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首页> 外文期刊>Leukemia >Translocation t(14;18) and gain of chromosome 18|[sol]|BCL2: effects on BCL2 expression and apoptosis in B-cell non-Hodgkin's lymphomas
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Translocation t(14;18) and gain of chromosome 18|[sol]|BCL2: effects on BCL2 expression and apoptosis in B-cell non-Hodgkin's lymphomas

机译:t(14; 18)易位和染色体18 | [sol] | BCL2的获得:对B细胞非霍奇金淋巴瘤BCL2表达和凋亡的影响

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摘要

Gain of chromosome 18q and translocation t(14;18) are] frequently found in B-cell non-Hodgkin's lymphomas (B-NHL). Increased BCL2 transcription and BCL2 protein expression have been suggested to be the result of the gain. We utilized FISH, PCR and array CGH to study BCL2 and chromosome 18 copy number changes and rearrangements in 93 cases of B-NHL. BCL2 protein was expressed in >75% of the tumor cells in 92% of the cases by immunohistochemistry. Gain of BCL2 was associated with a 25% increase in BCL2 expression levels (immunoblotting), whereas t(14;18) resulted in a 55% increase in BCL2 levels compared to cases without BCL2 alterations. The tumor cell (spontaneous) apoptotic fractions were similar for the cases with different BCL2 genotypes. However, the normal cell apoptotic fractions were higher for the tumors with t(14;18) compared to the tumors without BCL2 alterations, while the tumors with gain of BCL2 only showed intermediate levels. Low-level gains of parts of chromosome 18 were found in 14 of the 38 B-NHL cases with t(14;18), with a consensus region 18pter-q21.33 that did not include the BCL2 gene. The 11 cases with 18q gain only showed a consensus region encompassing 18q21.2–18q21.32 and 18q21.33, which contain PMAIP1/MALT1 and BCL2, respectively.
机译:]在B细胞非霍奇金淋巴瘤(B-NHL)中经常发现18q染色体的获得和易位t(14; 18)。 BCL2转录和BCL2蛋白表达增加已被认为是获得的结果。我们利用FISH,PCR和CGH阵列研究了93例B-NHL中BCL2和18号染色体拷贝数的变化和重排。通过免疫组织化学,在92%的病例中,BCL2蛋白在> 75%的肿瘤细胞中表达。与无BCL2改变的病例相比,BCL2的增加与BCL2的表达水平增加25%(免疫印迹)相关,而t(14; 18)导致BCL2的水平增加55%。对于具有不同BCL2基因型的病例,肿瘤细胞(自发的)凋亡分数相似。然而,与没有BCL2改变的肿瘤相比,具有t(14; 18)的肿瘤的正常细胞凋亡分数更高,而具有BCL2改变的肿瘤仅显示中等水平。在38例t(14; 18)的B-NHL病例中,有14例发现了18号染色体部分的低水平增益,共有区域18pter-q21.33不包括BCL2基因。 11例18q增高病例仅显示出一个共有区域,包括18q21.2-18q21.32和18q21.33,分别包含PMAIP1 / MALT1和BCL2。

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