5 курс / Пульмонология и фтизиатрия / Лазерная_терапия_в_онкологии_Москвин_С_В_,_Стражев

Лазерная терапия в онкологии

2241. Saygun I., Karacay S., Serdar M. et al. Effects of laser irradiation on the release of basic fibroblast growth factor (bFGF), insulin like growth factor-1 (IGF-1), and receptor of IGF-1 (IGFBP3) from gingival fibroblasts // Lasers in Medical Science. – 2008, 23 (2): 211–215. doi: 10.1007/s10103-007-0477-3.

2242. Schaffer M., Bonel H., Sroka R. et al. Effects of 780 nm diode laser irradiation on blood microcirculation: preliminary findings on time-dependent T1-weighted contrast-enhanced magnetic resonance imaging (MRI) // J. Photochem. Photobiol. B: Biol. – 2000, 54 (1): 55–60.

2243. Schaffer M., Bonel H., Sroka R. et al. Magnetic resonance imaging (MRI) controlled outcome of side effects caused by ionizing radiation, treated with 780 nm-diode laser – preliminary results // J. Photochem. Photobiol. B: Biol. – 2000(1), 59 (1–3): 1–8.

2244. Schaffer M., Sroka R., Fuchs C. et al. Biomodulative effects induced by 805 nm laser light irradiation of normal and tumor cells // J. Photochem. Photobiol. B. – 1997, 40 (3): 253–257.

2245. Schalch T.D., Fernandes M.H., Destro Rodrigues M.F.S. et al. Photobiomodulation is associated with a decrease in cell viability and migration in oral squamous cell carcinoma // Lasers in Medical Science. – 2019, 34 (3): 629–636. doi: 10.1007/s10103-018-2640-4.

2246. Schartinger V.H., Galvan O., Riechelmann H., Dudás J. Differential responses of fibroblasts, non-neoplas- tic epithelial cells, and oral carcinoma cells to low-level laser therapy // Support Care Cancer. – 2012, 20 (3): 523–529. doi: 10.1007/s00520-011-1113-0.

2247. Schiffer F., Johnston A.L., Ravichandran C. et al. Psychological benefits 2 and 4 weeks after a single treatment with near infrared light to the forehead: a pilot study of 10 patients with major depression and anxiety // Behav. Brain Funct. – 2009, 5: 46.

2248. Schindl A., Neumann R. Low-intensity laser therapy is an effective treatment for recurrent herpes simplex infection. Results from a randomized double-blind placebo-controlled study // J. Invest. Dermatol. – 1999, 113 (2): 221–223. doi: 10.1046/j.1523-1747.1999.00684.x.

2249. Schook C.C., Mulliken J.B., Fishman S.J. et al. Primary lymphedema: clinical features and management in 138pediatricpatients//Plast.Reconstr.Surg.–2011,127(6):2419–2431.doi:10.1097/PRS.0b013e318213a218. 2250. Schubert M.M., Eduardo F.P., Guthrie K.A. et al. A phase III randomized placebo-controlled clinical trial to determine the efficacy of low level laser therapy for the prevention of oral mucositis in patients undergoing hematopoietic cell transplantation // Support Care Cancer. – 2007, 15: 1145–1154.

2251. Schubert M.M., Franquin J.C., Niccoli-Filho F. et al. Effects of low-energy laser on oral mucositis: a phase 1/11 pilot study // Cancer Researcher Weekly. – 1994, 7: 14.

2252. Schwartz M., Doron A., Erlich M. et al. Effects of low-energy He-Ne laser irradiation on posttraumatic degeneration of adult rabbit optic nerve // Lasers in Surgery and Medicine. – 1987, 7 (1): 51–55.

2253. Scoletta M., Arduino P.G., Reggio L. et al. Effect of low-level laser irradiation on bisphosphonate-induced osteonecrosis of the jaws: preliminary results of a prospective study // Photomedicine and Laser Surgery. – 2010, 28 (2): 179–184. doi: 10.1089/pho.2009.2501.

2254. Sekhejane P.R., Manoto S.L., Houreld N.N., Abrahamse H. Phototoxic effect of zinc sulphophthalocyanine photosensitizer on human colon (Dld-1) and lung (A549) carcinoma cells (in vitro) // Conference WALT. Abstracts. – Bergen, Norway, 2010. – P. 109.

2255. Sergio L.P., Marciano R. da S., Teixeira G.R. et al. Therapeutic low-intensity red laser for herpes labialis on plasmid survival and bacterial transformation // Photochem. Photobiol. Sci. – 2013, 12 (5): 930–935. doi: 10.1039/c3pp25394e.

2256. Shankar A., Roy S., Bhandari M. et al. Current trends in management of oral mucositis in cancer treatment //Asian Pac. J. Cancer. Prev. – 2019, 18 (8): 2019–2026. doi: 10.22034/APJCP.2017.18.8.2019.

