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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...
Inhibition of Cdk Activity02:34

Inhibition of Cdk Activity

The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
Abnormal Proliferation02:23

Abnormal Proliferation

Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the daughter...
Cancer-Critical Genes II: Tumor Suppressor Genes01:05

Cancer-Critical Genes II: Tumor Suppressor Genes

Genes usually encode proteins necessary for the proper functioning of a healthy cell. Mutations can often cause changes to the gene expression pattern, thereby altering the phenotype.
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...
Cancer-Critical Genes II: Tumor Suppressor Genes01:05

Cancer-Critical Genes II: Tumor Suppressor Genes

Genes usually encode proteins necessary for the proper functioning of a healthy cell. Mutations can often cause changes to the gene expression pattern, thereby altering the phenotype.
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...

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Related Experiment Video

Updated: May 13, 2026

Through the Looking Glass: Time-lapse Microscopy and Longitudinal Tracking of Single Cells to Study Anti-cancer Therapeutics
06:00

Through the Looking Glass: Time-lapse Microscopy and Longitudinal Tracking of Single Cells to Study Anti-cancer Therapeutics

Published on: May 14, 2016

Siah: a promising anticancer target.

Christina S F Wong1, Andreas Möller

  • 1Tumour Microenvironment Laboratory, Queensland Institute of Medical Research, Herston, Queensland, Australia.

Cancer Research
|March 5, 2013
PubMed
Summary
This summary is machine-generated.

Siah ubiquitin ligases have complex roles in cancer progression, acting as both oncogenes and tumor suppressors. Further research is needed to clarify their function and therapeutic potential in cancer treatment.

Related Experiment Videos

Last Updated: May 13, 2026

Through the Looking Glass: Time-lapse Microscopy and Longitudinal Tracking of Single Cells to Study Anti-cancer Therapeutics
06:00

Through the Looking Glass: Time-lapse Microscopy and Longitudinal Tracking of Single Cells to Study Anti-cancer Therapeutics

Published on: May 14, 2016

Area of Science:

  • Oncology
  • Molecular Biology
  • Biochemistry

Background:

  • Siah ubiquitin ligases are implicated in cancer signaling pathways.
  • Their role in tumor progression is debated, with evidence suggesting both oncogenic and tumor-suppressive functions.
  • Contradictory findings exist across cell models, patient cohorts, and animal studies.

Purpose of the Study:

  • To review current knowledge on Siah proteins in cancer progression.
  • To identify potential clinical applications of Siah research.
  • To suggest critical experiments to resolve ambiguities in Siah's role.

Main Methods:

  • Literature review and synthesis of existing research on Siah ubiquitin ligases in cancer.
  • Analysis of data from cell-based models, patient cohorts, and animal cancer models.
  • Identification of knowledge gaps and proposal of future experimental directions.

Main Results:

  • Siah proteins exhibit dual roles in cancer, acting as both promoters and inhibitors of tumor progression.
  • Evidence for Siah's function varies significantly depending on the cancer type and model system studied.
  • Current understanding is insufficient for direct clinical translation.

Conclusions:

  • The precise role of Siah ubiquitin ligases in cancer progression requires further elucidation.
  • Targeting Siah proteins may offer therapeutic opportunities, but requires a deeper understanding of their context-dependent functions.
  • Future research should focus on resolving conflicting data and defining Siah's specific contributions to tumorigenesis and metastasis.