ОКУЛО- И РЕТИНОТОКСИЧНОСТЬ ПРОТИВООПУХОЛЕВЫХ ПРЕПАРАТОВ НА ОСНОВЕ АЛКИЛИРУЮЩИХ АГЕНТОВ
Загрузок: 100
Просмотров: 69
PDF

Ключевые слова

ХИМИОТЕРАПИЯ
АЛКИЛИРУЮЩИЕ СОЕДИНЕНИЯ
РЕТИНОТОКСИЧНОСТЬ
РЕТИНОПАТИЯ
РЕПАРАЦИЯ ДНК

Как цитировать

Тронов, В., & Некрасова, Е. (2018). ОКУЛО- И РЕТИНОТОКСИЧНОСТЬ ПРОТИВООПУХОЛЕВЫХ ПРЕПАРАТОВ НА ОСНОВЕ АЛКИЛИРУЮЩИХ АГЕНТОВ. Вопросы онкологии, 64(5), 555–563. https://doi.org/10.37469/0507-3758-2018-64-5-555-563

Аннотация

Положительным итогом химиотерапии рака является увеличение длительности ремиссии и жизни леченых больных. Но на этом фоне стали проявляться и негативные вторичные эффекты химиотерапии. Эти эффекты снижают качество жизни леченых больных. К ним относятся офтальмологические осложнения. В обзоре приведены клинические данные об офтальмологической токсичности 7 представителей алкилирующих соединений и интерферона, используемых в химиотерапии. Большое внимание в обзоре уделено ретинотоксическим эффектам этих препаратов. Рассмотрен механизм их гено- и цитотоксического действия, роль в этом участников эксцизионной репарации - N-алкиладенин-Днк-гликозилазы и поли(АДФ-рибоза)-полимеразы (PARP1).

https://doi.org/10.37469/0507-3758-2018-64-5-555-563
Загрузок: 100
Просмотров: 69
PDF

Библиографические ссылки

Абрамов М.Е., Гуторов С.Л., Славина Е.Г Химиотерапия диссеминированной меланомы кожи с включением ингарона (у-ИФН) // российский биотерапевтический журнал. - 2009. - № 1 (8). - C. 64-74.

Логинова М.Ю., Тронов В.А., Белецкая Т.А. и др. радиорезистентность сетчатки: под действием у-излучения в сетчатке мышей формируются разрывы ДНК, увеличивается содержание белка р53, сопровождаемые репарацией ДНК и отсутствием апоптоза клеток // радиационная биология. радиоэкология. - 2008. - № 6 (48). - C. 698-704.

Островская Л.А., Филов В.А., Ивин Б.А., и др. Препараты класса нитрозоалкилмочевин в отечественной противоопухолевой химиотерапии // рос. биотер. журн. - 2004. - № 1 (3). - C. 24-13.

Abramson D.H., Dunkel I.J., Brodie S.E. et al. A phase I/ II study of direct intraarterial (ophthalmic artery) chemo therapy with melphalan for intraocular retinoblastoma initial results // Ophthalmology. - 2008. - № 8 (115). - P. 1398-1404.

Adhikari S., Toretsky J.A., Yuan L., Roy R. Magnesium, essential for base excision repair enzymes, inhibits substrate binding of N-methylpurine-DNA glycosylase // The Journal of biological chemistry. - 2006. - № 40 (281). - P. 29525-32.

Agarwal S., Ray B., Mehrotra R. SERS as an advanced tool for investigating chloroethyl nitrosourea derivatives complexation with DNA // International journal of biological macromolecules. - 2015. - № 81. - P. 891-7.

Agnihotri S., Gajadhar A.S., Ternamian C. et al. Alkylpurine- DNA-N-glycosylase confers resistance to temozolomide in xenograft models of glioblastoma multiforme and is associated with poor survival in patients // The Journal of clinical investigation. - 2012. - № 1 (122). - P. 253-266.

Ahel D., Horejs Z., Wiechens N. et al. Poly(ADP-ribose)-dependent regulation of DNA repair by the chromatin remodeling enzyme ALC1 // Science (New York, NY). - 2009. - № 5945 (325). - P. 1240-3.