2257. Shaw V.E., Spana S., Ashkan K. et al. Neuroprotection of midbrain dopaminergic cells in MPTP-treated mice after near-infrared light treatment // J. Comp. Neurol. – 2010, 518 (1): 25–40.

2258. Sheiko E.A., ShikhlyarovaA.I., Maryanovskaya G.Ia. et al. Experimental study of the effects of low-intensi- ty monochromatic photodiode radiation and antitumor efficiency of cyclophosphamide injected with autoblood // Bulletin of Experimental Biology and Medicine. – 2011, 151 (1): 58–61.

2259. Shen J., Wenger N., Glaspy J. et al. Electroacupuncture for control of myeloblative chemo-therapy-induced emesis: a randomized controlled trial // JAMA. – 2000, 284 (21): 2755–2761.

2260. Shinohara S., Kobayashi K., Kasahara C. et al. Long-term impact of complications after lung resections in non-small cell lung cancer // J. Thorac. Dis. – 2019, 11 (5): 2024–2033. doi: 10.21037/jtd.2019.04.91.

2261. Silva G.B., Mendonça E.F., Bariani C. et al. The prevention of induced oral mucositis with low-level laser therapyin bonemarrow transplantationpatients:arandomizedclinicaltrial // PhotomedicineandLaserSurgery. – 2011, 29 (1): 27–31. doi: 10.1089/pho.2009.2699.

2262. Silva G.B., Sacono N.T., Othon-Leite A.F. et al. Effect of low-level laser therapy on inflammatory mediator release during chemotherapy-induced oral mucositis: a randomized preliminary study // Lasers in Medical Science. – 2015, 30 (1): 117–126. doi: 10.1007/s10103-014-1624-2.

950

Список литературы

2263. Silva L.C., Sacono N.T., Freire M.do C. et al. The impact of low-level laser therapy on oral mucositis and quality of life in patients undergoing hematopoietic stem cell transplantation using the oral health impact profile and the functional assessment of cancer therapy-bone marrow transplantation questionnaires // Photomedicine and Laser Surgery. – 2015(1), 33 (7): 357–363. doi: 10.1089/pho.2015.3911.

2264. Silva V.R., Marcondes P., Silva M. et al. Low-level laser therapy inhibits bronchoconstriction, Th2 inflammation and airway remodeling in allergic asthma // Respir. Physiol. Neurobiol. – 2014, 194: 37–48. doi: 10.1016/j.resp.2014.01.008.

2265. Silveira F.M., Paglioni M.P., Marques M.M. et al. Examining tumor modulating effects of photobiomodulation therapy on head and neck squamous cell carcinomas // Photochemical and photobiological sciences. – 2019, 18 (7): 1621–1637. doi: 10.1039/c9pp00120d.

2266. Silveira L.B., Prates R.A., Novelli M.D. et al. Investigation of mast cells in human gingiva following low-intensity laser irradiation // Photomedicine and Laser Surgery. – 2008, 26 (4): 315–321. doi: 10.1089/ pho.2007.2140.

2267. Simões A., de Campos L., de Souza D.N. et al. Laser phototherapy as topical prophylaxis against radiationinduced xerostomia // Photomedicine and Laser Surgery. – 2010, 28 (3): 357–363. doi: 10.1089/pho.2009.2486. 2268. Simões A., de Paula Eduardo F., Migliorati C.A., Schubert M.M. Low level laser therapy in the prevention and treatment of oral mucositis // Lasers in dentistry: guide for clinical practice / P.M. de Freitas, A. Simões (Eds.). –Ames (USA), West Sussex, Oxford (UK): Blackwell Publishing, 2015. – P. 321–330.

2269. Simões A., Eduardo F.P., Luiz A.C. et al. Laser phototherapy as topical prophylaxis against head and neck cancer radiotherapy-induced oral mucositis: comparison between low and high/low power lasers // Lasers in Surgery and Medicine. – 2009, 41 (4): 264–270. doi: 10.1002/lsm.20758.

2270. SimõesA., Nicolau J., de Souza D.N. et al. Effect of defocused infrared diode laser on salivary flow rate and some salivary parameters of rats // Clin. Oral Investig. – 2008, 12 (1): 25–30. doi: 10.1007/s00784-007-0135-y. 2271. Simões A., Platero M.D., Campos L. et al. Laser as a therapy for dry mouth symptoms in a patient with Sjögren’s syndrome: a case report // Spec. Care Dentist. – 2009(1), 29 (3): 134–137. doi: 10.1111/j.17544505.2009.00078.x.

2272. Simões A., Siqueira W.L., Lamers M.L. et al. Laser phototherapy effect on protein metabolism parameters of rat salivary glands // Lasers in Medical Science. – 2009(2), 24 (2): 202–208. doi: 10.1007/s10103-008-0548-0. 2273. Simunović-Soskić M., Pezelj-Ribarić S., Brumini G. et al. Salivary levels of TNF-alpha and IL-6 in patients with denture stomatitis before and after laser phototherapy // Photomedicine and Laser Surgery. – 2010, 28 (2): 189–193. doi: 10.1089/pho.2008.2420.

