Mutation in SF3B1 gene promotes formation of polyploid giant cells in Leukemia cells

被引:10
作者
Mukherjee, Sanjay [1 ]
Ali, Abdullah Mahmood [1 ]
Murty, Vundavalli V. [2 ,3 ]
Raza, Azra [1 ,4 ,5 ]
机构
[1] Columbia Univ, Dept Med, Div Hematol Oncol, Irving Med Ctr, New York, NY 10032 USA
[2] Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY 10032 USA
[3] Columbia Univ, Inst Canc Genet, Dept Med, Irving Med Ctr, New York, NY 10032 USA
[4] Columbia Univ, Herbert Irving Comprehens Canc Ctr, New York, NY 10032 USA
[5] Columbia Univ, MDS Ctr, Irving Med Ctr, 177 Ft Washington Ave,Milstein Hosp Bldg, New York, NY 10032 USA
基金
美国国家卫生研究院;
关键词
Polyploid giant cells; Leukemia; Cancer; ACUTE MYELOID-LEUKEMIA; ERYTHROID-DIFFERENTIATION; MYELODYSPLASTIC SYNDROME; MITOTIC CATASTROPHE; TUMOR-CELLS; CANCER; EXPRESSION; KEY; TETRAPLOIDY; LINE;
D O I
10.1007/s12032-022-01652-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Giant cells with polyploidy, termed polyploid giant cells, have been observed during normal growth, development, and pathologic states, such as solid cancer progression and resistance to therapy. Functional studies of polyploidal giant cancer cells (PGCC) provided evidence that they arise when normal diploid cells are stressed, show stem cell-like properties, and give rise to tumors. In the present study, we report in K562 leukemia cell line that introduction of the hotspot K700E mutation in the gene SF3B1 using CRISPR/Cas9 method results in an increased frequency of multinucleated polyploid giant cells resistant to chemotherapeutic agent and serum starvation stress. These giant cells with higher ploidy are distinct from multinucleated megakaryocytes, are proliferative, and are characterized by increased accumulation of mitochondria. PGCC have been previously documented in solid tumors. This is the first report describing PGCCs in a cell line derived from a liquid cancer where increased frequency of PGCCs is linked to a specific genetic event. Since SF3B1 mutations are predominantly seen in MDS and other hematologic malignancies, our current findings will have significant clinical implications.
引用
收藏
页数:14
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