1. Кит О.И., Франциянц Е.М., Котиева И.М., Каплиева И.В., Трепитаки Л.К., Бандовкина В.А., Розенко Л.Я., Черярина Н.Д., Погорелова Ю.А. Некоторые механизмы повышения злокачественности меланомы на фоне хронической боли у самок мышей. Рос. журн. боли. 2017; 53 (2): 14–20.
Kit O.I., Frantsiyants E.M., Kotieva I.M., Kaplieva I.V., Trepitaki L.K., Bandovkina V.A., Rozenko L Ya., Cheryarina N.D., Pogorelova Yu.A. Some mechanisms of increasing malignancy of B16/F10 melanoma in female mice with chronic pain. Rossiyskiy zhurnal boli = Russian Journal of Pain. 2017; 53 (2): 14–20. [In Russian].
2. Almholt K., Lund L.R., Rygaard J., Nielsen B.S., Danø K., Rømer J., Johnsen M. Reduced metastasis of transgenic mammary cancer in urokinase-deficient mice. Int. J. Cancer. 2005; 113 (4): 525–532. doi 10.1002/ijc.20631.
3. Bruncko M., McClellan W.J., Wendt M.D., Sauer D.R., Geyer A., Dalton C.R., Kaminski M.A., Weitzberg M., Gong J., Dellaria J.F., Mantei R., Zhao X., Nienaber V.L., Stewart K., Klinghofer V., Bouska J., Rockway T.W., Giranda V.L. Naphthamidine urokinase plasminogen activator inhibitors with improved pharmacokinetic properties. Bioorg. Med. Chem. Lett. 2005; 15: 93–98. doi 10.1016/j.bmcl.2004.10.026.
4. Cathcart J., Pulkoski-Gross A., Cao J. Targeting matrix metalloproteinases in cancer: Bringing new life to old ideas. Genes Dis. 2015; 2: 26–34. doi 10.1016/j.gendis.2014.12.002.
5. Fernández-Lao C., Cantarero-Villanueva I., Fernández-de-las-Peñas C., Del-Moral-Ávila R., Menjón-Beltrán S., Arroyo-Morales M. Widespread mechanical pain hypersensitivity as a sign of central sensitization after breast cancer surgery: comparison between mastectomy and lumpectomy. Pain Med. 2011; 12 (1): 72–78. doi 10.1111/j.1526-4637.2010.01027.
6. Frese K.K., Tuveson D.A. Maximizing mouse cancer models. Nat. Rev. Cancer. 2007; 7 (9): 645–58. doi 10.1038/nrc2192.
7. Gutierrez L.S., Schulman A., Brito-Robinson T., Noria F., Ploplis V.A., Castellino F.J. Tumor development is retarded in mice lacking the gene for urokinase-type plasminogen activator or its inhibitor, plasminogen activator inhibitor-1. Cancer Res. 2000; 60 (20): 5839–5847.
8. Heinemann V., Ebert M.P., Laubender R.P., Bevan P., Mala C., Boeck S. Phase II randomised proof-of-concept study of the urokinase inhibitor upamostat (WX-671) in combination with gemcitabine compared with gemcitabine alone in patients with non-resectable, locally advanced pancreatic cancer. Br. J. Cancer. 2013; 108 (4): 766–770. doi 10.1038/bjc.2013.62.
9. Jankun J., Keck R.W., Selman S.H. Epigallocatechin-3-gallate prevents tumor cell implantation/growth in an experimental rat bladder tumor model. Int. J. Oncol. 2014; 44: 147–152. doi 10.3892/ijo. 2013.2174.
10. Jankun J., Selman S.H., Aniola J., Skrzypczak-Jankun E. Nutraceutical inhibitors of urokinase: Potential applications in prostate cancer prevention and treatment. Oncol. Rep. 2006; 16: 341–346.
11. Katz B.A., Sprengeler P.A., Luong C., Verner E., Elrod K., Kirtley M., Janc J., Spencer J.R., Breitenbucher J.G., Hui H., McGee D., Allen D., Martelli A., Mackman R.L. Engineering inhibitors highly selective for the S1 sites of Ser190 trypsin-like serine protease drug targets. Chem. Biol. 2001; 8: 1107–1121. doi 10.1016/S1074-5521(01)00084-9.
12. Lampreht Tratar U., Horvat S., Cemaza M. Transgenic mouse models in cancer research. Front. Oncol. 2018; 8: 268. doi 10.3389/fonc.2018.00268.
13. Lewandoski M. Conditional control of gene expression in the mouse. Nat. Rev. Genet. 2001; 2 (10): 743–755.
14. Mahmood N., Mihalcioiu C., Rabbani S.A. Multifaceted role of the urokinase-type plasminogen activator (uPA) and its receptor (uPAR): Diagnostic, prognostic, and therapeutic applications. Front. Oncol. 2018; 8: 24. doi 10.3389/fonc.2018.00024.
15. Malfliet A., Leysen L., Pas R., Kuppens K., Nijs J., van Wilgen P., Huysmans E., Goudman L., Ickmans K. Modern pain neuroscience in clinical practice: applied to post-cancer, paediatric and sports-related pain. Braz. J. Phys. Ther. 2017; 21 (4): 225–232. doi 10.1016/j.bjpt.2017.05.009.
16. Ogilvie L.A., Kovachev A., Wierling C., Lange B.M., Lehrach H. Models of models: a translational route for cancer treatment and drug development. Front. Oncol. 2017; 7: 219. doi: 10.3389/fonc.2017.00219.
17. Pérez-Guijarro E., Day C.P., Merlino G., Zaidi M.R. Genetically engineered mouse models of melanoma. Cancer. 2017; 123 (S11): 2089–2103. doi 10.1002/cncr.30684.
18. Schmitt M., Harbeck N., Brünner N., Jänicke F., Meisner C., Mühlenweg B., Jansen H., Dorn J., Nitz U., Kantelhardt E.J., Thomssen C. Cancer therapy trials employing level-of-evidence-1 disease forecast cancer biomarkers uPA and its inhibitor PAI-1. Exp. Rev. Mol. Diagn. 2011; 11: 617–634. doi 10.1586/erm.11.47.
19. Walrath J.C., Hawes J.J., van Dyke T., Reilly K.M. Genetically engineered mouse models in cancer research. Adv. Cancer Res. 2010; 106: 113–164. doi 10.1016/S0065-230X(10)06004-5.
20. Wyganowska-Świątkowska M., Tarnowski M., Murtagh D., Skrzypczak-Jankun E., Jankun J. Proteolysis is the most fundamental property of malignancy and its inhibition may be used therapeutically (Review). Int. J. Mol. Med. 2018; 43 (1): 15–25. doi 10.3892/ijmm.2018.3983.
21. Zengel P., Ramp D., Mack B., Zahler S., Berghaus A., Muehlenweg B., Gires O., Schmitz S. Multimodal therapy for synergic inhibition of tumour cell invasion and tumour-induced angiogenesis. BMC Cancer. 2010; 10: 92. doi 10.1186/1471-2407-10-92.