2274. Singh H.M.P., Bajpai A., Bisarya B.N., Bhargava K.D. Low level laser therapy (LLLT) with nitrogen and helium neon lasers in multiple drug resistant pulmonary tuberculosis: a preliminary study // Laser Therapy. – 1997, 9 (4): 173–179.

2275. Singh J.P., Babcock D.F., Lardy H.A. Motility activation, respiratory stimulation, and alteration of Ca2+ transport in bovine sperm treated with amine local anesthetics and calcium transport antagonists // Arch. Biochem. Biophys. – 1983, 221 (1): 291–303.

2276. Skobelkin O.K., Michailov V.A., Zakharov S.D. Preoperative activation of the immune system by low reactive level laser therapy (LLLT) in oncologic patients: a preliminary report // LaserTherapy. – 1991, 3 (4): 169–175. 2277. Sliney D.H., Wolbarsht M.L. Safety with lasers and other optical radiation sources. – New York: Plenum Press, 1980. – 1035 p.

2278. Smalley P.J. Laser safety: risks, hazards and control measures // Laser Therapy. – 2011, 20 (2): 95–106. 2279. Smith B.G., Lewin J.S. Lymphedemamanagementinheadandneckcancer // Curr.Opin.Otolaryngol.Head Neck Surg. – 2010, 18 (3): 153–158. doi: 10.1097/MOO.0b013e32833aac21.

2280. Smith K.C. Light and life: photobiological basis of the therapeutic use of radiation from lasers, in: Selected papers from the October 1990 ILTA Congress «Progress in laser therapy». – Chichester, England: John Wiley & Sons, 1990. – P. 11–18.

2281. Smoot B., Chiavola-Larson L., Lee J. et al. Effect of low-level laser therapy on pain and swelling in women with breast cancer-related lymphedema: a systematic review and meta-analysis // J. Cancer. Surviv. – 2015, 9 (2): 287–304. doi: 10.1007/s11764-014-0411-1.

2282. Soares R.G., Farias L.C., da Silva Menezes A.S. et al. Treatment of mucositis with combined 660and 808-nm-wavelength low-level laser therapy reduced mucositis grade, pain, and use of analgesics: a parallel, single-blind, two-arm controlled study // Lasers in Medical Science. – 2018, 33 (8): 1813–1819. doi: 10.1007/ s10103-018-2549-y.

2283. Sommer A.P., Scharnweber T. Extraordinary anticancer effect of green tea and red light // Photomedicine and Laser Surgery. – 2010, 28 (3): 429–430. doi: 10.1089/pho.2009.2706.

2284. Sonis S.T. Mucositis: the impact, biology and therapeutic opportunities of oral mucositis // Oral Oncol. – 2009, 45 (12): 1015–1020. doi: 10.1016/j.oraloncology.2009.08.006.

951

Рекомендовано к покупке и изучению сайтом МедУнивер - https://meduniver.com/

Лазерная терапия в онкологии

2285. Sonis S.T. The biologic role for nuclear factor-kappa B in disease and its potential involvement in mucosal injury associated with anti-neoplasic therapy // Crit. Rev. Oral Biol. Med. – 2002, 13 (5): 380–389. PMID: 12393757.

2286. Sonis S.T. Thepathobiologyofmucositis//Nat.Rev.Cancer.–2004,4(4):277–284.doi:10.1038/nrc1318. 2287. Sonis S.T., Elting L.S., Keefe D. et al. Perspectivesoncancertherapy-inducedmucosalinjury:pathogenesis, measurement, epidemiology, and consequences for patients // Cancer. – 2004, 100 (9 Suppl): 1995–2025. doi: 10.1002/cncr.20162.

2288. Sonis S.T., Hashemi S., Epstein J.B. et al. Could the biological robustness of low level laser therapy (photobiomodulation) impact its use in the management of mucositis in head and neck cancer patients // Oral Oncol. – 2016, 54: 7–14. doi: 10.1016/j.oraloncology.2016.01.005.

2289. Soto M., Lalla R.V., Gouveia R.V. et al. Pilot study on the efficacy of combined intraoral and extraoral low-level laser therapy for prevention of oral mucositis in pediatric patients undergoing hematopoietic stem cell transplantation // Photomedicine and Laser Surgery. – 2015, 33 (11): 540–546. doi: 10.1089/pho.2015.3954.

2290. Sousa L.R., Cavalcanti B.N., Marques M.M. Effect of laser phototherapy on the release of TNF-α and MMP-1 by endodontic sealer–stimulated macrophages // Photomedicine and Laser Surgery. – 2009, 27 (1): 37– 42. doi: 10.1089/pho.2007.2220.

