34
views
0
recommends
+1 Recommend
1 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Complex of C 60 Fullerene with Doxorubicin as a Promising Agent in Antitumor Therapy

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The main aim of this work was to evaluate the effect of doxorubicin in complex with C 60 fullerene (C 60 + Dox) on the growth and metastasis of Lewis lung carcinoma in mice and to perform a primary screening of the potential mechanisms of C 60 + Dox complex action. We found that volume of tumor from mice treated with the C 60 + Dox complex was 1.4 times less than that in control untreated animals. The number of metastatic foci in lungs of animals treated with C 60 + Dox complex was two times less than that in control untreated animals. Western blot analysis of tumor lysates revealed a significant decrease in the level of heat-shock protein 70 in animals treated with C 60 + Dox complex. Moreover, the treatment of tumor-bearing mice was accompanied by the increase of cytotoxic activity of immune cells. Thus, the potential mechanisms of antitumor effect of C 60 + Dox complex include both its direct action on tumor cells by inducing cell death and increasing of stress sensitivity and an immunomodulating effect. The obtained results provide a scientific basis for further application of C 60 + Dox nanocomplexes as treatment agents in cancer chemotherapy.

          Related collections

          Most cited references32

          • Record: found
          • Abstract: found
          • Article: not found

          [60]fullerene is a powerful antioxidant in vivo with no acute or subacute toxicity.

          In the present work, we report the effects of C(60)-pretreatments on acute carbon tetrachloride intoxication in rats, a classical model for studying free-radical-mediated liver injury. Our results show that aqueous C(60) suspensions prepared without using any polar organic solvent not only have no acute or subacute toxicity in rodents but they also protect their livers in a dose-dependent manner against free-radical damage. To be sure, according to histopathological examinations and biological tests, pristine C(60) can be considered as a powerful liver-protective agent.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Role of angiogenesis in human tumor dormancy: animal models of the angiogenic switch.

            Tumor progression depends on sequential events, including a switch to the angiogenic phenotype (i.e., initial recruitment of blood vessels). Failure of a microscopic tumor to complete one or more early steps in this process may lead to delayed clinical manifestation of the cancer. Microscopic human cancers can remain in an asymptomatic, non-detectable, and occult state for the life of a person. Clinical and experimental evidence suggest that human tumors can persist for long periods of time as microscopic lesions that are in a state of dormancy (i.e., not expanding in tumor mass). Because it is well established that tumor growth beyond the size of 1-2 mm is angiogenesis-dependent, we hypothesized that presentation of large tumors is attributed to a switch to the angiogenic phenotype in otherwise microscopic, dormant tumors. Although clinically important, the biology of human tumor dormancy is poorly understood. The development of animal models which recapitulate the clinically observed timing and proportion of dormant tumors which switch to the angiogenic phenotype are reviewed here. The contributing molecular mechanisms involved in the angiogenic switch and different strategies for isolation of both angiogenic and non-angiogenic tumor cell populations from otherwise heterogeneous human tumor cell lines or surgical specimens are also summarized. Several imaging techniques have been utilized for the qualitative and quantitative detection of microscopic tumors in mice and their strengths and limitations are discussed. The animal models employed here permitted further studies of the angiogenic switch. These models also allowed development of an angiogenesis-based panel of blood and urine biomarkers that can be quantified and used to detect microscopic tumors before or during the angiogenic switch. If the information obtained from these animal models is translatable to the clinic, it may be possible in the future to liberate the management of cancer from a dependency on anatomical site years before it becomes symptomatic and detectable.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Natural killer cell developmental pathways: a question of balance.

              J Santo (2005)
              NK cells sit at the crossroads of innate and adaptive immunity and help coordinate tumor immunosurveillance and the immune response against pathogens. Balancing signals to NK cell precursors is crucial for their early development, when transcription factors compete to specify the different lymphocyte subsets. Despite an elaborate schema for NK cell development and differentiation, several major issues remain to be addressed, such as identifying the sites for NK cell maturation and defining the peripheral NK cell niche.
                Bookmark

                Author and article information

                Contributors
                psvit@bigmir.net
                realmed@i.com.ua
                gennadij_d@mail.ru
                prylut@ukr.net
                max_evstigneev@mail.ru
                iris@onconet.kiev.ua
                rpanchuk@ukr.net
                stoika@cellbiol.lviv.ua
                uwe.ritter@tu-ilmenau.de
                peter.scharff@tu-ilmenau.de
                Journal
                Nanoscale Res Lett
                Nanoscale Res Lett
                Nanoscale Research Letters
                Springer US (New York )
                1931-7573
                1556-276X
                29 December 2015
                29 December 2015
                2015
                : 10
                : 499
                Affiliations
                [ ]Taras Shevchenko National University of Kyiv, 64 Volodymyrska Str., 01601 Kyiv, Ukraine
                [ ]R.E. Kavetsky Institute of Experimental Pathology, Oncology and Radiobiology of NASU, Vasylkivska Str. 45, 03022 Kyiv, Ukraine
                [ ]Belgorod State University, Pobedy Str.85, 308015 Belgorod, Russia
                [ ]Institute of Cell Biology, NAS of Ukraine, 14-16 Drahomanov Str., 79005 Lviv, Ukraine
                [ ]Technical University of Ilmenau, Institute of Chemistry and Biotechnology, 25 Weimarer Str., 98693 Ilmenau, Germany
                Article
                1206
                10.1186/s11671-015-1206-7
                4695471
                26714861
                6e196f09-0969-4f51-8bc5-09178b4d18ad
                © Prylutska et al. 2015

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 17 November 2015
                : 16 December 2015
                Categories
                Nano Express
                Custom metadata
                © The Author(s) 2015

                Nanomaterials
                c60 fullerene,doxorubicin,antitumor effect,antimetastatic effect,immune response
                Nanomaterials
                c60 fullerene, doxorubicin, antitumor effect, antimetastatic effect, immune response

                Comments

                Comment on this article