Angiogenesis in the treatment of non-small cell lung cancer

Leora Horn1, Alan B Sandler

  • 1Vanderbilt Ingram Cancer Center, Vanderbilt University, Nashville, TN 32323-6307, USA.

Insights

Antiangiogenic agents, like bevacizumab targeting vascular endothelial growth factor (VEGF), show promise in improving survival for advanced non-small cell lung cancer (NSCLC) when combined with chemotherapy.

Area of Science:

  • Oncology
  • Cancer Biology
  • Pharmacology

Background:

  • Lung cancer is a leading cause of cancer mortality.
  • Advanced non-small cell lung cancer (NSCLC) has limited survival with standard chemotherapy.
  • Angiogenesis is crucial for tumor growth and progression.

Purpose of the Study:

  • To review clinical trials of antiangiogenic agents in NSCLC treatment.
  • To evaluate the role of novel targeted therapies in NSCLC.

Main Methods:

  • Review of clinical trials incorporating antiangiogenic agents.
  • Analysis of bevacizumab combination therapy in NSCLC.
  • Assessment of small molecule inhibitors targeting VEGF and tyrosine kinase receptors.

Main Results:

  • Bevacizumab combined with chemotherapy improved overall survival in advanced NSCLC.
  • Small molecule inhibitors show potential but require further investigation.

Conclusions:

  • Antiangiogenic therapy, particularly bevacizumab, offers a survival benefit in advanced NSCLC.
  • Targeted antiangiogenic agents represent a promising strategy for NSCLC treatment.

Related Concept Videos

Mechanism of Angiogenesis01:10

Mechanism of Angiogenesis

Blood vessel formation starts early during embryonic development, around day 7. In the extraembryonic yolk sac, mesodermal precursor cells called hemangioblast proliferate and differentiate into angioblast. Angioblasts express vascular endothelial growth factor receptor 2 or VEGFR2, which binds VEGF-A, a proangiogenic factor, guiding blood vessel formation. VEGF signaling promotes angioblasts to form a blood island in the developing embryo. Angioblasts further differentiate, giving rise to...
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against specific...
Cancer Therapies02:49

Cancer Therapies

Cancer therapies are various modes of treatment, such as surgery, radiation therapy, and chemotherapy that are administered to cancer patients.
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
Regulation of Angiogenesis and Blood Supply01:24

Regulation of Angiogenesis and Blood Supply

Rapidly dividing tumors, embryos, and wounded tissues require more oxygen than usual, lowering the oxygen concentration in the blood. At low oxygen or hypoxic conditions, an oxygen-sensitive transcription factor called the hypoxia-inducible factor 1 or HIF1 is activated. HIF1 is a dimeric protein of alpha (ɑ) and beta (β) subunits.  Under optimal oxygen conditions, HIF1β is present in the nucleus while HIF1ɑ remains in the cytosol. HIF1ɑ is hydroxylated by prolyl hydroxylase and factor...