JMB-HEADER RAS-JOURNALS EIMB Pleiades Publishing

RUS

             

ENG

YearIMPACT-FACTOR
2022  1,200
2021  1,540
2020  1,374
2019  1,023
2018  0,932
2017  0,977
2016  0,799
2015  0,662
2014  0,740
2013  0,739
2012  0,637
2011  0,658
2010  0,654
2009  0,570
2008  0,849
2007  0,805
2006  0,330
2005  0,435
2004  0,623
2003  0,567
2002  0,641
2001  0,490
2000  0,477
1999  0,762
1998  0,785
1997  0,507
1996  0,518
1995  0,502
Vol 45(2011) N 3 p. 375-391;
V.V. Pleshkan1,2, M.V. Zinovyeva1*, E.D. Sverdlov2,1

Melanoma: Surface Markers as the First Point of Targeted Delivery of Therapeutic Genes in Multilevel Gene Therapy

1Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, 117997
2Institute of Molecular Genetics, Russian Academy of Sciences, Moscow, 123182

*mzinov@humgen.siobc.ras.ru
Received - 2010-10-06; Accepted - 2010-11-12

Melanoma is one of the most malignant tumors that metastasizes aggressively by lymphatic and hematogenous routes. Because of the resistance of melanoma cells to many types of chemotherapy, the disease causes a high mortality rate. High hopes are pinned on gene therapeutic approaches to melanoma treatment. At present, one of the main problems of the efficient use of postgenomic-generation therapeutic means is the lack of optimal techniques for delivering foreign genetic material to the patient's target cells. Specific surface markers of melanoma cells can be considered as promising therapeutic targets. The review describes currently known melanoma-specific receptors and melanoma stem cells and considers the data on melanoma antigens presented on the cell surface by major histocompatibility complex proteins. The ability of surface proteins to be internalized might be successfully used to develop methods of targeted delivery of therapeutic gene constructs. In conclusion, a concept of multilevel gene therapy and the possible role of surface determinants as targets of gene system delivery to the tumor are discussed.

melanoma, surface antigens, receptors, targeted delivery, gene therapy



JMB-FOOTER RAS-JOURNALS