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Related Concept Videos

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,...
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,...
Rous Sarcoma Virus (RSV) and Cancer01:03

Rous Sarcoma Virus (RSV) and Cancer

Rous Sarcoma virus or RSV was discovered by F. Peyton Rous in the year 1911 as a filterable transmissible agent that could cause tumors in chickens. He won a Nobel Prize for this discovery in 1966. His experiments clearly demonstrated that some cancers could be caused by infectious agents and led to the discovery of many more cancer-causing viruses in animals as well as humans.
RSV is a retrovirus that contains two copies of a plus-strand  RNA genome. Its genome consists of four main open...
Rous Sarcoma Virus (RSV) and Cancer01:03

Rous Sarcoma Virus (RSV) and Cancer

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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.
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The Ras Gene

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Spatial and Temporal Control of Murine Melanoma Initiation from Mutant Melanocyte Stem Cells
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Published on: June 7, 2019

BRCA1 gene mutation in thymic malignant melanoma.

Eun Jue Yi1, Jong Ho Park, Hae Won Lee

  • 1Department of Thoracic Surgery, Korea Cancer Center Hospital, Korea Institute of Radiological and Medical Sciences, Seoul, Republic of Korea.

The Annals of Thoracic Surgery
|August 6, 2013
PubMed
Summary

A patient developed three distinct cancers: thyroid, ovarian, and thymic malignant melanoma. Genetic testing identified a BRCA1 gene mutation, suggesting a link between this mutation and multiple primary cancers.

Keywords:
13

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Area of Science:

  • Oncology
  • Genetics
  • Cancer Biology

Background:

  • Multiple primary malignancies present a complex clinical challenge.
  • Understanding the genetic underpinnings of synchronous or metachronous cancers is crucial for personalized medicine.

Observation:

  • A case study of a patient diagnosed with three independent primary cancers: thyroid cancer, ovarian cancer, and thymic malignant melanoma.
  • The occurrence of these three distinct malignancies in a single patient prompted investigation into potential shared genetic factors.

Findings:

  • Blood analysis revealed the presence of germline BRCA1 gene mutations in the patient.
  • This finding suggests a potential genetic predisposition contributing to the development of these specific triple primary malignancies.

Implications:

  • The identification of BRCA1 mutations in this context may inform genetic counseling and screening protocols for patients with multiple primary cancers.
  • Further research into the role of BRCA1 and other genetic mutations in the etiology of rare cancer combinations is warranted.