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Estimation of the timing of BAP1 mutation in uveal melanoma progression
被引:33
|作者:
Uner, Ogul E.
[1
,2
,3
]
See, Thonnie Rose O.
[2
,3
]
Szalai, Eszter
[4
]
Grossniklaus, Hans E.
[2
,3
]
Stalhammar, Gustav
[5
,6
]
机构:
[1] Emory Univ, Sch Med, Atlanta, GA USA
[2] Emory Univ, Sch Med, Dept Ophthalmol, Atlanta, GA 30322 USA
[3] Emory Univ, Sch Med, Dept Pathol, Atlanta, GA 30322 USA
[4] Univ Pecs, Sch Med, Dept Ophthalmol, Pecs, Hungary
[5] St Erik Eye Hosp, Stockholm, Sweden
[6] Karolinska Inst, Dept Clin Neurosci, Stockholm, Sweden
基金:
美国国家卫生研究院;
关键词:
GENE-EXPRESSION CLASS;
DOUBLING TIMES;
METASTASIS;
HETEROGENEITY;
PROGNOSIS;
SURVIVAL;
D O I:
10.1038/s41598-021-88390-6
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Uveal melanoma is the most common primary intraocular malignancy. A vast majority of metastasizing tumors have mutations in the BAP1 gene. Here, we investigate the spatiotemporal timing of these mutations. The size of 177 uveal melanomas and 8.3 million individual tumor cells was measured. BAP1 sequencing results and BAP1 IHC were available and for 76 (43%) and 101 (57%) of these, respectively. Tumors with a BAP1 mutation had significantly larger volume (2109 vs. 1552 mm(3), p=0.025). Similarly, tumor cells with loss of BAP1 protein expression had significantly larger volume (2657 vs. 1593 mu m(3), p=0.027). Using observations of the time elapsed between mitoses, the BAP1 mutation was calculated to occur when the primary tumor had a size of a few malignant cells to 6 mm(3), 0.5 to 4.6 years after tumor initiation and at least 9 years before diagnosis. We conclude that BAP1 mutations occur early in the growth of uveal melanoma, well before the average tumor is diagnosed. Its timing coincides with the seeding of micrometastases.
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页数:10
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