2291. Souza N.H., Marcondes P.T.,Albertini R. et al. Low-levellasertherapysuppressestheoxidativestress-indu- ced glucocorticoids resistance in U937 cells: Relevance to cytokine secretion and histone deacetylase in alveolar macrophages // J. Photochem. Photobiol. B: Biol. – 2014, 130: 327–336. doi: 10.1016/j.jphotobiol.2013.12.010. 2292. Spanemberg J.C., Zancanaro de Figueiredo M.A., Cherubini K. et al. Low-level laser therapy: a review of its applications in the management of oral mucosal disorders //Altern. Ther. Health Med. – 2016, 22 (6): 24–31. 2293. Sperandio F.F., Giudice F.S., Correa L. et al. Low-level laser therapy can produce increased aggressiveness of dysplastic and oral cancer cell lines by modulation ofAkt/mTOR signaling pathway // J. Biophotonics – 2013, 6 (10): 839–847. doi: 10.1002/jbio.201300015.

2294. Spivakovsky S. Low level laser therapy may reduce risk of oral mucositis // Evid. Based Dent. – 2015, 16 (2): 49. doi: 10.1038/sj.ebd.6401095.

2295. Stergioulas A. Low-level laser treatment can reduce edema in second degree ankle sprains // Journal of Clinical Laser Medicine & Surgery. – 2004, 22 (2): 125–128. doi: 10.1089/104454704774076181.

2296. Stockert K., Schneider B., Porenta G. et al. Laser acupuncture and probiotics in school age children with asthma: a randomized, placebo-controlled pilot study of therapy guided by principles of Traditional Chinese Medicine // Pediatr. Allergy Immunol. – 2007, 18 (2): 160–166. Erratum in: Pediatr. Allergy Immunol. – 2007, 18 (3): 272.

2297. Stona P., da Silva Viana E., Dos Santos Pires L. et al. Recurrent labial Herpes simplex in pediatric dentistry: low-level laser therapy as a treatment option // Int. J. Clin. Pediatr. Dent. – 2014, 7 (2): 140–143. doi: 10.5005/ jp-journals-10005-1252.

2298. Stone J.A.M., Johnstone P.A.S. Mechanisms of action for acupuncture in the oncology setting // Current Treatment Options in Oncology. – 2010, 11 (3–4): 118–127. doi: 10.1007/s11864-010-0128-y.

2299. Storz M.A., Gronwald B., Gottschling S. et al. Photobiomodulationtherapyinbreastcancer-relatedlymphe- dema: a randomized placebo-controlled trial // Photodermatol Photoimmunol Photomed. – 2017, 33 (1): 32–40. doi: 10.1111/phpp.12284.

2300. Stout N.L., Pfalzer L.A., Springer B. et al. Breast cancer-related lymphedema: comparing direct costs of a prospective surveillance model and a traditional model of care // Phys. Ther. – 2012, 92 (1): 152–163. doi: 10.2522/ptj.20100167.

2301. Szuba A., Cooke J.P., Yousuf S. et al. Decongestive lymphatic therapy for patients with cancer-related or primary lymphedema //Am. J. Med. – 2000, 109 (4): 296–300. doi: 10.1016/s0002-9343 (00)00503-9.

2302. Tadakuma T. Possible application of the laser in immunobiology // Keio J. Med. – 1993, 42 (4): 180–182. 2303. Takeda Y. Irradiation effect of low-energy laser on rat submandibular salivary gland // J. Oral Pathol. – 1988, 17 (2): 91–94. doi: 10.1111/j.1600-0714.1988.tb01513.x.

2304. Takemoto M.M., Garcez A.S., Sperandio M. High energy density LED-based photobiomodulation inhibits squamous cell carcinoma progression in co-cultures in vitro // J. Photochem. Photobiol. B. – 2019, 199: 111592. doi: 10.1016/j.jphotobiol.2019.111592.

2305. Thelander A. Laser therapy for lymphedema // J National Women’s Health Group (Australian PhysiotherapyAssoc). – 1994, 13: 26–30.

2306. Thelander A., Piller N.B. Post surgical oedema treated by low level scanning laser // Third Australasian LymphologyAssociation Conference. – 2000: 129–132.

2307. Thieme S., Ribeiro J.T., Dos Santos B.G. et al. Comparison of photobiomodulation using either an intraoral or an extraoral laser on oral mucositis induced by chemotherapy in rats // Support Care Cancer. – 2019. doi: 10.1007/s00520-019-04889-9 [Epub ahead of print].

952

Список литературы

2308. Thompson S., Chen X., Hui L. et al. Low concentrations of a non-hydrolysable tetra-S-glycosylated porphyrin and low light induces apoptosis in human breast cancer cells via stress of the endoplasmic reticulum // Photochemical & Photobiological Sciences. – 2008, 7 (11): 1415–1421. doi: 10.1039/b806536e.

2309. Tilley S. Use of laser therapy in the management of lymphoedema // Journal of Lymphoedema. – 2009, 4 (1): 39–43.

2310. Tombes R.M., Borisy G.G. Intracellular free calcium and mitosis in mammalian cells: anaphase onset is calcium modulated, but is not triggered by a brief transient // J. Cell Biol. – 1989, 109 (2): 627–636.

