We use cookies to distinguish you from other users and to provide you with a better experience on our websites. Close this message to accept cookies or find out how to manage your cookie settings.
To save content items to your account,
please confirm that you agree to abide by our usage policies.
If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account.
Find out more about saving content to .
To save content items to your Kindle, first ensure no-reply@cambridge.org
is added to your Approved Personal Document E-mail List under your Personal Document Settings
on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part
of your Kindle email address below.
Find out more about saving to your Kindle.
Note you can select to save to either the @free.kindle.com or @kindle.com variations.
‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi.
‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.
from
SECTION 3
-
IMAGING AND THERAPY: STATE OF THE ART
By
Ahmed Ashour Ahmed, University of Oxford,
Stefan Knapp, Nuffield Department of Clinical Medicine,
Anil K Sood, The University of Texas MD Anderson Cancer Center,
Robert C Bast, The University of Texas MD Anderson Cancer Center
This chapter outlines the recent advances in the molecular classification of ovarian cancer and the efforts for rationalised targeted therapies of molecular drivers of individual cancers with a particular emphasis on kinases and their inhibitors. It highlights the challenges that face targeting strategies, particularly at the interface between target discovery and validation that leads to the development of targeting agents. Development of small interfering RNA (siRNA) technology could provide a tool to overcome the shortcomings of some current therapeutic approaches. One of the challenges surrounding the use of siRNA for systemic therapy relates to the need for efficient and biocompatible delivery vehicles. Liposomes, in general, have been shown to be safe in a number of clinical trials using a wide variety of anti-cancer and antimicrobial drugs. Chitosan nanoparticles are highly effective for delivery of siRNA into both tumour and tumour-associated endothelial cells.
Recommend this
Email your librarian or administrator to recommend adding this to your organisation's collection.