Retinoblastoma Cells

Retinoblastoma is a rare type of eye cancer that usually affects children under the age of five. It begins in the retina, the part of the eye that sends visual signals to the brain. The cancerous cells in retinoblastoma are referred to as retinoblastoma cells. These cells are highly specialized and have unique characteristics that distinguish them from normal cells. They are characterized by uncontrolled growth and division, which allows them to form a tumor in the retina. Retinoblastoma cells can also invade and spread to other parts of the body if left untreated. Researchers have been studying retinoblastoma cells extensively to better understand the disease and develop new treatments. They have discovered that mutations in the RB1 gene, which normally helps regulate cell growth and division, are often present in retinoblastoma cells. These mutations can interfere with the normal function of the gene, leading to uncontrolled cell growth and division. Various treatment options are available for retinoblastoma, including chemotherapy, radiation therapy, and surgery. In some cases, a combination of treatments may be used to achieve the best possible outcome. In summary, retinoblastoma cells are the cancerous cells that form in the retina and cause retinoblastoma. Understanding the characteristics and behavior of these cells is crucial for developing effective therapies that can improve the prognosis and quality of life for individuals with this disease.


From: Journal of Ophthalmic Science

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