A Comprehensive Review on Photodynamic Therapy (PDT) and Photothermal Therapy (PTT) for Cancer Treatment

A Comprehensive Review on Photodynamic Therapy (PDT) and Photothermal Therapy (PTT) for Cancer Treatment

SUMMARY Cancer is a group of diseases characterized by uncontrolled and abnormal cell growth, leading to serious health consequences. Although various approaches are available for treating cancer, including chemotherapy, surgery, radiation, and immunotherapy, the severe adverse effects of these approaches limit their clinical effectiveness. New cancer treatment strategies including phototherapy uses light to treat cancer, which has attracted wide interest in the oncology research community. There are two types of phototherapy: photodynamic therapy (PDT) and phototherapy (PTT). PDT requires the administration of a photosensitizing agent and light exposure at a particular wavelength. On the other hand, PTT uses a photothermal agent that activates and kills cancer cells at a longer wavelength of light; hence, it is less energetic and, therefore, less harmful to other cells and tissues. PTT is gaining tremendous popularity because of its limited side-effects. A significant downside of PDT is that the photosensitizing drug stays in the body for a long time, which renders the patients extremely sensitive to light exposure. PDT is useful for the treatment of lining organs as they are can be easily reached by the light source. Although PDT is helpful for treating lining organs, its potential side-effects have been reported in the treatment of skin mouth esophagus and lung cancer, among others. Therefore, PTT remains a good alternative for cancer treatment.