Allocca M., Corrigan J.J., Fake K.R. et al. PARP inhibitors protect against sex- and AAG-dependent alkylation-induced neural degeneration // Oncotarget. - 2017. - № 40 (8). - P. 68707-68720.

Anders C.K., Winer E.P., Ford J.M. et al. Poly(ADP-Ribose) polymerase inhibition: «targeted» therapy for triple-negative breast cancer // Clinical cancer research: an official journal of the American Association for Cancer Research. - 2010. - № 19 (16). - P. 4702-10.

Bignami M., O'Driscoll M., Aquilina G., Karran P. Unmasking a killer: DNA O(6)-methylguanine and the cytotoxicity of methylating agents // Mutation research. - 2000. - № 2-3 (462). - P. 71-82.

Boeck K., Hofmann S., Klopfer M. et al. Melanoma-associated paraneoplastic retinopathy: case report and review of the literature // The British journal of dermatology. -1997. - № 3 (137). - P. 457-60.

Boiteux S., Guillet M. Abasic sites in DNA: repair and biological consequences in Saccharomyces cerevisiae // DNA repair. - 2004. - № 1 (3). - P. 1-12.

Cao W., Tombran-Tink J., Elias R. et al. In vivo protection of photoreceptors from light damage by pigment epithelium-derived factor // Investigative ophthalmology & visual science. - 2001. - № 7 (42). - P. 1646-52.

Chamberlain M.C. Temozolomide: therapeutic limitations in the treatment of adult high-grade gliomas // Expert review of neurotherapeutics. - 2010. - № 10 (10). - P. 1537-44.

Chauveinc L., Sola-Martinez M.T, Martin-Duverneuil M. et al. Intra arterial chemotherapy with ACNU and radiotherapy in inoperable malignant gliomas // Journal of neuro-oncology. - 1996. - № 2 (27). - P. 141-147.

Chen C., Damek D., Gaspar L.E. et al. Phase I trial of hypofractionated intensity-modulated radiotherapy with temozolomide chemotherapy for patients with newly diagnosed glioblastoma multiforme // International journal of radiation oncology, biology, physics. -2011. - № 4 (81). - P. 1066-74.

Cohen S.-Y, Bourgeois H., Corbe C. et al. Randomized clinical trial France DMLA2: effect of trimetazidine on exudative and nonexudative age-relatedmacular degeneration // Retina (Philadelphia, Pa.). - 2012. - № 4 (32). - P. 834-43.

Crosbie P.A.J., Watson A.J., Agius R. et al. Elevated N3-methylpurine-DNA glycosylase DNA repair activity is associated with lung cancer // Mutation research. - 2012. - № 1-2 (732). - P. 43-46.

Curtin N.J., szabo C. therapeutic applications of PARP inhibitors: anticancer therapy and beyond // Molecular aspects of medicine. - 2013. - № 6 (34). - P. 1217-1256.

Darkes M.J.M., Plosker G.L., Jarvis B. Temozolomide: A Review of its Use in the treatment of Malignant Gliomas, Malignant Melanoma and Other Advanced Cancers // American Journal of Cancer. - 2002. - № 1 (1). - P. 55-80.

Davar D., Tarhini A.A., Kirkwood J.M. Adjuvant therapy for melanoma // Cancer journal. - 2012. - № 2 (18). - P. 192-202.

Dixon M., Woodrick J., Gupta s. et al. Naturally occurring polyphenol, morin hydrate, inhibits enzymatic activity of N-methylpurine DNA glycosylase, a DNA repair enzyme with various roles in human disease // Bioorganic & medicinal chemistry. - 2015. - № 5 (23). - P. 1102-1111.

Eguchi Y, shimizu S., Tsujimoto Y Intracellular ATP levels determine cell death fate by apoptosis or necrosis // Cancer research. - 1997. - № 10 (57). - P. 1835-40.

Ensminger M., Iloff L., Ebel C. et al. DNA breaks and chromosomal aberrations arise when replication meets base excision repair // the Journal of cell biology. - 2014. - № 1 (206). - P. 29-43.

