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Related Concept Videos

Positive Regulator Molecules02:39

Positive Regulator Molecules

Mitotic cell division results in daughter cells that exactly resemble the parent cell. However, errors in the DNA replication or distribution of genetic material may lead to genetic mutations that may be passed down to every new cell formed from the resulting abnormal cell. Propagation of such mutant cells is restricted through checkpoint mechanisms present at different stages of the cell cycle. These checkpoints involve regulator molecules that either promote or demote cell cycle events.
Peroxisomes01:24

Peroxisomes

Peroxisomes are specialized organelles present in fungi, plant, and animal cells. It can vary in number, size, morphology, and activity depending on the type of tissue and the nutritional state of the cell. For example, cells with active lipid metabolism, such as adipocytes, neurons, and hepatocytes, have more peroxisomes than other cells in the body. Besides their primary role in breaking down complex organic molecules, peroxisomes can also synthesize specific macromolecules and participate in...
Meiosis II02:02

Meiosis II

Meiosis II entails cell division and segregation of the sister chromatids, resulting in the production of four unique haploid gametes. The steps for meiosis II are similar to mitosis, except that meiosis II occurs in haploid cells, whereas mitosis occurs in diploid cells.
The timing and cell division patterns of meiosis differ between males and females. In male meiosis, the centrosomes are part of the formation of the meiotic spindle. However, in oocytes, including that of humans, Drosophila,...
Cycloaddition Reactions: MO Requirements for Thermal Activation01:16

Cycloaddition Reactions: MO Requirements for Thermal Activation

Thermal cycloadditions are reactions where the source of activation energy needed to initiate the reaction is provided in the form of heat. A typical example of a thermally-allowed cycloaddition is the Diels–Alder reaction, which is a [4 + 2] cycloaddition. In contrast, a [2 + 2] cycloaddition is thermally forbidden.

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Related Experiment Video

Updated: Jul 14, 2026

Anterior High-Resolution Optical Coherence Tomography in the Diagnosis and Therapeutic Monitoring of Ocular Surface Squamous Neoplasia
06:15

Anterior High-Resolution Optical Coherence Tomography in the Diagnosis and Therapeutic Monitoring of Ocular Surface Squamous Neoplasia

Published on: August 9, 2024

Cyclooxygenase 2 expression in pterygium.

Chun-Chi Chiang1, Ya-Wen Cheng, Chien-Lin Lin

  • 1Department of Ophthalmology, China Medical University Hospital, Taichung, Taiwan. elsa10019@yahoo.com.tw <elsa10019@yahoo.com.tw>

Molecular Vision
|May 23, 2007
PubMed
Summary

Cyclooxygenase 2 (COX 2) was found in pterygium tissue, suggesting it may play a role in pterygium formation. This finding could lead to new COX 2 inhibitor treatments for pterygium.

Related Experiment Videos

Last Updated: Jul 14, 2026

Anterior High-Resolution Optical Coherence Tomography in the Diagnosis and Therapeutic Monitoring of Ocular Surface Squamous Neoplasia
06:15

Anterior High-Resolution Optical Coherence Tomography in the Diagnosis and Therapeutic Monitoring of Ocular Surface Squamous Neoplasia

Published on: August 9, 2024

Area of Science:

  • Ophthalmology
  • Oncology
  • Molecular Biology

Background:

  • Pterygium, a conjunctival overgrowth, is increasingly viewed as a neoplastic condition due to abnormal p53 gene expression.
  • Ultraviolet (UV) radiation is a known risk factor for pterygium, but the underlying cellular mechanisms remain unclear.
  • Cyclooxygenase 2 (COX 2) is implicated in UV-induced skin cancer, prompting investigation into its role in pterygium.

Purpose of the Study:

  • To investigate the expression of cyclooxygenase 2 (COX 2) in pterygium tissues.
  • To determine if COX 2 is present in pterygium and its cellular localization.

Main Methods:

  • Immunohistochemical staining was employed to detect COX 2 expression.
  • The study analyzed 90 pterygium specimens, alongside 40 normal conjunctiva and 5 normal limbus samples.

Main Results:

  • COX 2 expression was detected in 83.3% of pterygium specimens.
  • Staining was primarily localized to the cytoplasm of the epithelial layer, particularly the basal layer.
  • No significant COX 2 staining was observed in normal conjunctiva or limbus tissues.

Conclusions:

  • The presence of COX 2 in pterygium suggests its potential involvement in pterygium development.
  • These findings support the hypothesis that pterygium shares carcinogenic pathways with UV-induced cutaneous tumors.
  • Further research into the causal link between COX 2 and pterygium, and the efficacy of COX 2 inhibitors, is warranted.