全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Stem Cells as a Tool for Breast Imaging

DOI: 10.1155/2012/814014

Full-Text   Cite this paper   Add to My Lib

Abstract:

Stem cells are a scientific field of interest due to their therapeutic potential. There are different groups, depending on the differentiation state. We can find lonely stem cells, but generally they distribute in niches. Stem cells don’t survive forever. They are affected for senescence. Cancer stem cells are best defined functionally, as a subpopulation of tumor cells that can enrich for tumorigenic property and can regenerate heterogeneity of the original tumor. Circulating tumor cells are cells that have detached from a primary tumor and circulate in the bloodstream. They may constitute seeds for subsequent growth of additional tumors (metastasis) in different tissues. Advances in molecular imaging have allowed a deeper understanding of the in vivo behavior of stem cells and have proven to be indispensable in preclinical and clinical studies. One of the first imaging modalities for monitoring pluripotent stem cells in vivo, magnetic resonance imaging (MRI) offers high spatial and temporal resolution to obtain detailed morphological and functional information. Advantages of radioscintigraphic techniques include their picomolar sensitivity, good tissue penetration, and translation to clinical applications. Radionuclide imaging is the sole direct labeling technique used thus far in human studies, involving both autologous bone marrow derived and peripheral stem cells. 1. Stem Cells Stem cells are a scientific field of interest mainly due to their therapeutic potential. The term of stem cells came up to us via histologists in the nineteenth century, who introduced it as a general, abstract term for cells specifically involved in repair or regeneration. With the discovery in the 1950s that bone marrow cells could reconstitute the hematopoietic systems of irradiated individuals, the modern stem cell concept began to crystallize around the experimental procedures of transplantation and reconstitution [1, 2]. The definition for tissue stem cells proposed by Potten and Loeffler was undifferentiated cells (relative to a functional tissue), capable of proliferation and production of a large number of differentiated functional progeny; they have the ability of self-maintenance of their population and for regeneration of the tissue after injury. This means that stem cells are defined by virtue of their functional attributes and not by an explicit directly observable characteristic. This functional definition is relative to the stem cell role linked to the functional tissue regeneration feature. But this definition doesn’t give us any characteristic to identify

