Semiconductor Nanomaterials for Radiotherapy, Radiotherapy Combined with Nano-Biomaterials and Various Approaches to Enhance Radiosensitization in Cancer
Keywords:
Radiotherapy, Nano-biomaterials, Radio-sensitization, CancerAbstract
Radiotherapy often fails and tumours recur after treatment because of acquired radiation resistance. To improve the safety and effectiveness of radiation therapy while reducing radiation resistance, many methods have been employed. Radiation therapy has been greatly improved in three main ways: (I) by making tumour tissue more radio-sensitized; (II) by making tumour tissue less resistant to radiation; and (III) by making healthy tissue more radio-resistant. Because of their dual role as a treatment and a carrier for other medicines, nanoparticles have been essential in improving radiation therapy. We summarise the current studies on improved radio-sensitization in cancer utilising several species of nanoparticles in this review. Because it is both noninvasive and highly adaptable, radiation therapy (RT) is a crucial component of tumour treatment. Scientists and physicians alike are understandably worried about the newfound ability of radiation therapy to trigger an immune response that fights tumours. This review focuses on the most up-to-date research on radiotherapy-activated immunotherapy using nano-biomaterials. To improve the efficacy of radiotherapy and promote the tumour immune response, we first explore the combination of several radio sensitising nano-biomaterials with immune checkpoint inhibitors. Afterwards, different tumour oxygenation techniques that utilise nano-biomaterials are implemented to improve the hypoxic tumour environment and enhance the immunomodulatory effect. Radiotherapy revitalises the immune system of the host by means of adjuvants and nano-vaccines. There is an increase in anti-tumor immunity mediated by the innate immune system when using nano-biomaterials that are responsive to ionising radiation. Lastly, we review the state of the art in immune modulatable nano-biomaterials and address the main obstacle to their further development for tumour radio-immunotherapy. Clinical radiotherapy and immunotherapy can be optimised and new combinational therapeutic modalities developed with an understanding of nano-biomaterials-assisted radio-immunotherapy.
Downloads
References
Jeremic B, Aguerri AR, Filipovic N. Radiosensitization by gold nanoparticles. Clin Transl Oncol 2013;15:593-601.
Larson TA, Joshi PP, Sokolov K. Preventing protein adsorption and macrophage uptake of gold nanoparticles via a hydrophobic shield. ACS Nano 2012;6:9182-90.
Wang M, Thanou M. Targeting nanoparticles to cancer. Pharmacol Res 2010;62:90-9. 13. Zheng Y, Hunting DJ, Ayotte P, et al. Radiosensitization of DNA by gold nanoparticles irradiated with high-energy electrons. Radiat Res 2008;169:19-27.
Brun E, Sanche L, Sicard-Roselli C. Parameters governing gold nanoparticle X-ray radiosensitization of DNA in solution. Colloids Surf B Biointerfaces 2009;72:128-34. 15. Lechtman E, Chattopadhyay N, Cai Z, et al. Implications on clinical scenario of gold nanoparticle radiosensitization in regards to photon energy, nanoparticle size, concentration and location. Phys Med Biol 2011;56:4631-47.
McMahon SJ, Prise KM, Currell FJ. Comment on ‘implications on clinical scenario of gold nanoparticle radiosensitization in regard to photon energy, nanoparticle size, concentration and location’. Phys Med Biol 2012;57:287-90; discussion 291-5.
Ngwa W, Korideck H, Kassis AI, et al. In vitro radiosensitization by gold nanoparticles during continuous low-dose-rate gamma irradiation with I-125 brachytherapy seeds. Nanomedicine 2013;9:25-7.
Alqathami M, Blencowe A, Yeo UJ, et al. Novel multicompartment 3-dimensional radiochromic radiation dosimeters for nanoparticle-enhanced radiation therapy dosimetry. Int J Radiat Oncol Biol Phys 2012;84:e549-55.
Joh DY, Sun L, Stangl M, et al. Selective targeting of brain tumors with gold nanoparticle-induced radiosensitization. PLoS One 2013;8:e62425.
Bobyk L, Edouard M, Deman P, et al. Photoactivation of gold nanoparticles for glioma treatment. Nanomedicine 2013. [Epub ahead of print].
