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Related Concept Videos

Desmosomes01:05

Desmosomes

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The term desmosome derives from the Greek words "desmo" and "soma" meaning "adhesion bodies." This structure was first observed during the late 1800s and described as small, dense nodules in the epidermis. Desmosomes are button-like structures that help form an interlinked network of intermediate filaments across the cells. These junctions are  essential to hold cells together under mechanical stress and to maintain tissue integrity. Desmosomes are multi-protein...
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Skin cancer is a type of cancer that occurs when there is an abnormal growth of skin cells, usually triggered by damage to the DNA within the skin cells. It is primarily caused by exposure to ultraviolet (UV) radiation from the sun or artificial sources like tanning beds. Skin cancer is the most common type of cancer worldwide, and its incidence continues to rise.
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Cellular Adaptation IV: Dysplasia and Metaplasia01:24

Cellular Adaptation IV: Dysplasia and Metaplasia

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DysplasiaDysplasia refers to abnormal changes in the size, shape, and organization of mature cells, characterized by pleomorphism, nuclear abnormalities, and increased mitotic activity. It commonly affects epithelial tissues, including the cervix, gastrointestinal tract, respiratory mucosa, and endometrium. Although it may occur alongside hyperplasia, dysplasia is not a true adaptive response but a preneoplastic change with potential to progress to cancer.When confined above the basement...
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The cadherins were one of the first cell adhesion molecules discovered; the term “cadherins”   is based on their calcium-dependent adhering properties. The first cadherins discovered on the epithelial, neuronal, and placental cells were named E-cadherin, P-cadherin, and N-cadherin, respectively. These classical cadherins share sequence and structural similarities. Other cadherins, including those involved in cell signaling, are grouped into non-classical cadherins. This...
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Satellite stem cells or myosatellite cells are quiescent stem cells that Alexander Mauro first identified in 1961. These cells are located between the sarcolemma, the plasma membrane of muscle fibers, and the basal lamina, the connective tissue sheath covering it. These mononucleated cells are activated in response to muscle injury, can transform into myoblasts, and may form or repair muscle fibers. Myosatellite cells can provide additional myonuclei for muscle regeneration or return to a...
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Anchoring junctions are multiprotein complexes that help cells connect to other cells and the extracellular matrix. Anchoring junctions are present on the lateral and basal surfaces of cells, providing strong and flexible connections. Focal adhesions are often formed due to cell interactions with the ECM substrata, which initiate signal transduction via kinase cascades and other mechanisms. Together, they provide stability and tissue integrity. There are three types of anchoring junctions:...
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Related Experiment Video

Updated: Apr 23, 2026

Author Spotlight: Anterior HR-OCT as a Non-Invasive Tool for Characterizing Ocular Surface Squamous Neoplasia
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Desmosomal defects in acantholytic squamous cell carcinomas.

Charlene O'Shea1, James E Fitzpatrick, Peter J Koch

  • 1Department of Dermatology, University of Colorado School of Medicine, Aurora, CO, USA; Charles C. Gates Center for Regenerative Medicine and Stem Cell Biology, University of Colorado School of Medicine, Aurora, CO, USA.

Journal of Cutaneous Pathology
|September 30, 2014
PubMed
Summary
This summary is machine-generated.

Acantholytic squamous cell carcinoma (SCC) involves a loss of cell adhesion. This study found that desmosomal protein loss is the likely cause of this adhesion defect in acantholytic SCC.

Keywords:
Acantholytic squamous cell carcinomasDesmocollinDesmogleinDesmoplakinDesmosomes

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Area of Science:

  • Dermatology
  • Oncology
  • Cell Biology

Background:

  • Epithelial tumors known as acantholytic squamous cell carcinoma (SCC) exhibit a loss of cell adhesion between neoplastic keratinocytes.
  • The precise mechanism driving this loss of cell-cell adhesion in acantholytic SCC remains unclear.

Purpose of the Study:

  • To investigate the molecular mechanisms underlying the loss of cell-cell adhesion in acantholytic SCC.
  • To determine the role of desmosomal and adherens junction proteins in acantholytic SCC pathogenesis.

Main Methods:

  • Retrospective analysis of 17 acantholytic SCC cases and 16 conventional SCC controls.
  • Utilized immunofluorescence microscopy with antibodies targeting desmosomal and adherens junction proteins.
  • Assessed the expression patterns of cell adhesion proteins in tumor samples.

Main Results:

  • A significant majority (89%) of acantholytic SCC cases displayed focal loss of at least one desmosomal cell adhesion protein.
  • A substantial proportion (65%) of these tumors showed a loss of expression for two or more desmosomal proteins.
  • Conventional SCC cases did not exhibit similar widespread loss of desmosomal protein expression.

Conclusions:

  • The loss of cell adhesion in acantholytic SCC is strongly associated with the focal downregulation of desmosomal proteins.
  • This finding offers potential mechanistic insights into the pathogenesis of acantholytic SCC.
  • Targeting desmosomal protein pathways may represent a therapeutic strategy for acantholytic SCC.