References

[1]  C. S. Potten and M. Loeffler, “Stem cells: attributes, cycles, spirals, pitfalls and uncertainties. Lessons for and from the crypt,” Development, vol. 110, no. 4, pp. 1001–1020, 1990.
[2]  M. Loeffler and C. S. Potten, “Stem cells and cellular pedigrees a conceptual introduction,” in Stem Cells, C. S. Potten, Ed., pp. 1–28, Harcourt Brace and Company, San Diego, Calif, USA, 1997.
[3]  M. Loeffler and I. Roeder, “Tissue stem cells: definition, plasticity, heterogeneity, self-organization and models—a conceptual approach,” Cells Tissues Organs, vol. 171, no. 1, pp. 8–26, 2002.
[4]  S. Mitalipov and D. Wolf, “Totipotency, pluripotency and nuclear reprogramming,” Advances in Biochemical Engineering/Biotechnology, vol. 114, pp. 185–199, 2009.
[5]  D. T. Scadden, “The stem-cell niche as an entity of action,” Nature, vol. 441, no. 7097, pp. 1075–1079, 2006.
[6]  J. A. Knoblich, “Mechanisms of asymmetric stem cell division,” Cell, vol. 132, no. 4, pp. 583–597, 2008.
[7]  P. Anversa, “Aging and longevity: the IGF-1 enigma,” Circulation Research, vol. 97, no. 5, pp. 411–414, 2005.
[8]  M. Rota, N. LeCapitaine, T. Hosoda et al., “Diabetes promotes cardiac stem cell aging and heart failure, which are prevented by deletion of the p66shc gene,” Circulation Research, vol. 99, no. 1, pp. 42–52, 2006.
[9]  A. D. Lander, “The “stem cell” concept: is it holding us back?” Journal of Biology, vol. 8, no. 8, article 70, 2009.
[10]  T. Brabletz, A. Jung, S. Spaderna, F. Hlubek, and T. Kirchner, “Migrating cancer stem cells—an integrated concept of malignant tumour progression,” Nature Reviews Cancer, vol. 5, no. 9, pp. 744–749, 2005.
[11]  J. Couzin, “Tracing the steps of metastasis, cancer's menacing ballet,” Science, vol. 299, no. 5609, pp. 1002–1006, 2003.
[12]  B. G. Hollier, K. Evans, and S. A. Mani, “The epithelial-to-mesenchymal transition and cancer stem cells: a coalition against cancer therapies,” Journal of Mammary Gland Biology and Neoplasia, vol. 14, no. 1, pp. 29–43, 2009.
[13]  I. J. Fidler, “The pathogenesis of cancer metastasis: the“seed and soil” hypothesis revisited,” Nature Reviews Cancer, vol. 3, no. 6, pp. 453–458, 2003.
[14]  A. da Costa, J. T. Oliveira, F. G?rtner, B. Kohn, A. D. Gruber, and R. Klopfleisch, “Potential markers for detection of circulating canine mammary tumor cells in the peripheral blood,” Veterinary Journal, vol. 190, no. 1, pp. 165–168, 2010.
[15]  R. A. Ghossein, S. Bhattacharya, and J. Rosai, “Molecular detection of micrometastases and circulating tumor cells in solid tumors,” Clinical Cancer Research, vol. 5, no. 8, pp. 1950–1960, 1999.
[16]  P. Paterlini-Brechot and N. L. Benali, “Circulating tumor cells (CTC) detection: clinical impact and future directions,” Cancer Letters, vol. 253, no. 2, pp. 180–204, 2007.
[17]  A. G. J. Tibbe, M. C. Miller, and L. W. M. M. Terstappen, “Statistical considerations for enumeration of circulating tumor cells,” Cytometry Part A, vol. 71, no. 3, pp. 154–162, 2007.
[18]  F. A. W. Coumans, C. J. M. Doggen, G. Attard, J. S. de Bono, and L. W. M. M. Terstappen, “All circulating EpCAM+CK+CD45-objects predict overall survival in castration-resistant prostate cancer,” Annals of Oncology, vol. 21, no. 9, pp. 1851–1857, 2010.
[19]  M. M. Welling, M. Duijvestein, A. Signore, and L. van der Weerd, “In vivo biodistribution of stem cells using molecular nuclear medicine imaging,” Journal of Cellular Physiology, vol. 226, no. 6, pp. 1444–1452, 2011.
[20]  Z. Li, Y. Suzuki, M. Huang et al., “Comparison of reporter gene and iron particle labeling for tracking fate of human embryonic stem cells and differentiated endothelial cells in living subjects,” Stem Cells, vol. 26, no. 4, pp. 864–873, 2008.
[21]  I. Niculescu-Duvaz and C. J. Springer, “Introduction to the background, principles, and state of the art in suicide gene therapy,” Molecular Biotechnology, vol. 30, no. 1, pp. 71–88, 2005.
[22]  F. Cao, M. Drukker, S. Lin et al., “Molecular imaging of embryonic stem cell misbehavior and suicide gene ablation,” Cloning and Stem Cells, vol. 9, no. 1, pp. 107–117, 2007.
[23]  E. Sykova, P. Jendelova, and V. Herynek, “Magnetic resonance imaging of stem cell migration,” Methods in Molecular Biology, vol. 750, part 2, pp. 79–90, 2011.
[24]  J. A. Frank, B. R. Miller, A. S. Arbab et al., “Clinically applicable labeling of mammalian and stem cells by combining superparamagnetic iron oxides and transfection agents,” Radiology, vol. 228, no. 2, pp. 480–487, 2003.
[25]  D. L. Kraitchman, A. W. Heldman, E. Atalar et al., “In vivo magnetic resonance imaging of mesenchymal stem cells in myocardial infarction,” Circulation, vol. 107, no. 18, pp. 2290–2293, 2003.
[26]  P. W. So, T. Kalber, D. Hunt et al., “Efficient and rapid labeling of transplanted cell populations with superparamagnetic iron oxide nanoparticles using cell surface chemical biotinylation for in vivo monitoring by MRI,” Cell Transplantation, vol. 19, no. 4, pp. 419–429, 2010.
[27]  J. W. M. Bulte, A. S. Arbab, T. Douglas, and J. A. Frank, “Preparation of magnetically labeled cells for cell tracking by magnetic resonance imaging,” Methods in Enzymology, vol. 386, pp. 275–299, 2004.
[28]  J. W. M. Bulte and D. L. Kraitchman, “Iron oxide MR contrast agents for molecular and cellular imaging,” NMR in Biomedicine, vol. 17, no. 7, pp. 484–499, 2004.
