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反义c-myc和免疫刺激寡核苷酸对小鼠B细胞淋巴瘤移植模型中肿瘤发生的抑制作用

Antisense c-myc and immunostimulatory oligonucleotide inhibition of tumorigenesis in a murine B-cell lymphoma transplant model.

作者信息

Smith J B, Wickstrom E

机构信息

Department of Microbiology and Immunology, Kimmel Cancer Center, and Cardeza Foundation for Hematological Research, Thomas Jefferson University, Philadelphia, PA 19107, USA.

出版信息

J Natl Cancer Inst. 1998 Aug 5;90(15):1146-54. doi: 10.1093/jnci/90.15.1146.

Abstract

BACKGROUND

Because the development of drug-resistant cells can lead to relapses in patients with lymphoma treated with chemotherapy, new approaches are needed for effective disease management, such as those targeting the c-MYC proto-oncogene with antisense oligonucleotides. Our goal was to investigate whether antisense c-myc oligonucleotides could prevent tumorigenesis in a B-cell lymphoma model.

METHODS

Immunocompetent mice received subcutaneous injections of tumor cells from a transgenic mouse model of Burkitt's lymphoma. For 7 consecutive days, beginning 1 day after tumor cell transplantation, the mice were given either a DNA phosphorothioate oligonucleotide complementary to c-myc codons 1-5 (myc6) or other c-myc-related oligonucleotides at a dose of 0.76 mg per day subcutaneously. Myc protein expression, normalized to beta-actin expression, was measured by western blotting of tumor and splenic proteins. To determine whether tumor inhibition by myc6 could be a result of B-cell activation, we compared the activity of myc6 with that of an immunostimulatory oligonucleotide, mcg.

RESULTS

In comparison with control treatments (saline vehicle, scrambled-sequence oligonucleotide, or double-mismatch oligonucleotide), treatment with myc6 delayed tumor onset by 3 days, decreased total tumor mass at sacrifice (i.e., 17 days after tumor cell transplantation) by 40% +/- 16% (mean +/- standard error), and decreased the splenic Myc-to-actin ratio. Inhibition of tumors by myc6 and mcg (both of which share a dACGTT motif) was comparable. Administration of an oligonucleotide sequence complementary to c-myc codons 384-388 (myc55) delayed tumor onset by 5-6 days, decreased total tumor mass at sacrifice by 65% +/- 6%, and reduced the splenic Myc-to-actin ratio to below that produced by myc6. A 14-day treatment regimen of myc55 alternating with mcg completely inhibited tumor formation during the therapeutic schedule.

CONCLUSIONS

A combined oligonucleotide regimen, based on antisense c-MYC and immunostimulatory oligonucleotides, should be investigated to increase the number and duration of complete remissions obtained after standard chemotherapy for B-cell lymphoma.

摘要

背景

由于耐药细胞的产生会导致接受化疗的淋巴瘤患者复发,因此需要新的方法来有效管理疾病,例如用反义寡核苷酸靶向c-MYC原癌基因。我们的目标是研究反义c-myc寡核苷酸是否能在B细胞淋巴瘤模型中预防肿瘤发生。

方法

免疫活性小鼠皮下注射来自伯基特淋巴瘤转基因小鼠模型的肿瘤细胞。从肿瘤细胞移植后1天开始,连续7天,每天皮下给予小鼠与c-myc密码子1-5互补的DNA硫代磷酸寡核苷酸(myc6)或其他与c-myc相关的寡核苷酸,剂量为0.76毫克。通过对肿瘤和脾脏蛋白进行蛋白质印迹法,以β-肌动蛋白表达为标准,测量Myc蛋白表达。为了确定myc6对肿瘤的抑制作用是否可能是B细胞激活的结果,我们将myc6的活性与免疫刺激寡核苷酸mcg的活性进行了比较。

结果

与对照处理(生理盐水载体、乱序寡核苷酸或双错配寡核苷酸)相比,用myc6处理使肿瘤发生延迟3天,处死时(即肿瘤细胞移植后17天)的总肿瘤质量降低40%±16%(平均值±标准误差),并降低了脾脏中Myc与肌动蛋白的比例。myc6和mcg(两者都有dACGTT基序)对肿瘤的抑制作用相当。给予与c-myc密码子384-388互补的寡核苷酸序列(myc55)使肿瘤发生延迟5-6天,处死时的总肿瘤质量降低65%±6%,并使脾脏中Myc与肌动蛋白的比例降至低于myc6所产生的水平。myc55与mcg交替使用的14天治疗方案在治疗期间完全抑制了肿瘤形成。

结论

应研究基于反义c-MYC和免疫刺激寡核苷酸的联合寡核苷酸方案,以增加B细胞淋巴瘤标准化疗后完全缓解的次数和持续时间。

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