Chromosome 9 Short Arm Deletions in Malignant Diseases

Abstract

Deletions of 9p21-22, that frequently include the α-, β-and ω-IFN gene cluster, are common in malignant diseases such as acute lymphocytic leukemia, malignant melanoma and malignant glioma. There is also evidence to support the role of a gene(s) on chromosome 9p21 in predisposition for familial malignant melanoma.

Although initial studies implicated that the IFN genes could serve as tumor suppressor genes, there is now data, mainly based on estimations of minimum region of overlap for the deletions, indicating that the relevant tumor suppressor gene is located centromeric of the α-, β-, ω-IFN gene cluster.

Key Words:

• Chromosome 9
• interferon
• tumor suppressor genes