Targeted induction of apoptosis for cancer therapy: current progress and prospects

Edwin Bremer1, Go van Dam, Bart Jan Kroesen

  • 1Groningen University Institute for Drug Exploration (GUIDE), Department of Pathology and Laboratory Medicine, Section Medical Biology, Laboratory for Tumor Immunology, University Medical Center Groningen, University of Groningen, The Netherlands.

Insights

Novel cancer therapies selectively induce apoptosis in malignant cells, overcoming resistance. This approach targets cancer-specific vulnerabilities for effective treatment with minimal harm to normal cells.

Area of Science:

  • Oncology
  • Molecular Biology
  • Drug Discovery

Background:

  • Current cancer therapies like antibodies (Rituximab) and small molecules (Iressa, Velcade) show success.
  • Physiological pro-apoptotic proteins (TRAIL, galectin-1) also demonstrate therapeutic potential.
  • Cancer therapy resistance is often linked to dysregulated apoptosis mechanisms.

Purpose of the Study:

  • To review novel anti-cancer strategies.
  • To highlight approaches that selectively induce apoptosis in cancer cells.
  • To discuss prospects of targeting cancer cell apoptosis.

Main Methods:

  • Review of recent scientific literature.
  • Analysis of therapeutic strategies targeting apoptosis.
  • Evaluation of novel anti-cancer agents.

Main Results:

  • Selected novel approaches deliberately and selectively induce apoptosis in malignant cells.
  • Cancer cells' reliance on aberrant apoptosis pathways presents a therapeutic vulnerability.
  • Selective apoptosis induction in cancer cells, sparing normal cells, appears feasible.

Conclusions:

  • Targeting and sensitizing cancer cells to apoptosis represents a promising therapeutic avenue.
  • Novel strategies focus on exploiting cancer-specific apoptosis dysregulation.
  • Further research into these selective apoptosis-inducing agents is warranted for future cancer treatment.

Related Concept Videos

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...
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...
Combination Therapies and Personalized Medicine02:50

Combination Therapies and Personalized Medicine

Combining two or more treatment methods increases the life span of cancer patients while reducing damage to vital organs or tissue from the overuse of a single treatment. Combination therapy also targets different cancer-inducing pathways, thus reducing the chances of developing resistance to treatment.
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
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...