2311. Tong M., Liu Y.-F., Zhao X.-N. et al. Effects of different wavelengths of low level laser irradiation on murine immunological activity and intracellular Ca2+ in human lymphocytes and cultured cortical neurogliocytes // Lasers in Medical Science. – 2000, 15 (3): 201–206. doi: 10.1007/PL00011318.

2312. Torres Lacomba M., Yuste Sánchez M.J., Zapico Goñi A. et al. Effectiveness of early physiotherapy to prevent lymphoedema after surgery for breast cancer: Randomised single blinded clinical trial // BMJ. – 2010, 340: b5396. doi: 10.1136/bmj.b5396.

2313. Tracol J., Foussard-Blanpin O., Zoute J., Lesage G. Etiopathology and treatment of oral aphthae // Chir. Dent. Fr. – 1991, 61 (565): 49–58. [Article in French].

2314. Trautinger F. Lasers in medicine // Photochemical and photobiological sciences. – 2019, 18 (7): 1619– 1620. doi: 10.1039/C9PP90031D.

2315. Trotti A., Bellm L.A., Epstein J.B. et al. Mucositis incidence, severity and associated outcomes in patients with head and neck cancer receiving radiotherapy with or without chemotherapy: a systematic literature review // Radiother. Oncol. – 2003, 66 (3): 253–262.

2316. Tsien R.Y., Poenie M. Fluorescenceratioimaging:anewwindowintointracellularionicsignaling//TIBS.– 1986, 11 (11): 450–455.

2317. Uhlén P., Laestadius A., Jahnukainen T. et al. α-haemolysin of uropathogenic E. coli induces Ca2+ oscillations in renal epithelial cells // Nature. – 2000, 277: 694–697.

2318. Uozumi Y., Nawashiro H., Sato S. et al.Targetedincreaseincerebralbloodflowbytranscranialnearinfrared laser irradiation // Lasers in Surgery and Medicine. – 2010, 42 (6): 566–576.

2319. Usumez A., Cengiz B., Oztuzcu S. et al. Effects of laser irradiation at different wavelengths (660, 810, 980, and 1,064 nm) on mucositis in an animal model of wound healing // Lasers in Medical Science. – 2014, 29 (6): 1807–1813. doi: 10.1007/s10103-013-1336-z.

2320. Vagish Kumar L.S. Lasers in the management of chemoradiotherapy-induced oral mucositis // J. Cancer Res. Ther. – 2015, 11 (4): 1042. doi: 10.4103/0973-1482.150365.

2321. Valenzuela S., Lopez-Jornet P. Effects of low-level laser therapy on burning mouth syndrome // J. Oral Rehabil. – 2017, 44 (2): 125–132. doi: 10.1111/joor.12463.

2322. Van de Velde V., Quaghebeur M., De Porre J. et al. Low-level lazer therapy in the treatment of oral mucositis on an adult hematology and a pediatric hemato-oncology ward // 37th EBMT Annual Congress. – Paris, 2011, 31 (2). N1244.

2323. van Kooten D.W., Maciunas R.J., Carver R.S. Low-level CO2 laser–induced release of 51chromium from canine 2C5 gliosarcoma cells // Lasers in Surgery and Medicine. – 1993, 13 (5): 517–521.

2324. Velez-Gonzalez M., Urrea-Arbelaez A., Nicolas M. et al. Treatment of relapse in herpes simplex on labial and facial areas and of primary herpes simplex on genital areas and “area pudenda” with low-power He-Ne laser orAcyclovir administered orally // Proc. SPIE 2630, Effects of Low-Power Light on Biological Systems. – 1996. doi: 10.1117/12.230040.

2325. Verdi C.J. Cancer therapy and oral mucositis. An appraisal of drug prophylaxis // Drug Saf. – 1993, 9 (3): 185–195.

2326. Vescovi P., Giovannacci I., Merigo E. et al. Tooth extractions in high-risk patients under bisphosphonate therapy and previously affected with osteonecrosis of the jaws: surgical protocol supported by low-level laser therapy // J. Craniofacial Surg. – 2015, 26 (3): 696–699. doi: 10.1097/scs.0000000000001665.

2327. Vickers A.J., Straus D.J., Fearon B., Cassileth B.R. Acupuncture for postchemotherapy fatigue: a phase II study // J. Clin. Oncol. – 2004, V. 22(9): 1731–1735.

2328. Vidović Juras D., Lukac J., Cekić-Arambasin A. et al. Effects of low-level laser treatment on mouth dryness // Coll.Antropol. – 2010, 34 (3): 1039–1043.

2329. Vieira K.A., Bastos C.M., Vitor M.G.C. et al. Use of low-level laser therapy on children aged 1 to 5 years with energy-protein malnutrition: A clinical trial // Medicine (Baltimore). – 2018, 97 (17): e0538. doi: 10.1097/ MD.0000000000010538.