Xiao F, Zheng Y, Cloutier P, et al. On the role of lowenergy electrons in the radiosensitization of DNA by gold nanoparticles. Nanotechnology 2011;22:465101.
Liu CJ, Wang CH, Chien CC, et al. Enhanced x-ray irradiation-induced cancer cell damage by gold nanoparticles treated by a new synthesis method of polyethylene glycol modification. Nanotechnology 2008 Jul;19:295104.
Liu CJ, Wang CH, Chen ST, et al. Enhancement of cell radiation sensitivity by pegylated gold nanoparticles. Phys Med Biol 2010;55:931-45.
Zhang XD, Wu D, Shen X, et al. Size-dependent radiosensitization of PEG-coated gold nanoparticles for cancer radiation therapy. Biomaterials 2012;33:6408-19.
Cho WS, Kim S, Han BS, et al. Comparison of gene expression profiles in mice liver following intravenous injection of 4 and 100 nm-sized PEG-coated gold nanoparticles. Toxicol Lett 2009;191:96-102.
Zhang XD, Wu D, Shen X, et al. Size-dependent in vivo toxicity of PEG-coated gold nanoparticles. Int J Nanomedicine 2011;6:2071-81. 27. Coulter JA, Jain S, Butterworth KT, et al. Cell typedependent uptake, localization, and cytotoxicity of 1.9 nm gold nanoparticles. Int J Nanomedicine 2012;7:2673-85. 28. Zhang XD, Wu HY, Wu D, et al. Toxicologic effects of gold nanoparticles in vivo by different administration routes. Int J Nanomedicine 2010;5:771-81. 29. Jeong SY, Park SJ, Yoon SM, et al. Systemic delivery and preclinical evaluation of Au nanoparticle containing beta-lapachone for radiosensitization. J Control Release 2009;139:239-45.
Schaue D, McBride WH. Opportunities and challenges of radiotherapy for treating cancer. Nat Rev Clin Oncol. 2015;12:527–40.
Prise KM, O’Sullivan JM. Radiation-induced bystander signalling in cancer therapy. Nat Rev Cancer. 2009;9:351–60. 6. Mole RH. Whole body irradiation; radiobiology or medicine? Br J Radiol. 1953;26:234–41.
Lee Y, Auh SL, Wang Y, Burnette B, Wang Y, Meng Y, Beckett M, Sharma R, Chin R, Tu T, et al. Therapeutic efects of ablative radiation on local tumor require CD8+ T cells: changing strategies for cancer treatment. Blood. 2009;114:589–95.
Demaria S, Golden EB, Formenti SC. Role of local radiation therapy in cancer immunotherapy. JAMA Oncol. 2015;1:1325–32.
Postow MA, Callahan MK, Barker CA, Yamada Y, Yuan J, Kitano S, Mu Z, Rasalan T, Adamow M, Ritter E, et al. Immunologic correlates of the abscopal efect in a patient with melanoma. N Engl J Med. 2012;366:925–31.
Demaria S, Kawashima N, Yang AM, Devitt ML, Babb JS, Allison JP, Formenti SC. Immune-mediated inhibition of metastases after treatment with local radiation and CTLA-4 blockade in a mouse model of breast cancer. Clin Cancer Res. 2005;11:728–34.
Dewan MZ, Galloway AE, Kawashima N, Dewyngaert JK, Babb JS, Formenti SC, Demaria S. Fractionated but not single-dose radiotherapy induces an immune-mediated abscopal efect when combined with anti-CTLA-4 antibody. Clin Cancer Res. 2009;15:5379–88.
Twyman-Saint Victor C, Rech AJ, Maity A, Rengan R, Pauken KE, Stelekati E, Benci JL, Xu B, Dada H, Odorizzi PM, et al. Radiation and dual checkpoint blockade activate non-redundant immune mechanisms in cancer. Nature. 2015;520:373–7.
Tang C, Welsh JW, de Groot P, Massarelli E, Chang JY, Hess KR, Basu S, Curran MA, Cabanillas ME, Subbiah V, et al. Ipilimumab with stereotactic ablative radiation therapy: phase I results and immunologic correlates from peripheral T cells. Clin Cancer Res. 2017;23:1388–96.
