, 197–200 (2014). https://doi.org/10.1016/j.matlet.2014.03.099
Langer, K., Anhorn, M.G., Steinhauser, I., Dreis, S., Celebi, D., Schrickel, N., Faust, S., Vogel, V.: Human serum albumin (HSA) nanoparticles: reproducibility of preparation process and kinetics of enzymatic degradation. Int. J. Pharm. 347(1–2), 109–117 (2008). https://doi.org/10.1016/j.ijpharm.2007.06.028
Cardoso, V.S., Quelemes, P.V., Amorin, A., Primo, F.L., Gobo, G.G., Tedesco, A.C., Mafud, A.C., Mascarenhas, Y.P., Corrêa, J.R., Kuckelhaus, S.A., Eiras, C., Leite, J.R.S., Silva, D., dos Santos Júnior, J.R.: Collagen-based silver nanoparticles for biological applications: synthesis and characterization. J. Nanobiotechnol. 12(1), 36 (2014). https://doi.org/10.1186/s12951-014-0036-6
Wicki, A., Witzigmann, D., Balasubramanian, V., Huwyler, J.: Nanomedicine in cancer therapy: challenges, opportunities, and clinical applications. J. Control. Release. 200, 138–157 (2015). https://doi.org/10.1016/j.jconrel.2014.12.030
Duncan, R., Gaspar, R.: Nanomedicine(s) under the microscope. Mol. Pharm. 8(6), 2101–2141 (2011). https://doi.org/10.1021/mp200394t
Brindle, K.: New approaches for imaging tumour responses to treatment. Nat. Rev. Cancer. 8(2), 94–107 (2008)
National Lung Screening Trial Research T: The National Lung Screening Trial: overview and study design. Radiology. 258(1), 243–253 (2011). https://doi.org/10.1148/radiol.10091808
Irion, K.L., Hochhegger, B., Marchiori, E., Porto, N.S., Baldisserotto, S.V., Santana, P.R.: Radiograma de tórax e tomografia computadorizada na avaliação do enfisema pulmonar. J. Bras. Pneumol. 33, 720–732 (2007)
McLaughlin, R., Hylton, N.: MRI in breast cancer therapy monitoring. NMR Biomed. 24(6), 712–720 (2011). https://doi.org/10.1002/nbm.1739
Avril, N.E., Weber, W.A.: Monitoring response to treatment in patients utilizing PET. Radiol. Clin. N. Am. 43(1), 189–204 (2005)
Cai, J., Li, F.: Single-photon emission computed tomography tracers for predicting and monitoring cancer therapy. Curr. Pharm. Biotechnol. 14(7), 693–707 (2013)
Falou, O., Sadeghi-Naini, A., Soliman, H., Yaffe, M.J., Czarnota, G.J.: Diffuse optical imaging for monitoring treatment response in breast cancer patients. Conf. Proc IEEE Eng. Med. Biol. Soc. 2012, 3155–3158 (2012). https://doi.org/10.1109/embc.2012.6346634
Hrkach, J., Von Hoff, D., Ali, M.M., Andrianova, E., Auer, J., Campbell, T., De Witt, D., Figa, M., Figueiredo, M., Horhota, A., Low, S., McDonnell, K., Peeke, E., Retnarajan, B., Sabnis, A., Schnipper, E., Song, J.J., Song, Y.H., Summa, J., Tompsett, D., Troiano, G., Van Geen Hoven, T., Wright, J., LoRusso, P., Kantoff, P.W., Bander, N.H., Sweeney, C., Farokhzad, O.C., Langer, R., Zale, S.: Preclinical development and clinical translation of a PSMA-targeted Docetaxel nanoparticle with a differentiated pharmacological profile. Sci. Transl. Med. 4(128), 128ra139-128ra139 (2012). https://doi.org/10.1126/scitranslmed.3003651
Janib, S.M., Moses, A.S., MacKay, J.A.: Imaging and drug delivery using theranostic nanoparticles. Adv. Drug Deliv. Rev. 62(11), 1052–1063 (2010). https://doi.org/10.1016/j.addr.2010.08.004
Villaraza, A.J.L., Bumb, A., Brechbiel, M.W.: Macromolecules, Dendrimers and Nanomaterials in magnetic resonance imaging: the interplay between size, function and pharmacokinetics. Chem. Rev. 110(5), 2921–2959 (2010). https://doi.org/10.1021/cr900232t
Kunjachan, S., Ehling, J., Storm, G., Kiessling, F., Lammers, T.: Noninvasive imaging of Nanomedicines and Nanotheranostics: principles, Progress, and prospects. Chem. Rev. (2015). https://doi.org/10.1021/cr500314d
Miao, T., Zhang, Y., Zeng, Y., Tian, R., Liu, G.: Functional nanoparticles for molecular imaging-guided gene delivery and therapy. In: Dai, Z. (ed.) Advances in Nanotheranostics II: Cancer Theranostic Nanomedicine, pp. 273–305. Springer Singapore, Singapore (2016). https://doi.org/10.1007/978-981-10-0063-8_8
Lu, J., Feng, F., Jin, Z.: Cancer diagnosis and treatment guidance: role of MRI and MRI probes in the era of molecular imaging. Curr. Pharm. Biotechnol. 14(8), 714–722 (2013)
