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Related Concept Videos

Tumor Immunotherapy01:27

Tumor Immunotherapy

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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.
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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...
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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.
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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...
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Programmed death-1 & its ligands: promising targets for cancer immunotherapy.

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Novel cancer immunotherapies targeting the programmed death-1 (PD-1) pathway show promise. Combining PD-1 inhibitors with other treatments may enhance antitumor activity and overcome immune evasion in cancer.

Keywords:
PD-1 receptorPD-L1PD-ligandscombination cancer immunotherapyimmune escapeimmune inhibitory pathway

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Area of Science:

  • Immunology
  • Oncology
  • Cancer Research

Background:

  • Tumor immune evasion is a major challenge in cancer treatment.
  • Immune checkpoint inhibitors, particularly targeting the programmed death-1 (PD-1) pathway, have emerged as a promising strategy.
  • Anti-PD-1 antibodies like pembrolizumab and nivolumab are approved for advanced melanoma.

Purpose of the Study:

  • To review novel strategies for cancer immunotherapy.
  • To discuss the combination of PD-1/PD-ligand inhibitors with other therapies.
  • To explore methods for overcoming immune tolerance and enhancing antitumor responses.

Main Methods:

  • Literature review of preclinical and clinical studies on PD-1 pathway blockade.
  • Analysis of combination strategies involving immune checkpoint modulators and standard-of-care therapies.
  • Discussion of research on breaking immune tolerance in cancer.

Main Results:

  • Preclinical and clinical data support the efficacy of PD-1 pathway blockade.
  • Approved anti-PD-1 therapies demonstrate success in specific melanoma cases.
  • Combining PD-1 inhibitors with other agents is a key area of ongoing research.

Conclusions:

  • The PD-1/PD-ligand pathway is a critical target for cancer immunotherapy.
  • Combination therapies hold potential for increasing efficacy and broadening applicability.
  • Further research is crucial to optimize strategies for potent antitumor activity.