[Effects of BET Bromodomain Inhibitor JQ1 on Double-Expressor Lymphoma Cell Lines and Its Mechanism]

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2022 Aug;30(4):1094-1100. doi: 10.19746/j.cnki.issn.1009-2137.2022.04.018.
[Article in Chinese]

Abstract

Objective: To investigate the effects and mechanism of bromodomain and extra-terminal (BET) inhibitor JQ1 on the double-expressor lymphoma (DEL) cell lines.

Methods: Protein expressions of cMyc and BCL-2 in 3 lymphoma cell lines were checked by Western blot so as to identify DEL cell lines. CCK-8 assay was used to detect the effects of JQ1 on anti-proliferation in the DEL cell lines. Western blot and RT-PCR were used to measure the protein and mRNA expressions of cMyc, BCL-2 and BCL-6 in DEL cell lines which treated by JQ1. Flow cytometry was used to detect the effect of JQ1 on cell apoptosis.

Results: Based on the expressions of cMyc and BCL-2, the SU-DHL6 and OCILY3 cell lines were confirmed as DEL cell lines. CCK-8 assay showed that the proliferation of DEL cell lines was inhibited by JQ1, which was similar to non-DEL cell lines and mainly regulated the expression of cMyc and BCL-6 but not BCL-2. JQ1 had no effects on apoptosis in the DEL cell lines.

Conclusion: BET inhibitor JQ1 has anti-tumor effect in the DEL cell lines, thus providing evidence for the therapeutic potential of BET inhibitor JQ1.

题目: BET抑制剂JQ1对双表达淋巴瘤细胞株的作用及其机制研究.

目的: 探讨BET抑制剂JQ1对于双表达B细胞淋巴瘤细胞株的作用机制。.

方法: Western blot检测B细胞淋巴瘤细胞株SU-DHL6、OCILY3、OCILY10 的cMyc和BCL-2蛋白的表达情况,识别双表达淋巴瘤细胞株。CCK-8方法检测JQ1对淋巴瘤细胞株增殖的影响,Western blot及RT-RCR方法检测JQ1对cMyc、BCL-2、BCL-6 mRNA及蛋白水平的影响,流式细胞术检测JQ1对淋巴瘤细胞株凋亡的影响。.

结果: SU-DHL6、OCILY3同时表达cMyc和BCL-2,为双表达淋巴瘤细胞株。CCK-8结果显示,JQ1对双表达淋巴瘤细胞株的增殖有抑制作用,并且JQ1主要调节cMyc、BCL-6的表达,对BCL-2无明显影响,且对B淋巴瘤细胞株凋亡无影响。.

结论: BET抑制剂JQ1可调节cMyc、BCL-6表达,抑制B细胞淋巴瘤增殖。.

Keywords: JQ1; Myc; double-expressor lymphoma.

MeSH terms

  • Apoptosis
  • Azepines* / pharmacology
  • Cell Line, Tumor
  • Cell Proliferation
  • Humans
  • Proto-Oncogene Proteins c-myc* / metabolism
  • Triazoles / pharmacology
  • Xenograft Model Antitumor Assays

Substances

  • Azepines
  • Proto-Oncogene Proteins c-myc
  • Triazoles