Strijkers, G.J., Mulder, W.J., van Tilborg, G.A., Nicolay, K.: MRI contrast agents: current status and future perspectives. Anti Cancer Agents Med. Chem. 7(3), 291–305 (2007)
Su, H., Wu, C., Zhu, J., Miao, T., Wang, D., Xia, C., Zhao, X., Gong, Q., Song, B., Ai, H.: Rigid Mn(II) chelate as efficient MRI contrast agent for vascular imaging. Dalton Trans. 41(48), 14480–14483 (2012). https://doi.org/10.1039/c2dt31696j
Luo, K., Tian, J., Liu, G., Sun, J., Xia, C., Tang, H., Lin, L., Miao, T., Zhao, X., Gao, F., Gong, Q., Song, B., Shuai, X., Ai, H., Gu, Z.: Self-assembly of SiO2/Gd-DTPA-polyethylenimine nanocomposites as magnetic resonance imaging probes. J. Nanosci. Nanotechnol. 10(1), 540–548 (2010)
Phillips, W.T., Bao, A., Sou, K., Li, S., Goins, B.: Radiolabeled liposomes as drug delivery nanotheranostics. In: Drug Delivery Applications of Noninvasive Imaging, pp. 252–267. John Wiley & Sons, Inc, Hoboken, NJ, USA (2013). https://doi.org/10.1002/9781118356845.ch11
Luk, B.T., Fang, R.H., Zhang, L.: Lipid- and polymer-based nanostructures for cancer theranostics. Theranostics. 2(12), 1117–1126 (2012). https://doi.org/10.7150/thno.4381
Kaida, S., Cabral, H., Kumagai, M., Kishimura, A., Terada, Y., Sekino, M., Aoki, I., Nishiyama, N., Tani, T., Kataoka, K.: Visible drug delivery by supramolecular nanocarriers directing to single-platformed diagnosis and therapy of pancreatic tumor model. Cancer Res. 70(18), 7031–7041 (2010). https://doi.org/10.1158/0008-5472.can-10-0303
Yu, M.K., Jeong, Y.Y., Park, J., Park, S., Kim, J.W., Min, J.J., Kim, K., Jon, S.: Drug-loaded superparamagnetic iron oxide nanoparticles for combined cancer imaging and therapy in vivo. Angew. Chem. Int. Ed. Engl. 47(29), 5362–5365 (2008). https://doi.org/10.1002/anie.200800857
Ng, T.S., Wert, D., Sohi, H., Procissi, D., Colcher, D., Raubitschek, A.A., Jacobs, R.E.: Serial diffusion MRI to monitor and model treatment response of the targeted nanotherapy CRLX101. Clin. Cancer Res. 19(9), 2518–2527 (2013). https://doi.org/10.1158/1078-0432.ccr-12-2738
Folkman, J.: Tumor angiogenesis: therapeutic implications. N. Engl. J. Med. 285(21), 1182–1186 (1971). https://doi.org/10.1056/nejm197111182852108
Bergers, G., Hanahan, D.: Modes of resistance to anti-angiogenic therapy. Nat. Rev. Cancer. 8(8), 592–603 (2008). https://doi.org/10.1038/nrc2442
Wang, Z., Dabrosin, C., Yin, X., Fuster, M.M., Arreola, A., Rathmell, W.K., Generali, D., Nagaraju, G.P., El-Rayes, B., Ribatti, D., Chen, Y.C., Honoki, K., Fujii, H., Georgakilas, A.G., Nowsheen, S., Amedei, A., Niccolai, E., Amin, A., Ashraf, S.S., Helferich, B., Yang, X., Guha, G., Bhakta, D., Ciriolo, M.R., Aquilano, K., Chen, S., Halicka, D., Mohammed, S.I., Azmi, A.S., Bilsland, A., Keith, W.N., Jensen, L.D.: Broad targeting of angiogenesis for cancer prevention and therapy. Semin. Cancer Biol. 35, Supplement:S224–Supplement:S243 (2015). https://doi.org/10.1016/j.semcancer.2015.01.001
Cai, W., Chen, X.: Multimodality molecular imaging of tumor angiogenesis. J. Nucl. Med. 49(Suppl 2), 113S–128S (2008). https://doi.org/10.2967/jnumed.107.045922
Choyke, P.L., Dwyer, A.J., Knopp, M.V.: Functional tumor imaging with dynamic contrast-enhanced magnetic resonance imaging. J. Magn. Reson. Imaging. 17(5), 509–520 (2003). https://doi.org/10.1002/jmri.10304
O'Connor, J.P.B., Jackson, A., Parker, G.J.M., Jayson, G.C.: DCE-MRI biomarkers in the clinical evaluation of antiangiogenic and vascular disrupting agents. Br. J. Cancer. 96(2), 189–195 (2007). https://doi.org/10.1038/sj.bjc.6603515
Knopp, M.V., Weiss, E., Sinn, H.P., Mattern, J., Junkermann, H., Radeleff, J., Magener, A., Brix, G., Delorme, S., Zuna, I., van Kaick, G.: Pathophysiologic basis of contrast enhancement in breast tumors. J. Magn. Reson. Imaging. 10(3), 260–266 (1999)
Wang, B., Gao, Z.Q., Yan, X.: Correlative study of angiogenesis and dynamic contrast-enhanced magnetic resonance imaging features of hepatocellular carcinoma. Acta. Radiol. 46(4), 353–358 (2005)