___

  • 1. Misra R, Acharya S, Sahoo SK. Cancer nanotechnology: application of nanotechnology in cancer therapy. Drug Discov Today 2010;15(19-20):842–50.
  • 2. Areeckal AS, Kocher M. Current and emerging diagnostic imaging-based techniques for assessment of osteoporosis and fracture risk. IEEE Rev Biomed Eng 2018;12:254–68.
  • 3. Wang X, Wang Y, Chen ZG, Shin DM. Advances of cancer therapy by nanotechnology. Cancer Res Treat 2009;41(1):1–11.
  • 4. Zou L, Wang H, He B, Zeng L, Tan T, Cao H, et al. Current approaches of photothermal therapy in treating cancer metastasis with nanotherapeutics. Theranostics 2016;6(6):762–72.
  • 5. Gomer CJ, Razum NJ. Acute skin response in albino mice following porphyrin photosensitization under oxic and anoxic conditions. Photochem Photobiol 1984;40(4):435–9.
  • 6. Chin L, Tam A, Pomerantz J, Wong M, Holash J, Bardeesy N, et al. Essential role for oncogenic Ras in tumour maintenance. Nature 1999;400(6743):468–72.
  • 7. Felsher DW, Bishop JM. Reversible tumorigenesis by MYC in hematopoietic lineages. Mol Cell 1999;4(2):199–207.
  • 8. Jain M, Arvanitis C, Chu K, Dewey W, Leonhardt E, Trinh M, et al. Sustained loss of a neoplastic phenotype by brief inactivation of MYC. Science 2002;297(5578):102–4.
  • 9. Pelengaris S, Littlewood T, Khan M, Elia G, Evan G. Reversible activation of c-Myc in skin: induction of a complex neoplastic phenotype by a single oncogenic lesion. Mol Cell 1999;3(5):565–77.
  • 10.Allison RR, Sibata CH. Oncologic photodynamic therapy photosensitizers: a clinical review. Photodiagn Photodyn 2010;7(2):61–75.
  • 11.Chen B, Roskams T, de Witte PA. Antivascular Tumor Eradication by Hypericin‐mediated Photodynamic Therapy¶. Photochem Photobiol 2002;76(5):509–13.
  • 12.Garg AD, Nowis D, Golab J, Vandenabeele P, Krysko DV, Agostinis P. Immunogenic cell death, DAMPs and anti-cancer therapeutics: an emerging amalgamation. BBA-Rev Cancer 2010;1805(1):53–71.
  • 13.De Rosa FS, Bentley MV. Photodynamic therapy of skin cancers: sensitizers, clinical studies and future directives. Pharm Res 2000;17(12):1447–55.
  • 14.Moan J, Berg K. The photodegradation of porphyrins in cells can be used to estimate the lifetime of singlet oxygen. Photochem Photobiol 1991;53(4):549–53.
  • 15.Dougherty TJ, Gomer CJ, Henderson BW, Jori G, Kessel D, Korbelik M, et al. Photodynamic therapy. J Natl Cancer Inst 1998;90(12):889–905.
  • 16.Dolmans DE, Fukumura D, Jain RK. Photodynamic therapy for cancer. Nat Rev Cancer 2003;3(5):380–7.
  • 17.Meyer-Betz F. Untersuchungen über die biologische (photodynamische) Wirkung des Hämatoporphyrins und anderer Derivate des Blut-und Gallenfarbstoffs. Dtsch Arch Für Klin Med 1913;112:476–503.
  • 18.Dougherty TJ, Grindey GB, Fiel R, Weishaupt KR, Boyle DG. Photoradiation therapy. II. Cure of animal tumors with hematoporphyrin and light. J Natl Cancer Inst 1975;55(1):115–21.
  • 19.Kelly JF, Snell ME, Berenbaum MC. Photodynamic destruction of human bladder carcinoma. Br J Cancer 1975;31(2):237–44.
  • 20.Kelly JF, Snell ME. Hematoporphyrin derivative: a possible aid in the diagnosis and therapy of carcinoma of the bladder. J Urol 1976;115(2):150–1.
  • 21.McCaughan Jr JS, Hicks W, Laufman L, May E, Roach R. Palliation of esophageal malignancy with photoradiation therapy. Cancer 1984;54(12):2905–10.
  • 22.Balchum OJ, Doiron DR, Huth GC. Photoradiation therapy of endobronchial lung cancers employing the photodynamic action of hematoporphvrin derivative. Lasers Surg Med 1984;4(1):13–30.
  • 23.Hayata Y, Kato H, Okitsu H, Kawaguchi M, Konaka C. Photodynamic therapy with hematoporphyrin derivative in cancer of the upper gastrointestinal tract. Semin Surg Oncol 1985;1(1):1–11.
  • 24.Dos Santos AF, De Almeida DR, Terra LF, Baptista MS, Labriola L. Photodynamic therapy in cancer treatment-an update review. J Cancer Metastasis Treat 2019;5(25):1–20.
  • 25.Okuno T, Kato S, Hatakeyama Y, Okajima J, Maruyama S, Sakamoto M, et al. Photothermal therapy of tumors in lymph nodes using gold nanorods and near-infrared laser light. J Control Release 2013;172(3):879–84.
  • 26.Ku G, Wang LV. Deeply penetrating photoacoustic tomography in biological tissues enhanced with an optical contrast agent. Opt Lett 2005;30(5):507–9.
  • 27.Liang C, Song X, Chen Q, Liu T, Song G, Peng R, et al. Magnetic field‐enhanced photothermal ablation of tumor sentinel lymph nodes to inhibit cancer metastasis. Small 2015;11(37):4856–63.
  • 28.Henderson TA, Morries LD. Near-infrared photonic energy penetration: can infrared phototherapy effectively reach the human brain? Neuropsychiatr Dis Treat 2015;11:2191–208.
  • 29.Hudson DE, Hudson DO, Wininger JM, Richardson BD. Penetration of laser light at 808 and 980 nm in bovine tissue samples. Photomed Laser Surg 2013;31(4):163–8.
  • 30.Guo C, Yu H, Feng B, Gao W, Yan M, Zhang Z, et al. Highly efficient ablation of metastatic breast cancer using ammonium-tungsten-bronze nanocube as a novel 1064 nm- laser-driven photothermal agent. Biomaterials 2015;52:407–16.
  • 31.Wang J, Sefah K, Altman MB, Chen T, You M, Zhao Z, et al. Aptamer‐conjugated nanorods for targeted photothermal therapy of prostate cancer stem cells.ChemAsian J 2013;8(10):2417–22.
  • 32.Zhou M, Zhao J, Tian M, Song S, Zhang R, Gupta S, et al. Radio-photothermal therapy mediated by a single compartment nanoplatform depletes tumor initiating cells and reduces lung metastasis in the orthotopic 4T1 breast tumor model. Nanoscale 2015;7(46):19438–47.
  • 33.Liu R, Jing L, Peng D, Li Y, Tian J, Dai Z. Manganese (II) chelate functionalized copper sulfide nanoparticles for efficient magnetic resonance/photoacoustic dual-modal imaging guided photothermal therapy. Theranostics 2015;5(10):1144–53.
  • 34.Wang S, Zhang Q, Luo XF, Li J, He H, Yang F, et al. Magnetic graphene-based nanotheranostic agent for dual-modality mapping guided photothermal therapy in regional lymph nodal metastasis of pancreatic cancer. Biomaterials 2014;35(35):9473–83.
  • 35.Lin Z, Liu Y, Ma X, Hu S, Zhang J, Wu Q, et al. Photothermal ablation of bone metastasis of breast cancer using PEGylated multi-walled carbon nanotubes. Sci Rep 2015;5:11709.
  • 36.Jing L. Hyaluronic acid modified hollow Prussian blue nanoparticles loading 10- hydroxycamptothecin for targeting thermochemotherapy of cancer. Theranostics 2016;6(1):40–53.
  • 37.Eckhardt BL, Francis PA, Parker BS, Anderson RL. Strategies for the discovery and development of therapies for metastatic breast cancer. Nat Rev Drug Discov 2012;11(6):479–97.
  • 38.Wang D, Xu Z, Yu H, Chen X, Feng B, Cui Z, et al. treatment of metastatic breast cancer by combination of chemotherapy and photothermal ablation using doxorubicin-loaded DNA wrapped gold nanorods. Biomaterials 2014;35(29):8374–84.
  • 39.Peng J, Qi T, Liao J, Chu B, Yang Q, Qu Y, et al. Mesoporous magnetic gold “nanoclusters” as theranostic carrier for chemo-photothermal co-therapy of breast cancer. Theranostics 2014;4(7):678–92.
  • 40.Yang TD, Choi W, Yoon TH, Lee KJ, Lee JS, Han SH, et al. Real-time phase-contrast imaging of photothermal treatment of head and neck squamous cell carcinoma: an in vitro study of macrophages as a vector for the delivery of gold nanoshells. J Biomed Opt 2012;17(12):128003.
  • 41.Kim HS, Lee DY. Near-infrared-responsive cancer photothermal and photodynamic therapy using gold nanoparticles. Polymers 2018;10(9):961.
  • 42.Turkevich J, Stevenson PC, Hillier J. A study of the nucleation and growth processes in the synthesis of colloidal gold. Discuss Faraday Soc 1951;11:55–75.
  • 43.Pitsillides CM, Joe EK, Wei X, Anderson RR, Lin CP. Selective cell targeting with light- absorbing microparticles and nanoparticles. Biophys J 2003;84(6):4023– 32.
  • 44.Martin CR. Nanomaterials: a membrane-based synthetic approach. Science 1994;266(5193):1961–6.
  • 45.Reetz MT, Helbig W. Size-selective synthesis of nanostructured transition metal clusters. J Am Chem Soc 1994;116(16):7401–2.
  • 46.Suzuki D, Kawaguchi H. Gold nanoparticle localization at the core surface by using thermosensitive core− shell particles as a template. Langmuir 2005;21(25):12016–24.
  • 47.Radloff C, Vaia RA, Brunton J, Bouwer GT, Ward VK. Metal nanoshell assembly on a virus bioscaffold. Nano Lett 2005;5(6):1187–91.
  • 48.Gobin AM, Lee MH, Halas NJ, James WD, Drezek RA, West JL. Near-infrared resonant nanoshells for combined optical imaging and photothermal cancer therapy. Nano Lett 2007;7(7):1929–34.
  • 49.Chen J, Saeki F, Wiley BJ, Cang H, Cobb MJ, Li ZY, et al. Gold nanocages: bioconjugation and their potential use as optical imaging contrast agents. Nano Lett 2005;5(3):473–7.
  • 50.Au L, Zheng D, Zhou F, Li ZY, Li X, Xia Y. A quantitative study on the photothermal effect of immuno gold nanocages targeted to breast cancer cells. ACS nano 2008;2(8):1645–52.
Türk Onkoloji Dergisi-Cover
  • ISSN: 1300-7467
  • Başlangıç: 2015
  • Yayıncı: Ali Cangül
Sayıdaki Diğer Makaleler

