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GLIPR1 表达在多发性骨髓瘤中降低,但在小鼠中不是肿瘤抑制因子。

GLIPR1 expression is reduced in multiple myeloma but is not a tumour suppressor in mice.

机构信息

Adelaide Medical School, Faculty of Health and Medical Sciences, University of Adelaide, Adelaide, Australia.

Cancer Program, Precision Medicine Theme, South Australian Health and Medical Research Institute, Adelaide, Australia.

出版信息

PLoS One. 2020 Jan 29;15(1):e0228408. doi: 10.1371/journal.pone.0228408. eCollection 2020.

Abstract

Multiple myeloma, a plasma cell malignancy, is a genetically heterogeneous disease and the genetic factors that contribute to its development and progression remain to be fully elucidated. The tumour suppressor gene GLIPR1 has previously been shown to be deleted in approximately 10% of myeloma patients, to inhibit the development of plasma cell tumours in ageing mice and to have reduced expression levels in the plasma cells of patients with light-chain amyloidosis, a myeloma-related malignancy. Therefore, we hypothesised that GLIPR1 may have tumour suppressor activity in multiple myeloma. In this study, we demonstrate that plasma cell expression of GLIPR1 is reduced in the majority of myeloma patients and Glipr1 expression is lost in the 5TGM1 murine myeloma cell line. However, overexpression of GLIPR1 in a human myeloma cell line did not affect cell proliferation in vitro. Similarly, re-expression of Glipr1 in 5TGM1 cells did not significantly reduce their in vitro proliferation or in vivo growth in C57BL/KaLwRij mice. In addition, using CRISPR-Cas9 genome editing, we generated C57BL/Glipr1-/- mice and showed that loss of Glipr1 in vivo did not affect normal haematopoiesis or the development of monoclonal plasma cell expansions in these mice up to one year of age. Taken together, our results suggest that GLIPR1 is unlikely to be a potent tumour suppressor in multiple myeloma. However, it remains possible that the down-regulation of GLIPR1 may cooperate with other genetic lesions to promote the development of myeloma.

摘要

多发性骨髓瘤是一种浆细胞恶性肿瘤,具有遗传异质性,其发生和发展的遗传因素仍有待充分阐明。肿瘤抑制基因 GLIPR1 先前已被证实约有 10%的骨髓瘤患者发生缺失,可抑制老年小鼠浆细胞瘤的发展,且在轻链淀粉样变性(一种骨髓瘤相关恶性肿瘤)患者的浆细胞中表达水平降低。因此,我们假设 GLIPR1 可能在多发性骨髓瘤中具有肿瘤抑制活性。在这项研究中,我们证明了 GLIPR1 在大多数骨髓瘤患者中的浆细胞表达降低,并且 GLIPR1 在 5TGM1 鼠骨髓瘤细胞系中表达缺失。然而,在人骨髓瘤细胞系中过表达 GLIPR1 并不影响体外细胞增殖。同样,在 5TGM1 细胞中重新表达 Glipr1 也不能显著降低其体外增殖或在 C57BL/KaLwRij 小鼠体内的生长。此外,我们使用 CRISPR-Cas9 基因组编辑技术生成了 C57BL/Glipr1-/- 小鼠,并表明体内 Glipr1 的缺失不会影响正常造血或这些小鼠在一岁之前单克隆浆细胞扩展的发展。综上所述,我们的结果表明 GLIPR1 不太可能是多发性骨髓瘤中的有效肿瘤抑制因子。然而,GLIPR1 的下调仍有可能与其他遗传病变协同作用,促进骨髓瘤的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee29/6988976/cdfcb40da4ae/pone.0228408.g001.jpg

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