Korpanty, G., Carbon, J.G., Grayburn, P.A., Fleming, J.B., Brekken, R.A.: Monitoring response to anticancer therapy by targeting microbubbles to tumor vasculature. Clin. Cancer Res. 13(1), 323–330 (2007). https://doi.org/10.1158/1078-0432.ccr-06-1313
Campbell, I.D., Humphries, M.J.: Integrin structure, activation, and interactions. Cold Spring Harb. Perspect. Biol. 3(3), (2011). https://doi.org/10.1101/cshperspect.a004994
Danhier, F., Le Breton, A., Preat, V.: RGD-based strategies to target alpha(v) beta(3) integrin in cancer therapy and diagnosis. Mol. Pharm. 9(11), 2961–2973 (2012). https://doi.org/10.1021/mp3002733
Tan, M., Lu, Z.-R.: Integrin targeted MR imaging. Theranostics. 1, 83–101 (2011)
Sipkins, D.A., Cheresh, D.A., Kazemi, M.R., Nevin, L.M., Bednarski, M.D., Li, K.C.: Detection of tumor angiogenesis in vivo by alphaVbeta3-targeted magnetic resonance imaging. Nat. Med. 4(5), 623–626 (1998)
Barrett, T., Brechbiel, M., Bernardo, M., Choyke, P.L.: MRI of tumor angiogenesis. J. Magn. Reson. Imaging. 26(2), 235–249 (2007). https://doi.org/10.1002/jmri.20991
Lecouvet, F.E., Talbot, J.N., Messiou, C., Bourguet, P., Liu, Y., de Souza, N.M.: Monitoring the response of bone metastases to treatment with Magnetic Resonance Imaging and nuclear medicine techniques: a review and position statement by the European Organisation for Research and Treatment of Cancer imaging group. Eur. J. Cancer. 50(15), 2519–2531 (2014). https://doi.org/10.1016/j.ejca.2014.07.002
Heyn, C., Ronald, J.A., Ramadan, S.S., Snir, J.A., Barry, A.M., MacKenzie, L.T., Mikulis, D.J., Palmieri, D., Bronder, J.L., Steeg, P.S., Yoneda, T., MacDonald, I.C., Chambers, A.F., Rutt, B.K., Foster, P.J.: In vivo MRI of cancer cell fate at the single-cell level in a mouse model of breast cancer metastasis to the brain. Magn. Reson. Med. 56(5), 1001–1010 (2006). https://doi.org/10.1002/mrm.21029
Steichen, S.D., Caldorera-Moore, M., Peppas, N.A.: A review of current nanoparticle and targeting moieties for the delivery of cancer therapeutics. Eur J. Pharm. Sci. 48(3), 416–427 (2013). https://doi.org/10.1016/j.ejps.2012.12.006
Elmore, S.: Apoptosis: a review of programmed cell death. Toxicol. Pathol. 35(4), 495–516 (2007). https://doi.org/10.1080/01926230701320337
Balcer-Kubiczek, E.K.: Apoptosis in radiation therapy: a double-edged sword. Exp. Oncol. 34(3), 277–285 (2012)
Kaufmann, S.H., Earnshaw, W.C.: Induction of apoptosis by cancer chemotherapy. Exp. Cell Res. 256(1), 42–49 (2000). https://doi.org/10.1006/excr.2000.4838
Mouratidis, P.X., Rivens, I., Ter Haar, G.: A study of thermal dose-induced autophagy, apoptosis and necroptosis in colon cancer cells. Int. J. Hyperthermia. 31(5), 476–488 (2015). https://doi.org/10.3109/02656736.2015.1029995
Panzarini, E., Tenuzzo, B., Dini, L.: Photodynamic therapy-induced apoptosis of HeLa cells. Ann. N. Y. Acad. Sci. 1171, 617–626 (2009). https://doi.org/10.1111/j.1749-6632.2009.04908.x
Zeng, W., Wang, X., Xu, P., Liu, G., Eden, H.S., Chen, X.: Molecular imaging of apoptosis: from micro to macro. Theranostics. 5(6), 559–582 (2015). https://doi.org/10.7150/thno.11548
Marino, G., Kroemer, G.: Mechanisms of apoptotic phosphatidylserine exposure. Cell Res. 23(11), 1247–1248 (2013). https://doi.org/10.1038/cr.2013.115
Blanco, V.M., Latif, T., Chu, Z., Qi, X.: Imaging and therapy of pancreatic cancer with phosphatidylserine-targeted nanovesicles. Transl. Oncol. 8(3), 196–203 (2015). https://doi.org/10.1016/j.tranon.2015.03.011
Jung, H.-i., Kettunen, M.I., Davletov, B., Brindle, K.M.: Detection of apoptosis using the C2A domain of synaptotagmin I. Bioconjug. Chem. 15(5), 983–987 (2004). https://doi.org/10.1021/bc049899q
Zhao, M., Beauregard, D.A., Loizou, L., Davletov, B., Brindle, K.M.: Non-invasive detection of apoptosis using magnetic resonance imaging and a targeted contrast agent. Nat. Med. 7(11), 1241–1244 (2001)