2330. Vitale M.C., Modaffari C., Decembrino N. et al. Preliminary study in a new protocol for the treatment of oralmucositisinpediatricpatientsundergoinghematopoieticstemcelltransplantation(HSCT)andchemotherapy (CT) // Lasers in Medical Science. – 2017, 32 (6): 1423–1428. doi: 10.1007/s10103-017-2266-y.

953

Рекомендовано к покупке и изучению сайтом МедУнивер - https://meduniver.com/

Лазерная терапия в онкологии

2331. Voskanyan K., Vorozhtsova S., Abrosimova A. et al. Laser light induced modification of the mice peripheral blood parameters and the number of bone marrow karyocytes after the action of ionizing radiation // Journal of Physical Science andApplication. – 2012, 2 (2): 7–11.

2332. Voskanyan K., Vorozhtsova S., Abrosimova A. et al. Reduction of radiation damage in mice after acute and prolonged irradiation with gamma rays by means of laser device // Journal of Physical Science andApplication. – 2014, 4 (8): 501–506.

2333. Voskanyan K., Vorozhtsova S.,AbrosimovaA. et al.The effectiveness of radiation damage reduction in mice by laser light in dependence of the time interval between exposures // Journal of Physical Science and Application. – 2015, 5 (4): 291–295. doi: 10.17265/2159-5348/2015.04.008.

2334. Wadhawan R., Solanki G., Bhandari A. et al. Role of laser therapy in dentistry: a review // Int. J. Biomed. Res. – 2014, 5 (3): 153–157. doi: https://doi.org/10.7439/ijbr.v5i3.528.

2335. Walker J. Relief from chronic pain by low power laser irradiation // Neuroscience Letters – 1983, 43 (2): 339–344. doi.org/10.1016/0304-3940(83)90211-2.

2336. Walker J.B., Swartzwelder H.S., Bondy S.C. Suppression of hippocampal epileptiform activity in vitro after laser exposure // Laser Therapy. – 2005, 14 (0_Pilot_Issue_2): 19–21.

2337. Wallingford J.В., Ewald A.J., Harland R.M., Fraser S.E. Calcium signaling during convergent extension in Xenopus // Curr. Biol. – 2001, 11 (9): 652–661.

2338. Wang X.-Y., Ma W.-J., Liu C.-S., Li Y.-X. Effect of low-level laser therapy on allergic asthma in rats // Lasers in Medical Science. – 2014, 29 (3): 1043–1450. doi: 10.1007/s10103-013-1456-5.

2339. Warde P., O’Sullivan B.,Aslanidis J. et al. APhase III placebo-controlled trial of oral pilocarpine in patients undergoing radiotherapy for head-and-neck cancer // Int. J. Radiat. Oncol. Biol. Phys. – 2002, 54 (1): 9–13. doi: 10.1016/s0360-3016(02)02890-0.

2340. Watman N.P., Crespo L., Davis B. et al. Differential effect on fresh and cultured T cells of PHA-induced changes in free cytoplasmic calcium: relation to IL-2 receptor expression, IL-2 production, and proliferation // Cellular Immun. – 1988, 111 (1): 158–166.

2341. Watters A.L., Epstein J.B., Agulnik M. Oral complications of targeted cancer therapies: a narrative literature review // Oral Oncol. – 2011, 47 (6): 441–448. doi: 10.1016/j.oraloncology.2011.03.028.

2342. Wedlock P., Shephard R.A., Little C., McBurney F. Analgesic effects of cranial laser treatment in two rat nociception models // Physiol. Behav. – 1996, 59: 445–448.

2343. Wedlock P.M., Shephard R.A. Cranial irradiation with GaAlAs laser leads to naloxone reversible analgesia in rats // Psychol. Rep. – 1996, 78 (3): 727–731.

2344. Wei X.B., Wang X.Y., Chen S.H. et al. The effect of ultra-violet laser on cancer //AbstractsASLMS Conference / Lasers in Surgery and Medicine. – 1988, 8 (2): 183–184. doi: 10.1002/lsm.1900080210.

2345. Weiss R.A., Deland M.M., Geronemus R.G., McDaniel D.H. Letter: Light-emitting diode photomodulation and radiation dermatitis // Dermatol. Surg. – 2011, 37 (6): 885–886. doi: 10.1111/j.1524-4725.2011.01988.x. 2346. Werneck C.E., Pinheiro A.L.B., Pacheco M.T. et al. Laser light is capable of inducing proliferation of carcinoma cells in culture:Aspectroscopic in vitro study // Photomedicine and Laser Surgery. – 2005, 23 (3): 300–303. doi: 10.1089/pho.2005.23.300.

2347. Whelan H.T., Connelly J.F., Hodgson B.D. et al. NASA light-emitting diodes for the prevention of oral mucositis in pediatric bone marrow transplant patients // Journal of Clinical Laser Medicine & Surgery. – 2002, 20 (6): 319–324.

2348. Wigg J. Use and response to treatment using low level laser therapy // Journal of Lymphoedema – 2009, 4 (5): 73–76.

