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Hedgehog Signaling Pathway02:33

Hedgehog Signaling Pathway

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The Hedgehog gene (Hh) was first discovered due to its control of the growth of disorganized, hair-like bristles phenotype in Drosophila, much like hedgehog spines. Hh plays a crucial role in the development of organs and the maintenance of homeostasis in both invertebrates and vertebrates. However, while Drosophila has only one Hh protein, mammals have multiple functional Hedgehog proteins - Sonic (Shh), Desert (Dhh), and Indian Hedgehog (Ihh). All of these homologous proteins have adapted to...
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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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Anaphase Promoting Complex00:50

Anaphase Promoting Complex

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The stepwise destruction of specific proteins is necessary for the progression and completion of the cell cycle. Such proteins are ubiquitinated by ubiquitin ligases and then subsequently destroyed by the proteasome. The SCF (Skp1/Cullin/F-box) and the anaphase-promoting complex (APC) are two important ubiquitin ligases involved in cell cycle progression. While SCF is active throughout the cell cycle, APC gets activated during metaphase to anaphase transition. Cdc20 or Cdh1 binds to APC and...
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TGF - β Signaling Pathway01:16

TGF - β Signaling Pathway

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The TGF-β signaling pathway regulates cell growth, differentiation, adhesion, motility, and development. TGF-β ligands that induce TGF-β signaling are synthesized in their latent form. Several proteases or cell surface receptors such as integrins act upon the latent form, releasing the active ligand. There are three types of mammalian TGF-βs: (TGF-β1, TGF-β2, and TGF-β3) that bind as homodimers or heterodimers to TGF-β receptors. The TGF-β receptors...
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Catenins01:23

Catenins

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Catenins are characterized by multiple binding domains and dynamic structures that allow them to function as linker proteins in cell junction complexes. All catenins, except α-catenin, contain a characteristic protein sequence called the armadillo repeat and are therefore also called armadillo proteins.
Catenins in Cell Junctions
Catenins bind to cell adhesion molecules such as cadherins and link them to different cytoskeletal proteins depending on the type of cell junction. At the...
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Cytoskeletal Accessory Proteins01:13

Cytoskeletal Accessory Proteins

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The cytoskeleton is an essential cell component that plays several structural and functional roles. However, the filaments that make up the cytoskeleton cannot function independently and depend on the accessory or ancillary proteins to effectively carry out their function. Accessory proteins associate with cytoskeletal filaments and their monomers, aiding filament formation and function. They also help in the cross-communication among cytoskeletal filaments. Cytoskeletal accessory proteins are...
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Related Experiment Video

Updated: Jan 6, 2026

A Mimic of the Tumor Microenvironment: A Simple Method for Generating Enriched Cell Populations and Investigating Intercellular Communication
09:52

A Mimic of the Tumor Microenvironment: A Simple Method for Generating Enriched Cell Populations and Investigating Intercellular Communication

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Bringing Oncohistones into the Fold.

Jay F Sarthy1,2, Steven Henikoff3,4

  • 1Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.

Cancer Discovery
|October 3, 2019
PubMed
Summary
This summary is machine-generated.

Identifying cancer-driving mutations in histone genes is difficult. New research shows histone fold mutations impact nucleosome stability, revealing a new way oncohistones promote cancer development.

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Area of Science:

  • Genomic medicine
  • Molecular oncology
  • Epigenetics

Background:

  • Core histone genes are highly conserved and present in large arrays, making mutation identification challenging.
  • Cancer-associated mutations in histone genes are increasingly recognized but their functional impact is not fully understood.
  • Understanding the role of histone mutations in cancer is crucial for developing targeted therapies.

Purpose of the Study:

  • To investigate the functional consequences of mutations within the histone fold in cancer genomes.
  • To identify novel mechanisms by which histone mutations contribute to tumorigenesis.
  • To provide insights into the role of epigenetic alterations in cancer development.

Main Methods:

  • Analysis of cancer genome sequencing data.
  • Functional assays to assess nucleosome stability.
  • Computational modeling of histone-DNA interactions.

Main Results:

  • Recent cancer genome analyses reveal mutations within the histone fold.
  • These mutations were found to alter nucleosome stability.
  • This provides a new mechanistic link between histone mutations and cancer.

Conclusions:

  • Mutations in the histone fold represent a novel mechanism of oncogenesis.
  • Altered nucleosome stability due to histone mutations can drive tumor formation.
  • Further research into oncohistone mutations may reveal new therapeutic targets.