GarcÃa-Figueiras, R., Padhani, A.R., Baleato-González, S.: Therapy monitoring with functional and molecular MR imaging. Magn. Reson. Imaging Clin. N. Am. 24(1), 261–288 (2016). https://doi.org/10.1016/j.mric.2015.08.003
Schroeder, M.A., Clarke, K., Neubauer, S., Tyler, D.J.: Hyperpolarized magnetic resonance: a novel technique for the in vivo assessment of cardiovascular disease. Circulation. 124(14), 1580–1594 (2011). https://doi.org/10.1161/circulationaha.111.024919
van Zijl, P.C.M., Yadav, N.N.: Chemical exchange saturation transfer (CEST): what is in a name and what isn’t? Magn. Reson. Med. 65(4), 927–948 (2011). https://doi.org/10.1002/mrm.22761
O'Connor, J.P., Jackson, A., Parker, G.J., Roberts, C., Jayson, G.C.: Dynamic contrast-enhanced MRI in clinical trials of antivascular therapies. Nat. Rev. Clin. Oncol. 9(3), 167–177 (2012). https://doi.org/10.1038/nrclinonc.2012.2 http://www.nature.com/nrclinonc/journal/v9/n3/suppinfo/nrclinonc.2012.2_S1.html
Jacobson, O., Chen, X.: Interrogating tumor metabolism and tumor microenvironments using molecular positron emission tomography imaging. Theranostic approaches to improve therapeutics. Pharmacol. Rev. 65(4), 1214–1256 (2013). https://doi.org/10.1124/pr.113.007625
Nishimura, K., Hida, S., Nishio, Y., Ohishi, K., Okada, Y., Okada, K., Yoshida, O., Nishimura, K., Nishibuchi, S.: The validity of magnetic resonance imaging (MRI) in the staging of bladder cancer: comparison with computed tomography (CT) and transurethral ultrasonography (US). Jpn. J. Clin. Oncol. 18(3), 217–226 (1988)
Ryu, J.S., Kim, J.S., Moon, D.H., Kim, S.M., Shin, M.J., Chang, J.S., Park, S.K., Han, D.J., Lee, H.K.: Bone SPECT is more sensitive than MRI in the detection of early osteonecrosis of the femoral head after renal transplantation. J. Nucl. Med. 43(8), 1006–1011 (2002)
Spanaki, M.V., Spencer, S.S., Corsi, M., MacMullan, J., Seibyl, J., Zubal, I.G.: Sensitivity and specificity of quantitative difference SPECT analysis in seizure localization. J. Nucl. Med. 40(5), 730–736 (1999)
Wang, J., Maurer, L.: Positron emission tomography: applications in drug discovery and drug development. Curr. Top. Med. Chem. 5(11), 1053–1075 (2005)
Rahmim, A., Zaidi, H.: PET versus SPECT: strengths, limitations and challenges. Nucl. Med. Commun. 29(3), 193–207 (2008). https://doi.org/10.1097/MNM.0b013e3282f3a515
Malviya, G., Nayak, T.K.: PET imaging to monitor cancer therapy. Curr. Pharm. Biotechnol. 14(7), 669–682 (2013)
Jacobson, O., Weiss, I., Wang, L., Wang, Z., Yang, X., Dewhurst, A., Ma, Y., Zhu, G., Niu, G., Kiesewetter, D.O., Vasdev, N., Liang, S., Chen, X.: 18F-labeled single-stranded DNA aA. for PET imaging of protein tyrosine Kinase-7 expression. J. Nucl. Med. (2015). https://doi.org/10.2967/jnumed.115.160960
Weissleder, R.: Molecular imaging in cancer. Science (New York, N.Y.). 312(5777), 1168–1171 (2006). https://doi.org/10.1126/science.1125949
Quon, A., Gambhir, S.S.: FDG-PET and beyond: molecular breast cancer imaging. J. Clin Oncol. 23(8), 1664–1673 (2005). https://doi.org/10.1200/jco.2005.11.024
Avril, N., Sassen, S., Schmalfeldt, B., Naehrig, J., Rutke, S., Weber, W.A., Werner, M., Graeff, H., Schwaiger, M., Kuhn, W.: Prediction of response to neoadjuvant chemotherapy by sequential F-18-fluorodeoxyglucose positron emission tomography in patients with advanced-stage ovarian cancer. J. Clin Oncol. 23(30), 7445–7453 (2005). https://doi.org/10.1200/jco.2005.06.965
Yaghoubi, S.S., Gambhir, S.S.: PET imaging of herpes simplex virus type 1 thymidine kinase (HSV1-tk) or mutant HSV1-sr39tk reporter gene expression in mice and humans using [18F]FHBG. Nat. Protocols. 1(6), 3069–3074 (2007). http://www.nature.com/nprot/journal/v1/n6/suppinfo/nprot.2006.459_S1.html
Folkman, J.: Role of angiogenesis in tumor growth and metastasis. Semin. Oncol. 29(6 Suppl 16), 15–18 (2002). https://doi.org/10.1053/sonc.2002.37263
Weis, S.M., Cheresh, D.A.: αv integrins in angiogenesis and cancer. Cold Spring Harb. Perspect. Med. 1(1), a006478 (2011). https://doi.org/10.1101/cshperspect.a006478
