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020 _a9783319127309
024 7 _a10.1007/978-3-319-12730-9
_2doi
040 _aES-MaUEC
050 4 _aRC271.P43
_bR475 2015
245 1 0 _aResistance to Photodynamic Therapy in Cancer
_cedited by Valentina Rapozzi, Giulio Jori.
260 _aCham, Switzerland
_bSpringer
_c2015
300 _a1 recurso en línea (XV, 248 páginas)
_b48 ilustraciones, 36 ilustraciones en color
336 _aTexto
_btxt
_2rdacontent
337 _aelectrónico
_bc
_2rdamedia
338 _arecurso electrónico
_bcr
_2rdacarrier
490 0 _aResistance to Targeted Anti-Cancer Therapeutics
_x2196-5501
_v5
505 0 _aBasic and Clinical Aspects of photodynamic Therapy -- Mechanisms of Resistance to Photodynamic Therapy -- Tumor Vascular Microenvironment Determines responsiveness to Photodynamic Therapy -- Autophagy Pathways Activated in Response to PDT Contribute to Cell Resistance Against ROS Damage -- Methods to isolate the Resistant Cells to Photodynamic Therapy -- GRP78-Targeting Subtilase Cytotoxin Sensitizes Cancer Cells to Photodynamic Therapy -- Optimization of Photodynamic Therapy Response by Survivin Gene Knockdown in Human Metastatic Breast Cancer -- Cellular Targets and Molecular Responses Associated with Photodynamic Therapy -- The Use of Nanoparticle-Delivered Photosensitizers Can Overcome the Development of Resistance to PDT in Tumors -- Mechanisms of tumor cells resistance to ALA/PDT -- Overcoming the Resistance of Meolanoma to Photodynamic Therapy.
520 3 _aThis volume provides a comprehensive review of resistance induced by photodynamic therapy (PDT) in tumor cells. Understanding the underlying mechanisms in this process leads to the improvement of therapeutic modality, in combination with chemotherapy, immunotherapy, and radiotherapy. Photodynamic therapy is a minimally invasive therapeutic procedure that can exert a selective or preferential cytotoxic activity toward malignant cells. The procedure involves administration of an intrinsically non-toxic photosensitizing agent (PS) followed by irradiation at a wavelength corresponding to a visible absorption band of the sensitizer. In the presence of oxygen, a series of events lead to direct tumor cell death, damage to the microvasculature, and induction of a local inflammatory reaction. Studies reveal that PDT can be curative, particularly in early stage tumors and this volume explores the potential of PDT, but also reveals strategic approaches to overcome resistance in tumor cells.
650 7 _aResistencia a los medicamentos
_2embne
_9146972
650 7 _aBiología molecular
_2embne
_9139103
650 2 7 _aBiología molecular
_2embne
_9139103
700 1 _aRapozzi, Valentina
_eeditor literario
_993652
_0Local
700 1 _aJori, Giulio
_eeditor literario
_993653
_0Local
856 4 0 _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://link.springer.com/book/10.1007/978-3-319-12730-9
_zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
907 _a.b12898934
_b10-10-17
_c18-01-16
942 _2lcc
_cLE
945 _aRC271.P43 R475 2015 EB
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