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Epigenetic Regulation01:37

Epigenetic Regulation

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Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
X-chromosome...
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Induced Pluripotent Stem Cells01:06

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Stem cells are undifferentiated cells that divide and produce different cell types. Ordinarily, cells that have differentiated into a specific cell type are terminally differentiated; however, scientists have found a way to reprogram these mature cells so that they dedifferentiate and return to an unspecialized, proliferative state. These cells are pluripotent like embryonic stem cells—able to produce all cell types—and are called induced pluripotent stem cells (iPSCs).
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Adaptive Mechanisms in Cancer Cells02:53

Adaptive Mechanisms in Cancer Cells

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Cancer cells accumulate genetic changes at an abnormally rapid rate due to the defects in the DNA repair mechanisms. From an evolutionary perspective, such genetic instability is advantageous for cancer development. Mutant cell lines accumulate a series of beneficial mutations that contribute to their progression into cancer.
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
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mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

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The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
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Cancer-Critical Genes I: Proto-oncogenes01:33

Cancer-Critical Genes I: Proto-oncogenes

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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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Abnormal Proliferation02:23

Abnormal Proliferation

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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...
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Related Experiment Video

Updated: May 30, 2025

Investigation of the Transcriptional Role of a RUNX1 Intronic Silencer by CRISPR/Cas9 Ribonucleoprotein in Acute Myeloid Leukemia Cells
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Enhancer-dependent gene regulation in space, time, and malignancies.

Belinda Blum1,2, Victoria Dachtler1,2, Angelika Feldmann1,2

  • 1Mechanisms of Genome Control, German Cancer Research Center (DKFZ), Heidelberg, Germany.

International Journal of Cancer
|January 31, 2025
PubMed
Summary

Enhancers control gene activation through temporal integration. Aberrant enhancer activity, including epigenetic changes, drives cancer development, highlighting their critical role in cell regulation.

Keywords:
cancer epigeneticsdistal regulatory elementsenhancer hijackinggenome structuretemporal dynamics

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Area of Science:

  • Molecular Biology
  • Genetics
  • Epigenetics

Background:

  • Cell-type-specific gene activation relies on coordinated distal regulatory elements like enhancers.
  • Enhancer function requires temporal integration of regulatory inputs.
  • Dysregulation of enhancers can lead to cellular malignant transformation.

Purpose of the Study:

  • To review current understanding of enhancer-driven gene regulation.
  • To discuss temporal integration of enhancer activity.
  • To explore epigenetic and structural alterations of enhancers in cancer.

Main Methods:

  • Literature review of enhancer function and regulation.
  • Analysis of temporal integration mechanisms in gene activation.
  • Examination of epigenetic modifications and structural changes in cancer enhancers.

Main Results:

  • Enhancers integrate regulatory signals over time for precise gene control.
  • Aberrant enhancer usage and alterations are linked to cancer.
  • Epigenetic and structural changes in enhancers contribute to oncogenesis.

Conclusions:

  • Understanding enhancer dynamics is crucial for comprehending normal cell function and disease.
  • Targeting enhancer dysregulation presents potential therapeutic strategies for cancer.
  • Further research into enhancer regulation and its role in cancer is warranted.