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Latexin Is Down-Regulated in Hematopoietic Malignancies and Restoration of Expression Inhibits Lymphoma Growth

机译:Latexin下调的造血系统恶性肿瘤和表达抑制淋巴瘤恢复性增长

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摘要

Latexin is a negative regulator of hematopoietic stem cell number in mice. Its dysregulated expression in other tumors led us to hypothesize that latexin may have tumor suppressor properties in hematological malignancies. We found that latexin was down-regulated in a variety of leukemia and lymphoma cell lines as well as in CD34+ cells from the blood and marrow of patients with these malignancies. 5-aza-2′-deoxycytodine treatment and bisulfite sequencing revealed hypermethylation of latexin promoter in tumor cells. Retrovirus-mediated latexin overexpression in A20 mouse lymphoma cells inhibited their in vitro growth by 16 fold and in vivo tumor volume by 2 fold. Latexin caused growth inhibition of lymphoma cells by significantly increasing apoptosis through the down-regulation of anti-apoptotic genes Bcl-2 and Pim-2. The molecular mechanism underlying latexin-mediated tumor inhibition was not through its canonical carboxypeptidase inhibitor activity. These results are consistent with a tumor suppressor role for latexin and suggest that latexin may have clinical efficacy in the treatment of malignancies.
机译:Latexin是小鼠造血干细胞数量的负调节剂。它在其他肿瘤中的表达失调使我们假设乳胶在血液恶性肿瘤中可能具有抑癌作用。我们发现,在患有这些恶性肿瘤的患者的血液和骨髓中,各种白血病和淋巴瘤细胞系以及CD34 +细胞中的乳胶蛋白均被下调。 5-氮杂-2'-脱氧胞嘧啶的处理和亚硫酸氢盐测序揭示了肿瘤细胞中乳胶启动子的高度甲基化。逆转录病毒介导的A20小鼠淋巴瘤细胞中的乳胶过表达将其体外生长抑制16倍,将体内肿瘤体积抑制2倍。 Latexin通过下调抗凋亡基因Bcl-2和Pim-2来显着增加细胞凋亡,从而导致淋巴瘤细胞的生长受到抑制。乳胶介导的肿瘤抑制的分子机制不是通过其典型的羧肽酶抑制剂活性。这些结果与乳胶的肿瘤抑制作用相一致,表明乳胶可能具有治疗恶性肿瘤的临床功效。

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