Humphries, J.D., Byron, A., Humphries, M.J.: Integrin ligands at a glance. J. Cell Sci. 119(19), 3901–3903 (2006). https://doi.org/10.1242/jcs.03098
Haubner, R., Kuhnast, B., Mang, C., Weber, W.A., Kessler, H., Wester, H.J., Schwaiger, M.: [18F]Galacto-RGD: synthesis, radiolabeling, metabolic stability, and radiation dose estimates. Bioconjug. Chem. 15(1), 61–69 (2004). https://doi.org/10.1021/bc034170n
Niu, G., Chen, X.: RGD PET: from lesion detection to therapy response monitoring. J. Nucl. Med. (2015). https://doi.org/10.2967/jnumed.115.168278
Zheng, K., Liang, N., Zhang, J., Lang, L., Zhang, W., Li, S., Zhao, J., Niu, G., Li, F., Zhu, Z., Chen, X.: 68Ga-NOTA-PRGD2 PET/CT for integrin imaging in patients with lung cancer. J. Nucl. Med. 56(12), 1823–1827 (2015). https://doi.org/10.2967/jnumed.115.160648
Blankenberg, F.G., Katsikis, P.D., Tait, J.F., Davis, R.E., Naumovski, L., Ohtsuki, K., Kopiwoda, S., Abrams, M.J., Darkes, M., Robbins, R.C.: In vivo detection and imaging of phosphatidylserine expression during programmed cell death. Proc. Natl. Acad. Sci. 95(11), 6349–6354 (1998)
Kartachova, M., van Zandwijk, N., Burgers, S., van Tinteren, H., Verheij, M., Valdes Olmos, R.A.: Prognostic significance of 99mTc Hynic-rh-annexin V scintigraphy during platinum-based chemotherapy in advanced lung cancer. J. Clin. Oncol. 25(18), 2534–2539 (2007). https://doi.org/10.1200/jco.2006.10.1337
Koulov, A.V., Stucker, K.A., Lakshmi, C., Robinson, J.P., Smith, B.D.: Detection of apoptotic cells using a synthetic fluorescent sensor for membrane surfaces that contain phosphatidylserine. Cell Death Differ. 10(12), 1357–1359 (2003). https://doi.org/10.1038/sj.cdd.4401315
Kwong, J.M.K., Hoang, C., Dukes, R.T., Yee, R.W., Gray, B.D., Pak, K.Y., Caprioli, J.: Bis(Zinc-Dipicolylamine), Zn-DPA, a new marker for apoptosis. Invest. Ophthalmol. Vis. Sci. 55(8), 4913–4921 (2014). https://doi.org/10.1167/iovs.13-13346
Oltmanns, D., Zitzmann-Kolbe, S., Mueller, A., Bauder-Wuest, U., Schaefer, M., Eder, M., Haberkorn, U., Eisenhut, M.: Zn(II)-bis(cyclen) complexes and the imaging of apoptosis/necrosis. Bioconjug. Chem. 22(12), 2611–2624 (2011). https://doi.org/10.1021/bc200457b
Khalil, M.M., Tremoleda, J.L., Bayomy, T.B., Gsell, W.: Molecular SPECT imaging: an overview. Int. J. Molecul. Imag. 2011, (2011). https://doi.org/10.1155/2011/796025
Thorwarth, D.: Radiotherapy treatment planning based on functional PET/CT imaging data. Nucl. Med. Rev. 15(C), 43–47 (2012)
Currin, E., Linden, H.M., Mankoff, D.A.: Predicting breast Cancer endocrine responsiveness using molecular imaging. Curr. Breast Cancer Rep. 3(4), 205–211 (2011). https://doi.org/10.1007/s12609-011-0053-5
Sun, Y., Yang, Z., Zhang, Y., Xue, J., Wang, M., Shi, W., Zhu, B., Hu, S., Yao, Z., Pan, H., Zhang, Y.: The preliminary study of 16α-[18F]fluoroestradiol PET/CT in assisting the individualized treatment decisions of breast Cancer patients. PLoS One. 10(1), e0116341 (2015). https://doi.org/10.1371/journal.pone.0116341
Costas, B.: Review of biomedical optical imaging—a powerful, non-invasive, non-ionizing technology for improving in vivo diagnosis. Meas. Sci. Technol. 20(10), 104020 (2009)
Weissleder, R., Ntziachristos, V.: Shedding light onto live molecular targets. Nat. Med. 9(1), 123–128 (2003)
Kulkarni, A., Rao, P., Natarajan, S., Goldman, A., Sabbisetti, V.S., Khater, Y., Korimerla, N., Chandrasekar, V., Mashelkar, R.A., Sengupta, S.: Reporter nanoparticle that monitors its anticancer efficacy in real time. Proc. Natl. Acad. Sci. 113(15), E2104–E2113 (2016). https://doi.org/10.1073/pnas.1603455113
Kumar, R., Han, J., Lim, H.-J., Ren, W.X., Lim, J.-Y., Kim, J.-H., Kim, J.S.: Mitochondrial induced and self-monitored intrinsic apoptosis by antitumor Theranostic Prodrug: in vivo imaging and precise Cancer treatment. J. Am. Chem. Soc. 136(51), 17836–17843 (2014). https://doi.org/10.1021/ja510421q
Buchwalow, I.B., Böcker, W.: Antibodies for immunohistochemistry. In: Immunohistochemistry: Basics and Methods, pp. 1–8. Springer, New York City, NY, USA (2010)
