Please note: In order to keep Hive up to date and provide users with the best features, we are no longer able to fully support Internet Explorer. The site is still available to you, however some sections of the site may appear broken. We would encourage you to move to a more modern browser like Firefox, Edge or Chrome in order to experience the site fully.

EGFR Signaling Networks in Cancer Therapy, Hardback Book

EGFR Signaling Networks in Cancer Therapy Hardback

Edited by John D. Haley, William John Gullick

Part of the Cancer Drug Discovery and Development series

Hardback

Description

The epidermal gro wth factor (EGF ) receptor and its downstream signal transduction networks have been implicated in the ontology and maintenance of tumor tissues, which has motivated the discovery and development of molecularly targeted anti-EGF receptor therapies.

Over decades of study, the EGF receptor structure, its ligand binding domains, the physical biochemistry underlying its intrinsic tyrosine kinase catalytic function and the modular interactions with SH2, PTB, and SH3 domain containing signaling adaptor p- teins required for signal transduction, have been extensively dissected.

Not only is the EGF receptor the nexus of many streams of information, but it also forms one part of a calcul- ing device by forming dimers and oligomers with the other three receptors in its family in response to at least eleven ligands (some of which are expressed in multiple forms with overlapping or quite distinct functions).

This phenomenon, while recruiting to the inner surface of the cell membrane and activating multiple second messenger proteins, also allows the possibility of cross talk between these systems, permitting a further layer of information to be exchanged.

Less well described are the cross re gulation of the EGF receptor and other anti-apoptotic, mitogenic and metabolic signaling systems.

The study of these systems has yielded new surprises.

One hurdle in these efforts has been that signal transduction pathways have frequently been defined in the generic absence of their tissue-specific or cell-interaction specific context.

Information

  • Format:Hardback
  • Pages:395 pages, 3 Tables, black and white; XI, 395 p.
  • Publisher:Humana Press Inc.
  • Publication Date:
  • Category:
  • ISBN:9781588299482
Save 14%

£199.99

£171.75

Item not Available
 
Free Home Delivery

on all orders

 
Pick up orders

from local bookshops

Information

  • Format:Hardback
  • Pages:395 pages, 3 Tables, black and white; XI, 395 p.
  • Publisher:Humana Press Inc.
  • Publication Date:
  • Category:
  • ISBN:9781588299482