Faustino-Rocha A.I., Ferreira R., Oliveira P.A. et al. N-Methyl-N-nitrosourea as a mammary carcinogenic agent // tumour biology: the journal of the International society for Oncodevelopmental Biology and Medicine. - 2015. - № 12 (36). - P. 9095-117.

Francis J.H., schaiquevich P., Buitrago E. et al. Local and systemic toxicity of intravitreal melphalan for vitreous seeding in retinoblastoma: a preclinical and clinical study // Ophthalmology. - 2014. - № 9 (121). - P. 1810-7.

Ghassemi F., shields C.L. Intravitreal melphalan for refractory or recurrent vitreous seeding from retinoblastoma // Archives of ophthalmology (Chicago, Ill.: 1960). - 2012. - № 10 (130). - P. 1268-71.

Gonzaga P.E., Potter P.M., Niu T.Q. et al. Identification of the cross-link between human O6-methylguanine-DNA methyltransferase and chloroethylnitrosourea-treated DNA // Cancer research. - 1992. - № 21 (52). - P. 6052-6058.

Greenberg H.S., Ensminger W.D., Chandler W.F. et al. Intra-arterial BCNU chemotherapy for treatment of malignant gliomas of the central nervous system // Journal of neurosurgery. - 1984. - № 3 (61). - P. 423-9.

Grimson B.S., Mahaley M.S., Dubey H.D., Dudka L. Ophthalmic and central nervous system complications following intracarotid BCNU (Carmustine) // Journal of clinical neuro-ophthalmology. - 1981. - № 4 (1). - P. 261-4.

Ha C.S., Michalek J.E., Elledge R. et al. p53-based strategy to reduce hematological toxicity of chemotherapy: A proof of principle study // Molecular oncology. - 2016. - № 1 (10). - P. 148-56.

Hayasaka S., Nagaki Y., Matsumoto M., sato s. Interferon associated retinopathy // Br. J. Ophthalmol. - 1998. - № 3 (82). - P. 323-325.

Hejny C., sternberg P., Lawson D.H. et al. Retinopathy associated with high-dose interferon alfa-2b therapy // American journal of ophthalmology. - 2001. - № 6 (131). - P. 782-7.

Hofseth L.J., Khan M.A., Ambrose M. et al. The adaptive imbalance in base excision-repair enzymes gener ates microsatellite instability in chronic inflammation // the Journal of clinical investigation. - 2003. - № 12 (112). - P. 1887-94.

Hu J., Guo X., Yang L. Morin inhibits proliferation and self-renewal of CD133 melanoma cells by upregulating miR-216a // Journal of pharmacological sciences. -2018.

Imperia P.S., Lazarus H.M., Lass J.H. Ocular complications of systemic cancer chemotherapy // survey of Ophthalmology. - 1989. - № 3 (34). - P. 209-230.

Khawly J.A., Rubin P., Petros W. et al. Retinopathy and optic neuropathy in bone marrow transplantation for breast cancer // Ophthalmology. - 1996. - № 1 (103). - P. 87-95.

Kisby G.E., Lesselroth H., Olivas A. et al. Role of nucleotide-and base-excision repair in genotoxin-induced neuronal cell death // DNA repair. - 2004. - № 6 (3). - P. 617-627.

Kupersmith M.J., Frohman L.P., Choi I.S. et al. Visual system toxicity following intra-arterial chemotherapy // Neurology. - 1988. - № 2 (38). - P. 284-9.

Kupersmith M.J., Teiple W.H., Holopigian K. et al. Maculopathy caused by intra-arterially administered cisplatin and intravenously administered carmustine // American journal of ophthalmology. - 1992. - № 4 (113). - P. 435-8.

Lheureux S., Bruce J.P., Burnier J. V et al. somatic BRCA1/2 Recovery as a Resistance Mechanism After Exceptional Response to Poly (ADP-ribose) Polymerase Inhibition // Journal of clinical oncology. - 2017. - № 11 (35). - P. 1240-1249.

