New PDF release: Cancer Chemotherapy: Basic Science to the Clinic

By Rachel Airley

ISBN-10: 0470092548

ISBN-13: 9780470092545

ISBN-10: 0470092556

ISBN-13: 9780470092552

This textbook is a transparent and available creation to the medical and scientific elements of the construction, improvement and management of gear or drug regimens utilized in the therapy of melanoma. certain in its strategy, this e-book permits the coed to achieve an realizing of the pathological, physiological and molecular procedures governing malignancy, while additionally introducing the position of wellbeing and fitness pros and scientists within the study and therapy of melanoma. The ebook consolidates all of the crucial info helpful for an entire knowing of melanoma chemotherapy, offering an informative, reasonably cheap and updated insurance of the topic geared toward an undergraduate point readership.

Key Features:

  • Incorporates quite a few diagrams, tables and illustrations to assist understanding.
  • Examines key pharmacological and pharmaceutical matters akin to dosing, toxicity and coaching of anti-cancer drugs.
  • Includes a key bankruptcy of perform essay inquiries to ease revision.
  • Comprehensive insurance of gear presently in pre-clinical and scientific development.
  • An crucial textual content for undergraduate scholars learning pharmacy and drugs in addition to these doing classes corresponding to molecular biology, biomedical sciences and pharmacology which hide facets of oncology.

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Extra info for Cancer Chemotherapy: Basic Science to the Clinic

Example text

Adapted from Miles et al. (2008) Clin. Exp. Metastasis 25:305–24. 1 Cancer dormancy Cancer dormancy describes the latent period between remission and the clinical diagnosis of relapse. Tumour recurrences are thought to be a consequence of minimal residual disease, where small undetectable numbers of tumour cells remain after treatment. Although these tumour cells persist within the patient, they do not have any clinical effects until, under certain circumstances, they are ‘activated’, leading to recurrences sometimes years later.

Tumour cells initially must detach from the primary tumour mass and invade into the blood or lymph vessels, to be transported as micrometastases. Detachment itself depends upon the extent of cell Cancer Chemotherapy Rachel Airley Ó 2009 John Wiley & Sons, Ltd. 38 CH 5 TUMOUR METASTASIS: A CONVERGENCE OF MANY THEORIES adherence, brought about by plasma membrane-bound cell adhesion molecules (CAMs) that are expressed by specific cell types within the tumour mass, such as: the integrins, for example, fibronectin, collagen; the cadherins, for example, E-cadherin; the selectins, for example, P- and E-selectins; and the connexins, which are involved with the formation of gap junctions between cells.

Mol. Med. 2008;86:523–9, Springer. following the ingress of water at the leading edge of the cell. Water is transported into cells by tissue-specific water channels, or aquaporins (AQPs). There are several isoforms, such as AQP1, expressed on endothelial cells, AQP3, found in skin neoplasms, and AQP4, in astrocytes within the brain. The process is initiated by the polarisation of cells under chemotaxis, forming leading and retracting edges. Actin depolymerization is accompanied by the movement of ions into the front end of the cell due to the activity of Na þ /H þ and ClÀ/HCO3À ion exchange channels.

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Cancer Chemotherapy: Basic Science to the Clinic by Rachel Airley

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