Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Exp Hematol. 2020 Apr;84:45-53.e1. doi: 10.1016/j.exphem.2020.02.004. Epub 2020 Mar 5.
Cyclin D1 (CCND1) overexpression is an early and unifying oncogenic event in mantle cell lymphoma (MCL) and multiple myeloma (MM) with chromosome 11q13 abnormalities. Herein, we report newly discovered transcript variants of the CCND1 gene in MCL and MM cells with chromosome 11q13 abnormalities. These transcript variants, designated CCND1.tv., covered the full-length coding region of CCND1 with longer 5'-untranslated regions (5'-UTRs) of CCND1 and occasionally contained a novel exon. CCND1.tv. was specifically detectable in patient-derived primary MCL or MM cells with chromosomal translocation t(11;14)(q13;q32), but not in t(11;14)-negative cells. The lengths of the 5'-UTR sequences of CCND1.tv. differed among patients and cell lines. Introduction of CCND1.tv. led to increased expression of normal-sized CCND1 protein in HEK293 cells. Furthermore, mTOR inhibition by rapamycin or serum starvation reduced ectopic expression of CCND1.tv.-derived CCND1 protein, but not 5'-UTR less CCND1-derived CCND1 protein in HEK293 cells, suggesting that the protein expression of CCND1.tv. is regulated by the mTOR pathway. Our results suggest that the aberrant expression of CCND1.tv. may contribute to the understanding of the pathogenesis of MCL and MM with 11q13 abnormalities.
Cyclin D1 (CCND1) 过表达是套细胞淋巴瘤 (MCL) 和多发性骨髓瘤 (MM) 中染色体 11q13 异常的早期和统一的致癌事件。在此,我们报告了在具有染色体 11q13 异常的 MCL 和 MM 细胞中发现的 CCND1 基因的新转录变体。这些转录变体,命名为 CCND1.tv.,覆盖了 CCND1 的全长编码区,具有更长的 CCND1 5'-非翻译区 (5'-UTR),偶尔包含一个新的外显子。CCND1.tv. 仅在具有染色体易位 t(11;14)(q13;q32)的患者来源的原发性 MCL 或 MM 细胞中特异性检测到,但在 t(11;14)-阴性细胞中则检测不到。CCND1.tv. 的 5'-UTR 序列长度在不同患者和细胞系之间存在差异。在 HEK293 细胞中引入 CCND1.tv. 导致正常大小的 CCND1 蛋白的表达增加。此外,雷帕霉素或血清饥饿抑制 mTOR 可降低 HEK293 细胞中外源表达的 CCND1.tv.衍生的 CCND1 蛋白,但不能降低 5'-UTR 缺失的 CCND1 衍生的 CCND1 蛋白,表明 CCND1.tv. 的蛋白表达受 mTOR 途径调控。我们的结果表明,CCND1.tv. 的异常表达可能有助于理解具有 11q13 异常的 MCL 和 MM 的发病机制。