Lin F-L., Lin C.-H., Ho J.-D. et al. The natural retinopro-tectant chrysophanol attenuated photoreceptor cell apop-tosis in an N-methyl-N-nitrosourea-induced mouse model of retinal degenaration // scientific reports. - 2017. - № 7. - P. 41086.

Ma Z., Wei Q., Dong G. et al. DNA damage response in renal ischemia-reperfusion and ATP-depletion injury of renal tubular cells // Biochimica et biophysica acta. - 2014. - № 7 (1842). - P. 1088-96.

Martin D.S., Schwartz G.K. Chemotherapeutically induced DNA damage, ATP depletion, and the apoptotic biochemical cascade // Oncology research. - 1997. - № 1 (9). - P. 1-5.

Matus G., Dicato M., Focan C. Cancer associated retinopathy (CAR). Two clinical cases and review of the literature // Revue medicale de Liege. - 2007. - № 3 (62). - P. 166-9.

Meira L.B., Moroski-Erkul C.A., Green S.L. et al. Aag-ini-tiated base excision repair drives alkylation-induced retinal degeneration in mice // Proceedings of the National Academy of sciences of the United states of America. - 2009. - № 3 (106). - P. 888-893.

Mocellin S., Pasquali S., Rossi C.R., Nitti D. Interferon alpha adjuvant therapy in patients with high-risk melanoma: a systematic review and meta-analysis // Journal of the National Cancer Institute. - 2010. - № 7 (102). - P. 493-501.

Monzon J.G., Hammad N., Stevens S.D., Dancey J. Retinopathy associated with adjuvant high-dose interferon-a2b in a patient with resected melanoma: a case report and review of the literature // The oncologist. - 2012. - № 3 (17). - P. 384-7.

Ockenfels M., Lisch W. Ocular complications of adjuvant interferon therapy for malignant melanoma: a review // Hautarzt. - 2003. - № 2 (54). - P. 144-7.

Pabla N., Huang S., Mi Q.-s. et al. ATR-Chk2 signaling in p53 activation and DNA damage response during cisplatin-induced apoptosis // The Journal of biological chemistry. -2008. - № 10 (283). - P. 6572-6583.

Pföhler C., Haus A., Palmowski A. et al. Melanoma-associated retinopathy: high frequency of subclinical findings in patients with melanoma // The British journal of dermatology. - 2003. - № 1 (149). - P. 74-78.

Reid J.M., Kuffel M.J., Miller J.K. et al. Metabolic activation of dacarbazine by human cytochromes P450: the role of CYP1A1, CYP1A2, and CYP2E1 // Clinical cancer research: an official journal of the American Association for Cancer Research. - 1999. - № 8 (5). - P. 2192-7.

Robins P., Harris A.L., Goldsmith I., Lindahl T. Cross-linking of DNA induced by chloroethylnitrosourea is presented by O6-methylguanine-DNA methyltransferase // Nucleic acids research. - 1983. - № 22 (11). - P. 7743-58.

Rottenberg S., Jaspers J.E., Kersbergen A. et al. High sensitivity of BRCA1-deficient mammary tumors to the PARP inhibitor AZD2281 alone and in combination with platinum drugs // Proceedings of the National Academy of Sciences of the United States of America. -2008. - № 44 (105). - P. 17079-84.

Saito Т., Yokoyame М., Himori Т. et al. Phase I and preliminary phase II study of l-(4-amino-2-methyl-5-pyrimidinyl)methyl 3-(2-chloroethyl)-3-nitrosourea hydrochloride (ACNU) administered by intermittent dose schedule // Japanese Journal of Cancer and Chemotherapy. - 1977. - № 4. - P. 991-1004

Sato K., Kitajima Y, Koga Y et al. The effect of o6-methylguanine-DNA methyltransferase (MGMT) and mismatch repair gene (hMLH1) status on the sensitivity to alkylating agent 1-(4-amino-2-methyl-5-pyrimidinyl) methyl-3-(2-chloroethyl)-3-nitrosourea(ACNU) in gallbladder carcinoma cells // Anticancer research. - 2005. -№6B (25). - P. 4021-8

Schreiber S., Prox-Vagedes V., Elolf E. et al. Bilateral posterior RION after concomitant radiochemotherapy with temozolomide in a patient with glioblastoma multiforme: a case report // BMC cancer. - 2010. - №10. - P. 520

Shimamura Y., Chikama M., Tanimoto T. et al. Optic nerve degeneration caused by supraophthalmic carotid artery infusion with cisplatin and ACNU. Case report // Journal of Neurosurgery. - 1990. - № 2 (72). - P. 285-288.

