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Frequent Mutation of BAP1 in Metastasizing Uveal Melanomas
Author(s) -
J. William Harbour,
Michael D. Onken,
Elisha Roberson,
Shenghui Duan,
Li Cao,
Lori A. Worley,
M. Laurin Council,
Katie A. Matatall,
Cynthia Helms,
A. Bowcock
Publication year - 2010
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.1194472
Subject(s) - bap1 , melanoma , mutation , cancer research , medicine , biology , genetics , gene
An Eye on Metastasis Despite the considerable progress being made in elucidating the cell biology of metastasis, little is known about the genetic alterations that promote metastasis of human tumors, the cause of most cancer deaths. A potentially important clue now emerges from the work ofHarbouret al. (p.1410 , published online 4 November), who used an exome-sequencing approach to search for genetic mutations in uveal melanomas, an eye cancer associated with a high rate of fatal metastasis. Remarkably, over 80% of tumor samples with a high metastatic risk had inactivating somatic mutations in the gene encoding BAP1 (BRCA1-associated protein 1), a nuclear protein involved in controlling protein degradation. Thus, in this tumor type, mutational inactivation of BAP1 may be a key event in the acquisition of metastatic competence.

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