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建立一个新型的人淋巴母细胞株,其 11 号染色体长臂异常,但没有 MLL 重排。

Establishment of a novel human lymphoblastic cell strain with the long arm of chromosome 11 aberration without MLL rearrangement.

机构信息

Department of Hematology, HuaShan Hospital Affiliated of FuDan University, No. 12 Middle WuLumuqi Road, Shanghai, 200040, P.R. China.

Department of Pathology, ChangHai Hospital Affiliated of Second Military Medical University, No. 168 Changhai Road, Shanghai, 200433, P.R. China.

出版信息

Sci Rep. 2017 Apr 13;7(1):867. doi: 10.1038/s41598-017-00874-6.

DOI:10.1038/s41598-017-00874-6
PMID:28408741
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5429836/
Abstract

At present, all cell strains derived from acute lymphoblastic leukemia (ALL) patients with the long arm of chromosome 11 aberration are accompanied with mixed lineage leukemia (MLL) gene rearrangement. In this study, we established a permanent ALL cell strain CHH-1 with the long arm of chromosome 11 aberration and without MLL rearrangement, hoping that it could be used for the research of ALL with such genetic abnormality. CHH-1 cell strain was certified through morphology, immunophenotype, genetics and immunoglobulin (Ig) gene rearrangement analysis. Cell characteristics including tumorigenic ability, semisolid colony forming ability, telomerase activity, autocrine and invasion were further detected. Cells were with an add(11)(q23) structural abnormality without MLL rearrangement, and were consistent with the genetic abnormality of the patient. In addition, these cells had features of tumor-forming ability, high colony forming capacity, unique cytokine autocrine mode, high telomerase activity, and high invasion ability. CHH-1 may prove to be a useful cell model for the research of human leukemia with genetic aberration in chromosome 11, and help explore the role of such genetic abnormality in the pathogenesis, progression and prognosis of ALL, and in developing new target drugs.

摘要

目前,所有源于伴有 11 号染色体长臂异常的急性淋巴细胞白血病(ALL)患者的细胞株均伴有混合谱系白血病(MLL)基因重排。本研究建立了一株不伴有 MLL 重排的伴有 11 号染色体长臂异常的永生化 ALL 细胞株 CHH-1,希望能用于此类遗传学异常的 ALL 的研究。通过形态学、免疫表型、遗传学和免疫球蛋白(Ig)基因重排分析对 CHH-1 细胞株进行了鉴定。进一步检测了细胞的特征,包括致瘤能力、半固体集落形成能力、端粒酶活性、自分泌和侵袭能力。细胞具有 11q23 结构异常而无 MLL 重排,与患者的遗传学异常一致。此外,这些细胞具有成瘤能力、高集落形成能力、独特的细胞因子自分泌模式、高端粒酶活性和高侵袭能力。CHH-1 可能被证明是研究具有染色体 11 号遗传学异常的人类白血病的有用细胞模型,有助于探索这种遗传异常在 ALL 的发病机制、进展和预后中的作用,并有助于开发新的靶向药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996a/5429836/c1352afec672/41598_2017_874_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996a/5429836/bf1b9777be4f/41598_2017_874_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996a/5429836/da343fbc6658/41598_2017_874_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996a/5429836/aeb9792c3161/41598_2017_874_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996a/5429836/4bd8cdaf4b3f/41598_2017_874_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996a/5429836/2ad58197cae9/41598_2017_874_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996a/5429836/c1352afec672/41598_2017_874_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996a/5429836/bf1b9777be4f/41598_2017_874_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996a/5429836/da343fbc6658/41598_2017_874_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996a/5429836/aeb9792c3161/41598_2017_874_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996a/5429836/4bd8cdaf4b3f/41598_2017_874_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996a/5429836/2ad58197cae9/41598_2017_874_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996a/5429836/c1352afec672/41598_2017_874_Fig6_HTML.jpg

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