Nune, S.K., Gunda, P., Thallapally, P.K., Lin, Y.-Y., Forrest, M.L., Berkland, C.J.: Nanoparticles for biomedical imaging. Expert Opin. Drug Deliv. 6(11), 1175–1194 (2009). https://doi.org/10.1517/17425240903229031
Kim, K., Kim, J.H., Park, H., Kim, Y.S., Park, K., Nam, H., Lee, S., Park, J.H., Park, R.W., Kim, I.S., Choi, K., Kim, S.Y., Park, K., Kwon, I.C.: Tumor-homing multifunctional nanoparticles for cancer theragnosis: simultaneous diagnosis, drug delivery, and therapeutic monitoring. J. Control. Release. 146(2), 219–227 (2010). https://doi.org/10.1016/j.jconrel.2010.04.004
Allison, R.R.: Photodynamic therapy: oncologic horizons. Future Oncol. 10(1), 123–124 (2014). https://doi.org/10.2217/fon.13.176
Luo, S., Tan, X., Fang, S., Wang, Y., Liu, T., Wang, X., Yuan, Y., Sun, H., Qi, Q., Shi, C.: Mitochondria-targeted small-molecule fluorophores for dual modal Cancer phototherapy. Adv. Funct. Mater. 26(17), 2826–2835 (2016). https://doi.org/10.1002/adfm.201600159
Wang, H., Chen, K., Niu, G., Chen, X.: Site-specifically biotinylated VEGF121 for near-infrared fluorescence imaging of tumor angiogenesis. Mol. Pharm. 6(1), 285–294 (2009). https://doi.org/10.1021/mp800185h
Lee, S., Chen, X.: Dual-modality probes for in vivo molecular imaging. Mol. Imaging. 8(2), 87–100 (2009)
Petrovsky, A., Schellenberger, E., Josephson, L., Weissleder, R., Bogdanov Jr., A.: Near-infrared fluorescent imaging of tumor apoptosis. Cancer Res. 63(8), 1936–1942 (2003)
Ntziachristos, V., Schellenberger, E.A., Ripoll, J., Yessayan, D., Graves, E., Bogdanov, A., Josephson, L., Weissleder, R.: Visualization of antitumor treatment by means of fluorescence molecular tomography with an annexin V–Cy5.5 conjugate. Proc. Natl. Acad. Sci. U. S. A. 101(33), 12294–12299 (2004). https://doi.org/10.1073/pnas.0401137101
Lee, S., Choi, K.Y., Chung, H., Ryu, J.H., Lee, A., Koo, H., Youn, I.-C., Park, J.H., Kim, I.-S., Kim, S.Y., Chen, X., Jeong, S.Y., Kwon, I.C., Kim, K., Choi, K.: Real time, high resolution video imaging of apoptosis in single cells with a polymeric nanoprobe. Bioconjug. Chem. 22(2), 125–131 (2011). https://doi.org/10.1021/bc1004119
Chi, C., Du, Y., Ye, J., Kou, D., Qiu, J., Wang, J., Tian, J., Chen, X.: Intraoperative imaging-guided cancer surgery: from current fluorescence molecular imaging methods to future multi-modality imaging technology. Theranostics. 4(11), 1072–1084 (2014). https://doi.org/10.7150/thno.9899
Vahrmeijer, A.L., Hutteman, M., van der Vorst, J.R., van de Velde, C.J.H., Frangioni, J.V.: Image-guided cancer surgery using near-infrared fluorescence. Nat. Rev. Clin. Oncol. 10(9), 507–518 (2013). https://doi.org/10.1038/nrclinonc.2013.123
Nguyen, Q.T., Tsien, R.Y.: Fluorescence-guided surgery with live molecular navigation [mdash] a new cutting edge. Nat. Rev. Cancer. 13(9), 653–662 (2013). https://doi.org/10.1038/nrc3566
van Dam, G.M., Themelis, G., Crane, L.M.A., Harlaar, N.J., Pleijhuis, R.G., Kelder, W., Sarantopoulos, A., de Jong, J.S., Arts, H.J.G., van der Zee, A.G.J., Bart, J., Low, P.S., Ntziachristos, V.: Intraoperative tumor-specific fluorescence imaging in ovarian cancer by folate receptor-[alpha] targeting: first in-human results. Nat. Med. 17(10), 1315–1319 (2011). http://www.nature.com/nm/journal/v17/n10/abs/nm.2472.html#supplementary-information
van der Vorst, J.R., Schaafsma, B.E., Hutteman, M., Verbeek, F.P., Liefers, G.J., Hartgrink, H.H., Smit, V.T., Lowik, C.W., van de Velde, C.J., Frangioni, J.V., Vahrmeijer, A.L.: Near-infrared fluorescence-guided resection of colorectal liver metastases. Cancer. 119(18), 3411–3418 (2013). https://doi.org/10.1002/cncr.28203
Sugie, T., Sawada, T., Tagaya, N., Kinoshita, T., Yamagami, K., Suwa, H., Ikeda, T., Yoshimura, K., Niimi, M., Shimizu, A., Toi, M.: Comparison of the indocyanine green fluorescence and blue dye methods in detection of sentinel lymph nodes in early-stage breast cancer. Ann. Surg. Oncol. 20(7), 2213–2218 (2013). https://doi.org/10.1245/s10434-013-2890-0
