FAM19A5/S1PR1 signaling pathway regulates the viability and proliferation of mantle cell lymphoma.

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Receptors and Signal Transduction Pub Date : 2022-06-01 Epub Date: 2021-03-09 DOI:10.1080/10799893.2021.1895220
Yanfang Wang, Zhenhao Zhang, Wei Wan, Yan Liu, Hongmei Jing, Fei Dong
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引用次数: 2

Abstract

Several intracellular pathological processes have been reported to be regulated by the FAM19A5/S1PR1 signaling pathway. However, the role of FAM19A5/S1PR1 signaling pathway in the viability and proliferation of mantle cell lymphoma is not been completely understood. The task of this study is to explore the influence of FAM19A5/S1PR1 signaling pathway in affecting the survival and growth of mantle cell lymphoma. shRNAs against FAM19A5 or S1PR1 were transfected into mantle cell lymphom. Cell viability and proliferation were measured through MTT assay and CCK8 assay, respectively. Our results demonstrated that loss of FAM19A5 significantly reduced the viability of mantle cell lymphom, an effect that was followed by a drop in cell proliferation capacity. Besides, inhibition of S1PR1 also impairs cell survival and interrupt mantle cell lymphom proliferation in vitro. Taken together, our results illustrate that FAM19A5/S1PR1 signaling pathway is associated with the regulation of mantle cell lymphom viability and proliferation. This finding will provide a potential target for the treatment of malignant lymphoma in the clinical practice.

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FAM19A5/S1PR1信号通路调控套细胞淋巴瘤的生存和增殖。
据报道,FAM19A5/S1PR1信号通路可调节多种细胞内病理过程。然而,FAM19A5/S1PR1信号通路在套细胞淋巴瘤存活和增殖中的作用尚不完全清楚。本研究的任务是探讨FAM19A5/S1PR1信号通路对套细胞淋巴瘤存活和生长的影响。将针对FAM19A5或S1PR1的shrna转染到套细胞淋巴中。分别采用MTT法和CCK8法测定细胞活力和增殖能力。我们的研究结果表明,FAM19A5的缺失显著降低了套细胞淋巴细胞的活力,随后是细胞增殖能力的下降。此外,抑制S1PR1也会在体外损害细胞存活并中断套细胞淋巴细胞增殖。综上所述,我们的研究结果表明FAM19A5/S1PR1信号通路与套细胞淋巴细胞活力和增殖的调节有关。这一发现将为临床治疗恶性淋巴瘤提供一个潜在的靶点。
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来源期刊
Journal of Receptors and Signal Transduction
Journal of Receptors and Signal Transduction 生物-生化与分子生物学
CiteScore
6.60
自引率
0.00%
发文量
19
审稿时长
>12 weeks
期刊介绍: Journal of Receptors and Signal Tranduction is included in the following abstracting and indexing services: BIOBASE; Biochemistry and Biophysics Citation Index; Biological Abstracts; BIOSIS Full Coverage Shared; BIOSIS Previews; Biotechnology Abstracts; Current Contents/Life Sciences; Derwent Chimera; Derwent Drug File; EMBASE; EMBIOLOGY; Journal Citation Reports/ Science Edition; PubMed/MedLine; Science Citation Index; SciSearch; SCOPUS; SIIC.
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