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Related Concept Videos

Cancer-Critical Genes II: Tumor Suppressor Genes01:05

Cancer-Critical Genes II: Tumor Suppressor Genes

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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.
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The Retinoblastoma Gene01:20

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Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
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Cancer-Critical Genes I: Proto-oncogenes01:33

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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.
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Immune evasion in locally advanced mismatch repair-deficient microsatellite instability-high colorectal cancer: Reduced T-cell infiltration and upregulation of epithelial IDO1 expression.

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[Hereditary cancer predisposition syndromes-significance of gynecological cancers].

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Related Experiment Video

Updated: May 7, 2026

A Genetically Engineered Mouse Model of Sporadic Colorectal Cancer
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[Hereditary colorectal cancer].

Hendrik Bläker1, Anne Kathrin Höhn2

  • 1Institut für Pathologie, Universitätsklinikum Leipzig AöR, Liebigstraße 26, 04103, Leipzig, Deutschland. hendrik.blaeker@medizin.uni-leipzig.de.

Pathologie (Heidelberg, Germany)
|May 5, 2026
PubMed
Summary

Hereditary colorectal cancer is linked to gene mutations, but some conditions like serrated polyposis lack clear genetic causes. Pathologists play a key role in diagnosing hereditary cancer and recommending genetic counseling.

Area of Science:

  • Oncology
  • Genetics
  • Pathology
Keywords:
CarcinogenesisDNA mismatch repairGerm cellsHereditary nonpolyposis colorectal neoplasmsProto-oncogene proteins B‑raf

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