Hiniker SM, Reddy SA, Maecker HT, Subrahmanyam PB, RosenbergHasson Y, Swetter SM, Saha S, Shura L, Knox SJ. A prospective clinical trial combining radiation therapy with systemic immunotherapy in metastatic melanoma. Int J Radiat Oncol Biol Phys. 2016;96:578–88.
Kieran MW, Goumnerova L, Manley P, Chi SN, Marcus KJ, Manzanera AG, Polanco MLS, Guzik BW, Aguilar-Cordova E, Diaz-Montero CM, et al. Phase I study of gene-mediated cytotoxic immunotherapy with AdV-tk as adjuvant to surgery and radiation for pediatric malignant glioma and recurrent ependymoma. Neuro Oncol. 2019;21:537–46.
Yuan Z, Fernandez D, Dhillon J, Abraham-Miranda J, Awasthi S, Kim Y, Zhang J, Jain R, Serna A, Pow-Sang JM, et al. Proof-of-principle Phase I results of combining nivolumab with brachytherapy and external beam radiation therapy for Grade Group 5 prostate cancer: safety, feasibility, and exploratory analysis. Prostate Cancer Prostatic Dis. 2020;24:140–9.
Koller KM, Mackley HB, Liu J, Wagner H, Talamo G, Schell TD, Pameijer C, Neves RI, Anderson B, Kokolus KM, et al. Improved survival and complete response rates in patients with advanced melanoma treated with concurrent ipilimumab and radiotherapy versus ipilimumab alone. Cancer Biol Ther. 2017;18:36–42.
Abei M, Okumura T, Fukuda K, Hashimoto T, Araki M, Ishige K, Hyodo I, Kanemoto A, Numajiri H, Mizumoto M, Sakae T, et al. A phase I study on combined therapy with proton-beam radiotherapy and in situ tumor vaccination for locally advanced recurrent hepatocellular carcinoma. Radiat Oncol. 2013;16:239.
Chen Q, Chen M, Liu Z. Local biomaterials-assisted cancer immunotherapy to trigger systemic antitumor responses. Chem Soc Rev. 2019;48:5506–26.
Pei P, Shen W, Zhou H, Sun Y, Zhong J, Liu T, Yang K. Radionuclide labeled gold nanoclusters boost efective anti-tumor immunity for augmented radio-immunotherapy of cancer. Nano Today. 2021;38: 101144.
Ni KY, Lan GX, Song Y, Hao ZY, Lin WB. Biomimetic nanoscale metalorganic framework harnesses hypoxia for efective cancer radiotherapy and immunotherapy. Chem Sci. 2020;11:7641–53.
Pei P, Shen W, Zhang Y, Zhang Y, Qi Z, Zhou H, Liu T, Sun L, Yang K. Radioactive nano-oxygen generator enhance anti-tumor radioimmunotherapy by regulating tumor microenvironment and reducing proliferation. Biomaterials. 2022;280: 121326.
Pan P, Dong X, Chen Y, Ye JJ, Sun YX, Zhang XZ. A heterogenic membranebased biomimetic hybrid nanoplatform for combining radiotherapy and immunotherapy against breast cancer. Biomaterials. 2022;289: 121810.
Yu H, Yang Y, Jiang TY, Zhang XH, Zhao YH, Pang GB, Feng YH, Zhang SL, Wang FJ, Wang Y, et al. Efective radiotherapy in tumor assisted by Ganoderma lucidum polysaccharide-conjugated bismuth sulfde nanoparticles through radiosensitization and dendritic cell activation. ACS Appl Mater Interfaces. 2019;11:27536–47.
Gong F, Chen MC, Yang NL, Dong ZL, Tian LL, Hao Y, Zhuo MP, Liu Z, Chen Q, Cheng L. Bimetallic oxide FeWO(X)Nanosheets as multifunctional cascade bioreactors for tumor microenvironment-modulation and enhanced multimodal cancer therapy. Adv Funct Mater. 2020;30:2002753.
Lu K, He C, Guo N, Chan C, Ni K, Lan G, Tang H, Pelizzari C, Fu Y, Spiotto M, et al. Low-dose X-ray radiotherapy-radiodynamic therapy via nanoscale metal-organic frameworks enhances checkpoint blockade immunotherapy. Nat Biomed Eng. 2018;2:600–10.
