Tumor cell-selective apoptosis induction through targeting of K(V)10.1 via bifunctional TRAIL antibody

Franziska Hartung1, Walter Stühmer, Luis A Pardo

  • 1Max-Planck-Institut für Experimentelle Medizin, Hermann-Rein-Str, 3, 37075 Göttingen, Germany.

Molecular Cancer
|September 9, 2011
PubMed
Abstract

Insights

Researchers developed a novel antibody-TRAIL fusion protein targeting the K(V)10.1 ion channel. This strategy selectively induces apoptosis in K(V)10.1-positive cancer cells, sparing normal tissues and offering a promising new cancer therapy.

Area of Science:

  • Oncology
  • Molecular Biology
  • Immunotherapy

Background:

  • The K(V)10.1 ion channel is a potential therapeutic target due to its restricted expression in normal tissues but high prevalence in various cancers.
  • Targeting ion channels offers a promising avenue for novel cancer therapies.

Purpose of the Study:

  • To develop and evaluate a novel therapeutic strategy targeting the K(V)10.1 ion channel for cancer treatment.
  • To assess the selective killing of K(V)10.1-expressing tumor cells using a targeted fusion protein.

Main Methods:

  • A single-chain antibody (scFv62) targeting an extracellular K(V)10.1 region was engineered.
  • The antibody was fused to human soluble TRAIL (scFv62-TRAIL) and expressed in CHO-K1 cells.
  • The purified fusion protein's biological activity was tested on cancer cells and normal cells.

Main Results:

  • The scFv62-TRAIL fusion protein selectively induced apoptosis in K(V)10.1-positive cancer cells, including bystander cells.
  • No significant toxicity was observed in non-tumor cells or K(V)10.1-negative tumor cells.
  • Normal prostate epithelial cells were unaffected when present as bystanders.

Conclusions:

  • K(V)10.1 is a viable and novel therapeutic target for various cancers.
  • A K(V)10.1-specific antibody-based strategy can effectively and selectively eliminate tumor cells.

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...
Tumor Immunotherapy01:27

Tumor Immunotherapy

Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
Cytotoxic T Cells-mediated Immune Response01:27

Cytotoxic T Cells-mediated Immune Response

Cytotoxic T cells are a vital component of the immune system. They have the remarkable ability to identify and target antigens on infected or abnormal cells. These antigens often originate from intracellular pathogens such as viruses or abnormal proteins cancer cells produce.
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...
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...
The Extrinsic Apoptotic Pathway01:17

The Extrinsic Apoptotic Pathway

The extrinsic apoptotic pathway is initiated when extracellular death-inducing signals, such as specific cytokines, activate the death receptors expressed on the cell surface. The immune cells involved in this pathway are natural killer cells (NK cells) and cytotoxic T-lymphocytes. NK cells are critical in innate immune response, while cytotoxic T-lymphocytes are associated with adaptive immune response. These cells recognize specific receptors expressed on the altered cells and activate...
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...