Kim, H.S., Ahn, J.H., Chung, H.H., Kim, J.W., Park, N.H., Song, Y.S., Lee, H.P., Kim, Y.B.: Impact of intraoperative rupture of the ovarian capsule on prognosis in patients with early-stage epithelial ovarian cancer: a meta-analysis. Eur. J. Surg. Oncol. 39(3), 279–289 (2013). https://doi.org/10.1016/j.ejso.2012.12.003
Azarpira, N., Asadi, N., Torabineghad, S., Taghipour, M.: Metastatic malignant melanoma intraoperative imprint cytology of brain tumor. J. Cytol. 29(3), 192–193 (2012). https://doi.org/10.4103/0970-9371.101170
Crane, L.M., Themelis, G., Arts, H.J., Buddingh, K.T., Brouwers, A.H., Ntziachristos, V., van Dam, G.M., van der Zee, A.G.: Intraoperative near-infrared fluorescence imaging for sentinel lymph node detection in vulvar cancer: first clinical results. Gynecol. Oncol. 120(2), 291–295 (2011). https://doi.org/10.1016/j.ygyno.2010.10.009
Baldauf, J., Muller, J.U., Fleck, S., Hinz, P., Chiriac, A., Schroeder, H.W.: The value of intraoperative three dimensional fluoroscopy in anterior decompressive surgery of the cervical spine. Zentralbl. Neurochir. 69(1), 30–34 (2008). https://doi.org/10.1055/s-2007-992796
Kircher, M.F., Mahmood, U., King, R.S., Weissleder, R., Josephson, L.: A multimodal nanoparticle for preoperative magnetic resonance imaging and intraoperative optical brain tumor delineation. Cancer Res. 63(23), 8122–8125 (2003)
Kircher, M.F., de la Zerda, A., Jokerst, J.V., Zavaleta, C.L., Kempen, P.J., Mittra, E., Pitter, K., Huang, R., Campos, C., Habte, F., Sinclair, R., Brennan, C.W., Mellinghoff, I.K., Holland, E.C., Gambhir, S.S.: A brain tumor molecular imaging strategy using a new triple-modality MRI-photoacoustic-Raman nanoparticle. Nat. Med. 18(5), 829–834 (2012). http://www.nature.com/nm/journal/v18/n5/abs/nm.2721.html#supplementary-information
Cherry, S.R.: Multimodality in vivo imaging systems: twice the power or double the trouble? Annu. Rev. Biomed. Eng. 8(1), 35–62 (2006). https://doi.org/10.1146/annurev.bioeng.8.061505.095728
Louie, A.: Multimodality imaging probes: design and challenges. Chem. Rev. 110(5), 3146–3195 (2010). https://doi.org/10.1021/cr9003538
Pomper, M.G., Gelovani, J.G.: Molecular Imaging in Oncology. Informa Health Care, New York (2008)
Ell, P.J.: The contribution of PET/CT to improved patient management. Br. J. Radiol. 79(937), 32–36 (2006). https://doi.org/10.1259/bjr/18454286
Tsukamoto, E., Ochi, S.: PET/CT today: system and its impact on cancer diagnosis. Ann. Nucl. Med. 20(4), 255–267 (2006)
Cherry, S.R., Louie, A.Y., Jacobs, R.E.: The integration of positron emission tomography with magnetic resonance imaging. Proc. IEEE. 96(3), 416–438 (2008)
Jarrett, B.R., Gustafsson, B., Kukis, D.L., Louie, A.Y.: Synthesis of (64)cu-labeled magnetic nanoparticles for multimodal imaging. Bioconjug. Chem. 19(7), 1496–1504 (2008). https://doi.org/10.1021/bc800108v
Lee, H.-Y., Li, Z., Chen, K., Hsu, A.R., Xu, C., Xie, J., Sun, S., Chen, X.: PET/MRI dual-modality tumor imaging using arginine-glycine-aspartic (RGD)–conjugated radiolabeled Iron oxide nanoparticles. J. Nucl. Med. 49(8), 1371–1379 (2008). https://doi.org/10.2967/jnumed.108.051243
Cai, W., Chen, K., Li, Z.B., Gambhir, S.S., Chen, X.: Dual-function probe for PET and near-infrared fluorescence imaging of tumor vasculature. J. Nucl. Med. 48(11), 1862–1870 (2007). https://doi.org/10.2967/jnumed.107.043216
Phillips, E., Penate-Medina, O., Zanzonico, P.B., Carvajal, R.D., Mohan, P., Ye, Y., Humm, J., Gönen, M., Kalaigian, H., Schöder, H., Strauss, H.W., Larson, S.M., Wiesner, U., Bradbury, M.S.: Clinical translation of an ultrasmall inorganic optical-PET imaging nanoparticle probe. Sci. Transl. Med. 6(260), 260ra149-260ra149 (2014). https://doi.org/10.1126/scitranslmed.3009524
Xie, R., Peng, X.: Synthesis of Cu-doped InP nanocrystals (d-dots) with ZnSe diffusion barrier as efficient and color-tunable NIR emitters. J. Am. Chem. Soc. 131(30), 10645–10651 (2009)