Allison, R. R., G. H. Downie et al. 2004. Photosensitizer in clinical PDT. Photodiagnosis and Photodynamic Therapy 1:27. Andrews, D. L. 1989. A unified theory of radiative and radiationless molecular-energy transfer. Chemical Physics 135(2):195–201.
Bawendi, M. G., M. L. Steigerwald et al. 1990. The quantum- mechanics of larger semiconductor clusters (quantum dots). Annual Review of Physical Chemistry 41:477–496.
Beaulac, R., L. Schneider et al. 2009. Light-induced spontaneous magnetization in doped colloidal quantum dots. Science 325(5943):973–976.
Biju, V., T. Itoh et al. 2006. Quenching of photoluminescence in conjugates of quantum dots and single-walled carbon nanotube. Journal of Physical Chemistry B 110(51):26068–26074.
Cameron, J. R., M. G. Ort et al. 1969. A TLD measurement of x-ray quality and output simultaneously. Physics in Medicine and Biology 14(2):338.
Cervino, L. I., J. Du et al. 2011. MRI-guided tumor tracking in lung cancer radiotherapy. Physics in Medicine and Biology 56(13):3773–3785.
Chen, W., J. O. Malm et al. 2000. Energy structure and fluorescence of Eu2+ in ZnS:Eu nanoparticles. Physical Review B 61(16):11021–11024.
Colon, J., L. Herrera et al. 2009. Protection from radiation- induced pneumonitis using cerium oxide nanoparticles. Nanomedicine 5(2):225–231.
D’Souza, W. D., and Rosen, I. I. 2003. Nontumor integral dose variation in conventional radiotherapy treatment planning. Medical Physics 30(8):2065–2071.
Eberhardt, W., C. Pottgen et al. 2006. Chemoradiation paradigm for the treatment of lung cancer. Nature Clinical Practice Oncology 3(4):188–199.
Farrell, T. J., B. C. Wilson et al. 1998. Comparison of the in vivo photodynamic threshold dose for photofrin, mono- and tetrasulfonated aluminum phthalocyanine using a rat liver model. Photochemistry and Photobiology 68(3):394–399.
Gladstone, D. J., X. Q. Lu et al. 1994. A miniature mosfet radiation dosimeter probe. Medical Physics 21(11):1721–1728.
Raaymakers, B. W., J. C. de Boer et al. 2011. Integrated mega- voltage portal imaging with a 1.5 T MRI linac. Physics in Medicine and Biology 56(19):N207–N214.
Regulla, D. F., L. B. Hieber et al. 1998. Physical and biological interface dose effects in tissue due to X-ray-induced release of secondary radiation from metallic gold surfaces. Radiation Research 150(1):92–100.
Rose, J. H., A. Norman et al. 1999. First radiotherapy of human metastatic brain tumors delivered by a computerized tomography scanner (CTRx). International Journal of Radiation Oncology Biology Physics 45(5):1127–1132.
Sahare, P. D., R. Ranjan et al. 2007. K3Na(SO4)(2): Eu nanoparticles for high dose of ionizing radiation. Journal of Physics D Applied Physics 40(3):759–764. Salah, N., P. D. Sahare et al. 2006. TL and PL studies on CaSO4: Dy nanoparticles. Radiation Measurements 41(1):40–47. #
Wilson, B. C. and M. S. Patterson. 2008. The physics, biophysics and technology of photodynamic therapy. Phys Med Biol 53(9):R61–109.
Yang, W., P. W. Read et al. 2007. Novel FRET-based radio- sensitization using quantum dot–photosensitizer conjugates. Signals, Systems and Computers ACSSC 2007:1861–1865.
Yang, W., P. W. Read et al. 2008. Semiconductor nanoparticles as energy mediators for photosensitizer-enhanced radio- therapy. International Journal of Radiation Oncology Biology Physics 72(3):633–635.
Zelefsky, M. J., Y. Yamada et al. 2008. Long-term results of con- formal radiotherapy for prostate cancer: Impact of dose escalation on biochemical tumor control and distant metastases-free survival outcomes. International Journal of Radiation Oncology Biology Physics 71(4):1028–1033.

Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2024 Clinical Images and Case Reports

This work is licensed under a Creative Commons Attribution 4.0 International License.
Clinical Images and Case Reports