2349. Wikramanayake T.C., Rodriguez R., Choudhary S. et al. Effects of the Lexington LaserComb on hair regrowth in the C3H/HeJ mouse model of alopecia areata // Lasers in Medical Science. – 2012, 27 (2): 431–436. doi: 10.1007/s10103-011-0953-7.

2350. Wikramanayake T.C., Villasante A.C., Mauro L.M. et al. Low-level laser treatment accelerated hair regrowth in a rat model of chemotherapy-induced alopecia (CIA) // Lasers in Medical Science. – 2013, 28 (3): 701–706. doi: 10.1007/s10103-012-1139-7.

2351. Wong R., Sagar S. Acupuncture treatment for chemotherapy-induced peripheral neuropathy – a case series //Acupunct. Med. – 2006, 24 (2): 87–91.

2352. Wong S.F., Wilder-Smith P. Pilot study of laser effects on oral mucositis in patients receiving chemotherapy // Cancer J. – 2002, 8 (3): 247–254.

2353. WorthingtonH.V.,ClarksonJ.E.,BryanG.etal.Interventionsforpreventingoralmucositisforpatientswith cancer receiving treatment // Cochrane Database Syst. Rev. – 2011, 13 (4): CD000978. doi: 10.1002/14651858. CD000978.pub5.

2354. Yamada H., Ogawa H. Comparative study of 60 mW diode laser therapy and 150 mW diode laser therapy in the treatment of postherpetic neuralgia // Laser Therapy. – 1995, 7 (2): 71–74.

954

Список литературы

2355. Yamaguchi N., Tsukamoto Y. The in vitro effects of semiconductor laser irradiation on inflammation: laser irradiation did not affect monocyte infiltration // Journal of Materials Science: Materials in Medicine. – 1994, 5 (8): 511–515. doi: 10.1007/bf00124882.

2356. Yamamoto R., Yamamoto T. Effectiveness of the treatment phase of two-phase complex decongestive physiotherapy for the treatment of extremity lymphedema // Int. J. Clin. Oncol. – 2007, 12 (6): 463–468. doi: 10.1007/s10147-007-0715-5.

2357. Yang H.Q., Wang Y.H., Chen J.X. et al. Efficacy of proliferation of HeLa cells under three different low-intensity red lasers irradiation // International Journal of Photoenergy. – 2012, Article ID 290796: 5. doi: 10.1155/2012/290796.

2358. Yang H.-W., Huang Y.-F. Treatment of burning mouth syndrome with a low-level energy diode laser // Photomedicine and Laser Surgery. – 2011, 29 (2): 123–125. doi: 10.1089/pho.2010.2787.

2359. Yang R., Wu Y., Ya L. et al. Risk factors of postoperative pulmonary complications after minimally invasive anatomic resection for lung cancer // Therapeutics and Clinical Risk Management. – 2019, 15 (1): 223–231. doi: 10.2147/TCRM.s195010.

2360. Yashiro Y., Duling B.R. Integrated Ca2+ signaling between smooth muscle and endothelium of resistance vessels // Circ. Res. – 2000, 87: 1048–1054.

2361. Yatskevich T., Semenova O., Moskvin S. Combined laser blood illumination by red (635 nm) and UV (365–405 nm) light in the treatment of small domestic animals with allergic dermatitis // Preprints. – 2017, 2017030186: doi: 10.20944/preprints201703.0186.v1.

2362. Yoshida K. Current considerations for low-level laser therapy/photobiomodulation therapy in the management of side effects of chemoradiation therapy for cancer // Photomedicine and Laser Surgery. – 2017, 35 (9): 457–458. doi: 10.1089/pho.2017.4322.

2363. Young S., Bolton P., Dyson M. et al. Macrophage responsiveness to light therapy // Lasers in Surgery and Medicine. – 1989, 9 (5): 497–505.

2364. Yu H.S., Chang K.L., Yu C.L. et al. Low-energy helium-neon laser irradiation stimulates interleukin-1 alpha and interleukin-8 release from cultured human keratinocytes //The Journal of Investigative Dermatology. – 1996, 107 (4): 593–596.

2365. Yu H.S., Chang K.L., Yu C.L. et al. Low-energy heliumneon laser irradiation stimulates interleukin-1 alpha and interleukin-8 release from cultured human keratinocytes // J. Invest. Dermatol. – 1996, 107 (4): 593–596. 2366. Yu H.S., Wu C.S., Yu C.L. et al. Helium-neon laser irradiation stimulates migration and proliferation in melanocytes and induces repigmentation in segmental-type vitiligo // J. Invest. Dermatol. – 2003, 120 (1): 56–64. doi: 10.1046/j.1523-1747.2003.12011.x.

2367. Yu W., Naim J.O., Lanzafame R.J. The effect of laser irradiation on the release of bFGF from 3T3 fibroblasts // Photochemistry and Photobiology. – 1994, 59(2): 167–170. doi: 10.1111/j.1751-1097.1994.tb05017.x. 2368. Zacchigna S., Biasotto M., Zanatta F. Authors’ reply // Am. J. Pathol. – 2014, 184 (4): 1251–1252. doi: 10.1016/j.ajpath.2014.02.001.