[29]  R. Sch?fer, R. Kehlbach, M. Müller et al., “Labeling of human mesenchymal stromal cells with superparamagnetic iron oxide leads to a decrease in migration capacity and colony formation ability,” Cytotherapy, vol. 11, no. 1, pp. 68–78, 2009.
[30]  J. W. M. Bulte, T. Douglas, B. Witwer et al., “Magnetodendrimers allow endosomal magnetic labeling and in vivo tracking of stem cells,” Nature Biotechnology, vol. 19, no. 12, pp. 1141–1147, 2001.
[31]  M. Hoehn, E. Küstermann, J. Blunk et al., “Monitoring of implanted stem cell migration in vivo: a highly resolved in vivo magnetic resonance imaging investigation of experimental stroke in rat,” Proceedings of the National Academy of Sciences of the United States of America, vol. 99, no. 25, pp. 16267–16272, 2002.
[32]  L. C. Amado, A. P. Saliaris, K. H. Schuleri et al., “Cardiac repair with intramyocardial injection of allogeneic mesenchymal stem cells after myocardial infarction,” Proceedings of the National Academy of Sciences of the United States of America, vol. 102, no. 32, pp. 11474–11479, 2005.
[33]  M. Hofmann, K. C. Wollert, G. P. Meyer et al., “Monitoring of bone marrow cell homing into the infarcted human myocardium,” Circulation, vol. 111, no. 17, pp. 2198–2202, 2005.
[34]  W. J. Kang, H. J. Kang, H. S. Kim, J. K. Chung, M. C. Lee, and D. S. Lee, “Tissue distribution of 18F-FDG-labeled peripheral hematopoietic stem cells after intracoronary administration in patients with myocardial infarction,” Journal of Nuclear Medicine, vol. 47, no. 8, pp. 1295–1301, 2006.
[35]  V. Sch?chinger, A. Aicher, N. D?bert et al., “Pilot trial on determinants of progenitor cell recruitment to the infarcted human myocardium,” Circulation, vol. 118, no. 14, pp. 1425–1432, 2008.
[36]  C. Dedobbeleer, D. Blocklet, M. Toungouz et al., “Myocardial homing and coronary endothelial function after autologous blood CD34+ progenitor cells intracoronary injection in the chronic phase of myocardial infarction,” Journal of Cardiovascular Pharmacology, vol. 53, no. 6, pp. 480–485, 2009.
[37]  N. Adonai, K. N. Nguyen, J. Walsh et al., “Ex vivo cell labeling with 64Cu-pyruvaldehyde-bis(N4-methylthiosemicarbazone) for imaging cell trafficking in mice with positron-emission tomography,” Proceedings of the National Academy of Sciences of the United States of America, vol. 99, no. 5, pp. 3030–3035, 2002.
[38]  A. F. Tarantal, C. C. I. Lee, C. A. Batchelder, J. E. Christensen, D. Prater, and S. R. Cherry, “Radiolabeling and in vivo imaging of transplanted renal lineages differentiated from human embryonic stem cells in fetal rhesus monkeys,” Molecular Imaging and Biology, vol. 14, no. 2, pp. 197–204, 2012.
[39]  J. Huang, C. C. I. Lee, J. L. Sutcliffe, S. R. Cherry, and A. F. Tarantal, “Radiolabeling Rhesus monkey CD34+ hematopoietic and mesenchymal stem cells with 64Cu-pyruvaldehyde-bis(N4-methylthiosemicarbazone) for MicroPET imaging,” Molecular Imaging, vol. 7, no. 1, pp. 1–11, 2008.
[40]  D. L. Kraitchman, M. Tatsumi, W. D. Gilson et al., “Dynamic imaging of allogeneic mesenchymal stem cells trafficking to myocardial infarction,” Circulation, vol. 112, no. 10, pp. 1451–1461, 2005.
[41]  K. J. Blackwood, B. Lewden, R. G. Wells et al., “In vivo SPECT quantification of transplanted cell survival after engraftment using (111)In-tropolone in infarcted canine myocardium,” Journal of Nuclear Medicine, vol. 50, no. 6, pp. 927–935, 2009.
[42]  S. Lyngb?k, R. S. Ripa, M. Haack-S?rensen et al., “Serial in vivo imaging of the porcine heart after percutaneous, intramyocardially injected 111In-labeled human mesenchymal stromal cells,” International Journal of Cardiovascular Imaging, vol. 26, no. 3, pp. 273–284, 2010.
[43]  M. Kurpisz, R. Czepczyński, B. Grygielska et al., “Bone marrow stem cell imaging after intracoronary administration,” International Journal of Cardiology, vol. 121, no. 2, pp. 194–195, 2007.
[44]  V. Caveliers, G. de Keulenaer, H. Everaert et al., “In vivo visualization of 111In labeled CD133+ peripheral blood stem cells after intracoronary administration in patients with chronic ischemic heart disease,” Quarterly Journal of Nuclear Medicine and Molecular Imaging, vol. 51, no. 1, pp. 61–66, 2007.
[45]  K. Stojanov, E. F. de Vries, D. Hoekstra, A. van Waarde, R. A. Dierckx, and I. S. Zuhorn, “[18F]FDG labeling of neural stem cells for in vivo cell tracking with positron emission tomography: inhibition of tracer release by phloretin,” Molecular Imaging, vol. 11, no. 1, pp. 1–12, 2012.
[46]  U. Ben-David and N. Benvenisty, “The tumorigenicity of human embryonic and induced pluripotent stem cells,” Nature Reviews Cancer, vol. 11, no. 4, pp. 268–277, 2011.
[47]  N. G. Kooreman and J. C. Wu, “Tumorigenicity of pluripotent stem cells: biological insights from molecular imaging,” Journal of the Royal Society Interface, vol. 7, supplement 6, pp. S753–S763, 2010.
[48]  A. S. Lee, C. Tang, F. Cao et al., “Effects of cell number on teratoma formation by human embryonic stem cells,” Cell Cycle, vol. 8, no. 16, pp. 2608–2612, 2009.
[49]  K. R. Francis and L. Wei, “Human embryonic stem cell neural differentiation and enhanced cell survival promoted by hypoxic preconditioning,” Cell Death and Disease, vol. 1, no. 2, article e22, 2010.
[50]  R. M. Dwyer, J. Ryan, R. J. Havelin et al., “Mesenchymal stem cell-mediated delivery of the sodium iodide symporter supports radionuclide imaging and treatment of breast cancer,” Stem Cells, vol. 29, no. 7, pp. 1149–1157, 2011.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133