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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...
Pigmentation01:19

Pigmentation

The color of the skin is influenced by a number of pigments, including melanin, carotene, and hemoglobin. Recall that melanin is produced by cells called melanocytes, which are found scattered throughout the stratum basale of the epidermis. The melanin is transferred to the keratinocytes via melanosomes.
Melanin occurs in two primary forms: eumelanin that provides black and brown pigment and pheomelanin that provides red color. Dark-skinned individuals produce more melanin than those with pale...
Cancer Prevention02:59

Cancer Prevention

Several factors can increase the risk of cancer in an individual. About 50% of cancer cases can be prevented by adopting a healthy lifestyle, regular exercise, eating healthy, and following a modest cancer prevention diet. Epidemiological studies have consistently shown that populations with vegetable and fruit-rich diets have reduced the incidence of cancer. On the other hand, populations who have a diet rich in animal fat, red meat, junk food, or high calories are predisposed to cancer.
Some...
Cancers Originate from Somatic Mutations in a Single Cell02:21

Cancers Originate from Somatic Mutations in a Single Cell

Cancer arises from mutations in the critical genes that allow healthy cells to escape cell cycle regulation and acquire the ability to proliferate indefinitely. Though originating from a single mutation event in one of the originator cells, cancer progresses when the mutant cell lines continue to gain more and more mutations, and finally, become malignant. For example, chronic myelogenous leukemia (CML) develops initially as a non-lethal increase in white blood cells, which progressively...
Cancers Originate from Somatic Mutations in a Single Cell02:21

Cancers Originate from Somatic Mutations in a Single Cell

Cancer arises from mutations in the critical genes that allow healthy cells to escape cell cycle regulation and acquire the ability to proliferate indefinitely. Though originating from a single mutation event in one of the originator cells, cancer progresses when the mutant cell lines continue to gain more and more mutations, and finally, become malignant. For example, chronic myelogenous leukemia (CML) develops initially as a non-lethal increase in white blood cells, which progressively...
The Retinoblastoma Gene01:20

The Retinoblastoma Gene

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.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...

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Related Experiment Video

Updated: Jun 27, 2026

Pharmacologic Induction of Epidermal Melanin and Protection Against Sunburn in a Humanized Mouse Model
12:37

Pharmacologic Induction of Epidermal Melanin and Protection Against Sunburn in a Humanized Mouse Model

Published on: September 7, 2013

Melanoma and genetics.

Andrew A Nelson1, Hensin Tsao

  • 1Department of Dermatology, Harvard Medical School, Boston, MA 02114, USA.

Clinics in Dermatology
|December 20, 2008
PubMed
Summary
This summary is machine-generated.

Genetic factors significantly influence melanoma risk. Key genes like CDKN2A, CDK4/6, RB1, and MC1R are implicated, though many genetic variants remain undiscovered. DNA analysis may predict melanoma risk in the future.

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Spatial and Temporal Control of Murine Melanoma Initiation from Mutant Melanocyte Stem Cells
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A Robust Discovery Platform for the Identification of Novel Mediators of Melanoma Metastasis
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A Robust Discovery Platform for the Identification of Novel Mediators of Melanoma Metastasis

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Last Updated: Jun 27, 2026

Pharmacologic Induction of Epidermal Melanin and Protection Against Sunburn in a Humanized Mouse Model
12:37

Pharmacologic Induction of Epidermal Melanin and Protection Against Sunburn in a Humanized Mouse Model

Published on: September 7, 2013

Spatial and Temporal Control of Murine Melanoma Initiation from Mutant Melanocyte Stem Cells
06:09

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A Robust Discovery Platform for the Identification of Novel Mediators of Melanoma Metastasis
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A Robust Discovery Platform for the Identification of Novel Mediators of Melanoma Metastasis

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Area of Science:

  • Genetics
  • Dermatology
  • Oncology

Background:

  • Malignant melanoma incidence is rising globally.
  • Genetic predisposition plays a role in some melanoma cases, while sporadic cases may involve moderate-risk genetic factors.
  • Human genome sequencing advances drive research into melanoma-associated genes.

Purpose of the Study:

  • To review genes conferring the greatest risk for developing melanoma.
  • To highlight the importance of both high-risk and moderate-risk genetic factors.
  • To discuss the current understanding and future directions in melanoma genetics.

Main Methods:

  • Literature review of genetic factors associated with melanoma.
  • Focus on well-established high-risk genes and moderate-risk genes.
  • Discussion of gene functions in cell cycle regulation and apoptosis.

Main Results:

  • Heritable alterations in cyclin-dependent kinase inhibitor 2A (CDKN2A) represent the strongest genetic risk.
  • CDKN2A encodes p16/INK4a and p14/ARF proteins, crucial for cell division and apoptosis.
  • Other significant genes include CDK4/6, retinoblastoma (RB1), and the melanocortin 1 receptor (MC1R).

Conclusions:

  • Significant advances have been made in understanding melanoma's molecular and genetic basis.
  • Many melanoma cases likely result from undiscovered genetic variants.
  • Future DNA analysis may enable personalized melanoma risk prediction, requiring integration with clinical utility.