2369. Zadik Y., Arany P.R., Fregnani E.R. et al. Systematic review of photobiomodulation for the management of oral mucositis in cancer patients and clinical practice guidelines // Support Care Cancer. – 2019, 27 (10): 3969–3983. doi: 10.1007/s00520-019-04890-2.

2370. Zaichkinaa S.I., Rozanovaa O.M., Dyukinaa A.R. Influence of low-dose-rate red and near-infrared radiations on the level of reactive oxygen species, the genetic apparatus and the tumor growth in mice in vivo // Biophysics. – 2013, 58 (5): 712–717. doi: 10.1134/S0006350913050199.

2371. Zalesskaya G.A., Batay L.E., Koshlan I.V. et al. Combined impact of gamma and laser radiation on peripheral blood of rats in vivo // Journal of Applied Spectroscopy. – 2017, 84 (5): 796–803. doi: 10.1007/s10812- 017-0547-7.

2372. Zanin T., Zanin F., Carvalhosa A.A. et al. Use of 660-nm diode laser in the prevention and treatment of human oral mucositis induced by radiotherapy and chemotherapy // Photomedicine and Laser Surgery. – 2010, 28 (2): 233–237. doi: 10.1089/pho.2008.2242.

2373. Zarei M., Wikramanayake T.C., Falto-Aizpurua L. et al. Low level laser therapy and hair regrowth: an evidence-based review // Lasers in Medical Science. – 2016, 31 (2): 363–371. doi: 10.1007/s10103-015-1818-2. 2374. Žarković N., Kubović M., Jurin M. et al. The application of combined GaAs laser and radiation therapy in murine fibrosarcoma treatment //AbstractsASLMS Conference / Lasers in Surgery and Medicine. – 1988, 8 (2): 183. doi: 10.1002/lsm.1900080210.

2375. Zecha J.A., Raber-Durlacher J.E., Nair R.G. et al. Low level laser therapy/photobiomodulation in the management of side effects of chemoradiation therapy in head and neck cancer: part 1: mechanisms of action, dosimetric, and safety considerations // Supportive Care in Cancer. – 2016, 24 (6): 2781–2792. doi: 10.1007/ s00520-016-3152-z.

955

Рекомендовано к покупке и изучению сайтом МедУнивер - https://meduniver.com/

Лазерная терапия в онкологии

2376. Zecha J.A., Raber-Durlacher J.E., Nair R.G. et al. Low-level laser therapy/photobiomodulation in the management of side effects of chemoradiation therapy in head and neck cancer: part 2: proposed applications and treatment protocols // Supportive Care in Cancer. – 2016(1), 24 (6): 2793–2805. doi: 10.1007/s00520-016-3153-y. 2377. Zhang J., Li X., Xu J., Ernst E. Laser acupuncture for the treatment of asthma in children: a systematic review of randomized controlled trials // J.Asthma. – 2012, 49 (7): 773–737. doi: 10.3109/02770903.2012.691194. 2378. Zhang W., Wu C., Pan W. et al. Low-power helium-neon laser irradiation enhances the expression ofVEGF in murine myocardium // Chin. Med. J. – 2004, 117 (10): 1476–1480.

2379. Zharinov G.M., Zimin A.A., Samoilova K.A. et al. Late radiation lesions of urinary bladder and rectum in patients with prostate cancer after external radiation therapy and phototherapy with low power near infrared laser // Laser Therapy. – 2010, 19 (2): 89–95.

2380. Zhu N.W., Perks C.M., Burd A.R., Holly J.M. Changes in the levels of integrin and focal adhesion kinase (FAK) in human melanoma cells following 532 nm laser treatment // Int. J. Cancer. – 1999, 82 (3): 353–358. doi. 10.1002/(SICI)1097-0215(19990730)82: 3<353: :AID-IJC8>3.0.CO;2-4|.

2381. Zimmermann M. Studies on therapeutic efficacy of a He-Ne laser // Dtsch. Z. Mund Kiefer Gesichtschir. – 1990, 14 (4): 313–319. [Article in German].

2382. Zyryanov B.N., Evtushenko V.A., Evtushenko G.S. et al. Copper-vapor low-intensity laser therapy // Proc. SPIE, CIS Selected Papers: Laser Use in Oncology. – 1996, 2728: 100–107. doi: 10.1117/12.229477.

2383. Zyryanov B.N., Evtushenko V.A., Evtushenko G.S. et al. Laser therapy in oncologic patient // The book seventh International Congress onAnti-Cancer Treatment, Paris. – 1997. – P. 1234.

956

Рекомендовано к покупке и изучению сайтом МедУнивер - https://meduniver.com/

958

959

Рекомендовано к покупке и изучению сайтом МедУнивер - https://meduniver.com/