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Novel Anti-cancer Agents and Cellular Targets and Their Mechanism(s) of Action

Novel Anti-cancer Agents and Cellular Targets and Their Mechanism(s) of Action

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Patient outcomes remain poor for many cancers despite improvements in treatments and new molecular-targeted biomedicines for certain cancer types or subtypes. Dose-limiting toxicity, a narrow therapeutic index, and the development of resistance to traditional anti-cancer agents are well-established. It is apparent that inherent and acquired drug resistance are major challenges with molecular-targeted agents and that on- as well as off-target side effects can still occur. Other issues include drug metabolism by the body and safely supplying a sufficient amount of active drug to the tumor cells. There is a clear and urgent need for new molecular targets and drugs that specifically target cancer cells in different ways to existing approved drugs. This book, through a collection of eight research articles and two review articles from the Biomedicines themed Special Issue ‘Novel Anti-Cancer Agents and Cellular Targets and Their Mechanism(s) of Action’, provides a snapshot of some of the diverse and exciting research approaches being taken by the cancer research community in trying to address some of these therapeutic challenges.

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Keywords

  • 5-FU resistance
  • 8-hydroxydaidzein
  • affibody drug conjugate (AffiDC)
  • affibody molecule
  • albumin binding domain
  • Angiogenesis
  • anti-cancer agent
  • anticancer drug
  • Apoptosis
  • AQ4N
  • Autophagy
  • B-lactam steroid alkylators
  • BCR-ABL
  • biomarker
  • bioprecursor
  • Breast cancer
  • BxPC-3
  • c-myc
  • cancer hallmarks
  • CCN1
  • colorectal cancer
  • Connectivity Map
  • CYP1A1
  • CYP1B1
  • CYP2W1
  • Cytochrome P450
  • DM1
  • drug repurposing
  • duocarmycin
  • EGFR tyrosine kinase inhibitor
  • emtansine
  • Expression
  • Gene silencing
  • Genomics of Drug Sensitivity in Cancer
  • Glioblastoma
  • HepG2
  • History of engineering & technology
  • Huh7
  • human epidermal growth factor receptor 3 (HER3)
  • hybrid steroidal alkylating agents
  • in vivo imaging
  • Invasion
  • isatin sulfonamides
  • K562
  • MAPK
  • mesenchymal–amoeboid transition
  • microtubule acetylation
  • migration
  • molecular docking
  • n/a
  • Nanoparticles
  • nanosystems
  • NF-κB
  • oncogene
  • ovarian cancer
  • phortress
  • photon upconversion
  • PLGA
  • poly (ADP-ribose) polymerase inhibitors
  • prodrug
  • RNA interference
  • siRNA
  • synthetic lethality
  • Technology, engineering, agriculture
  • Technology: general issues
  • triple-negative breast cancer
  • triplet-triplet annihilation

Links

DOI: 10.3390/books978-3-0365-5222-4

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