Shingleton B.J., Bienfang D.C., Albert D.M. et al. Ocular toxicity associated with high-dose carmustine // Archives of ophthalmology (Chicago, Ill.: 1960). - 1982. - № 11 (100). -P. 1766-72.

Smith S.J., Smith B.D. Evaluating the risk of extraocular tumour spread following intravitreal injection therapy for retinoblastoma: a systematic review // The British journal of ophthalmology. - 2013. - № 10 (97). - P. 1231-6.

Sobol R.W., Kartalou M., Almeida K.H. et al. Base excision repair intermediates induce p53-independent cytotoxic and genotoxic responses // The Journal of biological chemistry. -2003. - № 41 (278). - P. 39951-9.

Sobol R.W., Prasad R., Evenski A. et al. The lyase activity of the DNA repair protein beta-polymerase protects from DNA-damage-induced cytotoxicity // Nature. - 2000. - № 6788 (405). - P. 807-810.

Stoffelns B.M. Interferon causes ischemic ocular diseases -case studies and review of the literature // Klinische Monatsblatter fur Augenheilkunde. - 2006. - № 5 (223).- P. 367-71.

Struwe M., Greulich K.-O., Junker U. et al. Detection of photogenotoxicity in skin and eye in rat with the photo comet assay // Photochem Photobiol. Sci. - 2008. - № 2 (7). - P. 240-9.

Treudler R., Georgieva J., Geilen C.C., Orfanos C.E. Dacarbazine but not temozolomide induces phototoxic dermatitis in patients with malignant melanoma // Journal of the American Academy of Dermatology. - 2004. - № 5 (50). - P. 783-5.

Tsubura A., Lai Y-C., Miki H. et al. Animal models of N-Methyl-N-nitrosourea-induced mammary cancer and retinal degeneration with special emphasis on therapeutic trials // In vivo. - 2011. - № 1 (25). - P. 11-22.

Wang Y., Chen X., Zhang Z. et al. Comparison of the clinical efficacy of temozolomide (TMZ) versus nimustine (ACNU)-based chemotherapy in newly diagnosed glioblastoma // Neurosurgical review. - 2014. - № 1 (37). - P. 73-78.

Wilczek Z.M. Experimental intraocular penetration of dacarbazine // American journal of ophthalmology. - 1977. - № 3 (84). - P. 299-304.

Woodhouse B.C., Dianova I.I., Parsons J.L., Dianov G.L. Poly(ADP-ribose) polymerase-1 modulates DNA repair capacity and prevents formation of DNA double strand breaks // DNA repair. - 2008. - № 6 (7). - P. 932-940.

Xu J., Li L., Xiong J. et al. Cyclophosphamide Combined with Bone Marrow Mesenchymal Stromal Cells Protects against Bleomycin-induced Lung Fibrosis in Mice // Annals of clinical and laboratory science. - 2015. - № 3 (45). - P. 292-300.

Ying W., Sevigny M.B., Chen Y, Swanson R.A. Poly(ADP-ribose) glycohydrolase mediates oxidative and excitotoxic neuronal death // Proceedings of the National Academy of Sciences of the United States of America. - 2001. - № 21 (98). - P. 12227-32.

Yoshizawa K., Sasaki T, Uehara N. et al. N -ethyl- N -nitrosourea induces retinal photoreceptor damage in adult rats // Journal of toxicologic pathology. - 2012. - № 1 (25). - P. 27-35.

Лицензия Creative Commons

Это произведение доступно по лицензии Creative Commons «Attribution-NonCommercial-NoDerivatives» («Атрибуция — Некоммерческое использование — Без производных произведений») 4.0 Всемирная.

© АННМО «Вопросы онкологии», Copyright (c) 2018