Apoptosis in human primary brain tumours

H A Leaver1, I R Whittle, S B Wharton

  • 1Department of Pharmacology, Edinburgh University, UK. pengl a netcomuk.co.uk

Insights

Apoptosis, programmed cell death, is fundamental to human brain tumors like gliomas. Understanding its pathways and analyzing apoptosis methods are key for developing new glioma therapies.

Area of Science:

  • Cell Biology
  • Neuro-Oncology
  • Molecular Biology

Background:

  • Apoptosis, or programmed cell death, is a fundamental biological process observed in various organs under pathophysiological conditions.
  • Initially termed 'shrinkage necrosis' in human gliomas, apoptosis is crucial for understanding tumor development.
  • This review focuses on apoptosis in primary human brain tumors, particularly gliomas.

Purpose of the Study:

  • To outline the characteristics of apoptosis in different types of primary human brain tumors.
  • To review the significance of apoptosis in normal and tumor cell dynamics and susceptibility to signals.
  • To discuss potential therapeutic advances, including pro-apoptotic therapy for gliomas.

Main Methods:

  • Review of existing literature on apoptosis in human brain tumors.
  • Critical evaluation and comparison of current methods for analyzing apoptosis.
  • Discussion of current developments in elucidating apoptosis signaling pathways.

Main Results:

  • Apoptosis plays a significant role in the dynamics of normal and tumor cells.
  • Understanding apoptosis is crucial for assessing cellular susceptibility to oncogenic signals.
  • Various methods exist for analyzing apoptosis, each with its own strengths and limitations.

Conclusions:

  • Apoptosis is a critical process in human brain tumors, influencing tumor cell dynamics and therapeutic responses.
  • Analysis of apoptosis and its signaling pathways provides insights into tumor biology.
  • Pro-apoptotic therapies hold potential for the future treatment of gliomas.

Related Concept Videos

Apoptosis01:30

Apoptosis

Apoptosis is a combination of two Greek words, 'apo' and 'ptosis,' meaning separation and falling off, respectively. Hippocrates used this word to describe gangrene, which was caused due to bandaging of fractured bones. Apoptosis was distinguished from necrosis in 1970 when John Kerr reported observations of morphological changes occurring during apoptosis. During one experiment, he observed that the disruption of blood supply to the liver tissue resulted in a size reduction of the tissue.
The Intrinsic Apoptotic Pathway01:31

The Intrinsic Apoptotic Pathway

Internal cellular stress, such as cellular injury or hypoxia, triggers intrinsic apoptosis. The B-cell lymphoma 2 (Bcl-2) family of proteins are the primary regulators of the intrinsic apoptotic pathway. For example, during DNA damage, checkpoint proteins, such as Ataxia Telangiectasia Mutated (ATM protein) and Checkpoints Factor-2 (Chk2) proteins, are activated. These proteins phosphorylate p53 which further activates pro-apoptotic proteins, such as Bax, Bak, PUMA, and Noxa, and inhibits...
Phagocytosis of Apoptotic Cells01:17

Phagocytosis of Apoptotic Cells

Cells undergoing apoptosis form apoptotic bodies that must be removed immediately to prevent inflammation, autoimmune diseases, and necrosis. Phagocytosis is carried out by professional phagocytes such as macrophages or  immature dendritic cells. Non-professional phagocytes such as  epithelial cells and fibroblasts also take part in this process; however, they are not as effective as professional phagocytes. 
Normal cells contain receptors that prevent them from being recognized by phagocytes.