Subacute Cutaneous Lupus Erythematosus: A Paraneoplastic Dermatosis in Breast Carcinoma?

Özgen ARSLAN SOLMAZ, Birol YILDIZ, Ahmet KILIÇARSLAN, Selma BAKAR DERTLİOĞLU, Pervin KARABULUT

Sarcoidosis Mimicking Mediastinal Lymph Node Metastases of Cervix Carcinoma: An Unusual Association

Yassir BENAMUR, Salah Nabih OUERİAGLİ, Omar AIT SAHEL, Abderrahim DOUDOUH1

Inhibition of miR-19a-3p Increases Bortezomib-Induced Apoptosis in Myeloma Cell Lines by Targeting SOCS3

Azam KAZEMI, Saeid ABROUN, Masoud SOLEIMANI

Canine Inflammatory Mammary Carcinoma as a Promising Model for Cancer Pathology and Anticancer Drug Development: Lessons from a Case Series

Sanaz RISMANCHI, Pejman MORTAZAV, Samad MUHAMMADNEJAD

Prediction of Ipsilateral Lung Doses in Breast Radiotherapy by Anatomical Measurements Before Treatment Planning

Zümrüt Arda KAYMAK, Alper ÖZSEVEN

Nurses Attitudes Toward Cancer and Affecting Factors

Emine Derya İSTER, Yasemin ALTINBAŞ

Treatment Outcomes and Patterns of Failure in Elderly Patients with Cervical Cancer Treated with Definitive Radiotherapy

Gautam SARMA, Luri BORAH, Jyotiman NATH, Mouchumee BHATTACHARYYA, Partha Pratim MEDHI, Apurba Kumar KALITA

Active Surveillance Perspectives of Radiation Oncologists, Medical Oncologists and Urologists in the Treatment of Prostate Cancer

Ali ALKAN, İlker AKARKEN, Hayrettin ŞAHİN, Özgür TANRIVERDİ, Görkem TÜRKKAN

Apatinib Sensitizes Human Breast Cancer Cells against Navitoclax and Venetoclax Despite Up-regulated Bcl-2 and Mcl-1 Gene Expressions

Berna KAVAKCIOĞLU YARDIMCI, Özden ÖZGÜN ACAR, Aslı SEMİZ, Alaattin ŞEN4

Communication Skills between the Relatives and the Doctors of Patients with Cancer Treated in Radiation Oncology: A Cross-sectional Questionnaire Study

İlknur ALSAN ÇETİN, Sıtkı Utku AKAY, Mehmet Faruk UÇUM, Ahmet Raşit NOHUT, Muhammed İkbal KAYA, İbrahim Kara, Ahmet Abdurrahman Ulu