Wang, H.-F., He, Y., Ji, T.-R., Yan, X.-P.: Surface molecular imprinting on Mn-doped ZnS quantum dots for room-temperature phosphorescence optosensing of pentachlorophenol in water. Anal. Chem. 81(4), 1615–1621 (2009)
Santra, P.K., Kamat, P.V.: Mn-doped quantum dot sensitized solar cells: a strategy to boost efficiency over 5%. J. Am. Chem. Soc. 134(5), 2508–2511 (2012)
Fang, M., Peng, C.-w., Pang, D.-W., Li, Y.: Quantum dots for Cancer research: current status, remaining issues, and future perspectives. Cancer Biol. Med. 9(3), 151–163 (2012). https://doi.org/10.7497/j.issn.2095-3941.2012.03.001
Bourlinos, A.B., Bakandritsos, A., Kouloumpis, A., Gournis, D., Krysmann, M., Giannelis, E.P., Polakova, K., Safarova, K., Hola, K., Zboril, R.: Gd(iii)-doped carbon dots as a dual fluorescent-MRI probe. J. Mater. Chem. 22(44), 23327–23330 (2012). https://doi.org/10.1039/C2JM35592B
Nie, L., Wang, S., Wang, X., Rong, P., Ma, Y., Liu, G., Huang, P., Lu, G., Chen, X.: In vivo volumetric Photoacoustic molecular angiography and therapeutic monitoring with targeted plasmonic nanostars. Small. 10(8), 1585–1593 (2014). https://doi.org/10.1002/smll.201302924
Xu, M., Wang, L.V.: Photoacoustic imaging in biomedicine. Rev. Sci. Instrum. 77(4), 041101 (2006). https://doi.org/10.1063/1.2195024
Mallidi, S., Luke, G.P., Emelianov, S.: Photoacoustic imaging in cancer detection, diagnosis, and treatment guidance. Trends Biotechnol. 29(5), 213–221 (2011). https://doi.org/10.1016/j.tibtech.2011.01.006
Laufer, J., Johnson, P., Zhang, E., Treeby, B., Cox, B., Pedley, B., Beard, P.: In vivo preclinical photoacoustic imaging of tumor vasculature development and therapy. J. Biomed. Opt. 17(5), 056016 (2012). https://doi.org/10.1117/1.jbo.17.5.056016
Zhang, H.F., Maslov, K., Sivaramakrishnan, M., Stoica, G., Wang, L.V.: Imaging of hemoglobin oxygen saturation variations in single vessels in vivo using photoacoustic microscopy. Appl. Phys. Lett. 90(5), 053901 (2007). https://doi.org/10.1063/1.2435697
Wang, Z., Huang, P., Jacobson, O., Wang, Z., Liu, Y., Lin, L., Lin, J., Lu, N., Zhang, H., Tian, R., Niu, G., Liu, G., Chen, X.: Biomineralization-inspired synthesis of copper sulfide–ferritin nanocages as cancer theranostics. ACS Nano. 10(3), 3453–3460 (2016). https://doi.org/10.1021/acsnano.5b07521
McCarthy, J.R.: The future of theranostic nanoagents. Nanomedicine. 4(7), 693–695 (2009). https://doi.org/10.2217/nnm.09.58
Liang, K., Liu, F., Fan, J., Sun, D., Liu, C., Lyon, C.J., Bernard, D.W., Li, Y., Yokoi, K., Katz, M.H., Koay, E.J., Zhao, Z., Hu, Y.: Nanoplasmonic quantification of tumour-derived extracellular vesicles in plasma microsamples for diagnosis and treatment monitoring. Nat. Biomed. Eng. 1, 0021 (2017). https://doi.org/10.1038/s41551-016-0021 http://www.nature.com/articles/s41551-016-0021#supplementary-information
Maiti, S., Sen, K.K.: Bio-Targets and Drug Delivery Approaches. CRC Press LLC, Boca Raton, FL, USA (2016)
Chow, E.K.-H., Ho, D.: Cancer nanomedicine: from drug delivery to imaging. Sci. Transl. Med. 5(216), 216rv214-216rv214 (2013). https://doi.org/10.1126/scitranslmed.3005872
Acknowledgments
This work was supported by the College of Engineering and Mathematics, University of Vermont; MOST of China (Grant Nos. 2017YFA0205201, 2014CB744503, and 2013CB733802); the NSFC under Grant Nos. 81422023, 81371596, 51273165, U1705281, and U1505221; the Program for New Century Excellent Talents in University (NCET-13-0502); the Fundamental Research Funds for the Central Universities, China (20720150206 and 20720150141); and the Intramural Research Program, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health.
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Miao, T., Floreani, R.A., Liu, G., Chen, X. (2019). Nanotheranostics-Based Imaging for Cancer Treatment Monitoring. In: Rai, P., Morris, S.A. (eds) Nanotheranostics for Cancer Applications. Bioanalysis, vol 5. Springer, Cham. https://doi.org/10.1007/978-3-030-01775-0_16
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