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Related Concept Videos

Skin Cancer01:30

Skin Cancer

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.
Basal Cell Carcinoma (BCC): BCC is the most common type of skin cancer, accounting for about 80% of cases. It typically develops in...
Cellular Adaptation III: Hyperplasia01:26

Cellular Adaptation III: Hyperplasia

Hyperplasia is an increase in the number of cells in a tissue or organ due to enhanced cell division. It is an adaptive, controlled response to stimuli such as injury, hormones, or stress, involving mitosis to produce genetically identical cells and support tissue repair and regeneration.Tissue CapacityCertain tissues, including the epidermis, intestinal epithelium, bone marrow, and fibroblasts, have a high potential for hyperplasia. Others, such as bone, cartilage, and smooth muscle, show...
Cellular Adaptation IV: Dysplasia and Metaplasia01:24

Cellular Adaptation IV: Dysplasia and Metaplasia

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...
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against specific...
Combination Therapies and Personalized Medicine02:50

Combination Therapies and Personalized Medicine

Combining two or more treatment methods increases the life span of cancer patients while reducing damage to vital organs or tissue from the overuse of a single treatment. Combination therapy also targets different cancer-inducing pathways, thus reducing the chances of developing resistance to treatment.
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
Cancer Stem Cells and Tumor Maintenance02:40

Cancer Stem Cells and Tumor Maintenance

Early diagnosis and treatment can often cure cancer. However, even with treatment, residual cells called cancer stem cells (CSC) might remain, often causing tumor recurrence. These cancer stem cells possess the potential for self-renewal and multi-lineage differentiation and are often responsible for the therapeutic resistance displayed in most cancers.
Cancer stem cells are thought to originate from tissue-specific normal stem cells or progenitor cells. The normal stem cells usually reside in...

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Related Experiment Video

Updated: May 29, 2026

Cell Population Analyses During Skin Carcinogenesis
06:53

Cell Population Analyses During Skin Carcinogenesis

Published on: August 21, 2013

Concurrent basal cell and squamous cell carcinomas associated with hydroxyurea therapy.

Jelena Radić1, Tanja Batinac, Ita Hadžisejdić

  • 1Department of Pathology, School of Medicine, University of Rijeka, Croatia.

Acta Dermatovenerologica Croatica : ADC
|September 22, 2011
PubMed
Summary

Hydroxyurea (HU) therapy may increase skin cancer risk. This case study suggests a link between HU, DNA repair, and concurrent basal cell and squamous cell carcinomas, even without HPV.

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

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Last Updated: May 29, 2026

Cell Population Analyses During Skin Carcinogenesis
06:53

Cell Population Analyses During Skin Carcinogenesis

Published on: August 21, 2013

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:

  • Dermatology
  • Oncology
  • Pharmacology

Background:

  • Long-term hydroxyurea (HU) therapy is used for myeloproliferative neoplasms like polycythemia vera.
  • Cutaneous malignancies are a known side effect, but concurrent dual primary skin cancers are rare.
  • Ultraviolet (UV) exposure is a primary risk factor for skin cancer.

Observation:

  • A 76-year-old woman on long-term HU developed two distinct primary skin cancers on the same hand: basal cell carcinoma and sarcomatoid squamous cell carcinoma.
  • Histopathology confirmed distinct tumor types with specific protein expressions (bcl-2, vimentin, EMA, CK5/6, p53).
  • Low-risk human papillomavirus (HPV) was detected in surrounding skin but not within the tumors.

Findings:

  • The concurrence of two different skin carcinomas, in the absence of HPV, suggests a potential role for mutagenic HU therapy.
  • HU may influence DNA synthesis and repair mechanisms, exacerbating UV-induced carcinogenesis.
  • p53 overexpression was noted in both tumor types, indicating potential DNA damage response alterations.

Implications:

  • Patients on HU therapy with cutaneous side effects warrant close dermatological monitoring.
  • Hydroxyurea's potential mutagenicity necessitates a re-evaluation of risk factors in skin cancer development.
  • Consideration of HU's role in skin carcinogenesis is crucial, especially in sun-exposed individuals.