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SLC6A4 表达与血清素转运体配体氯米帕明和氟西汀对原发性 B 细胞恶性肿瘤的抗增殖反应。

SLC6A4 expression and anti-proliferative responses to serotonin transporter ligands chlomipramine and fluoxetine in primary B-cell malignancies.

机构信息

MRC Centre for Immune Regulation, The Medical School, Vincent Drive, Birmingham B15 2TT, UK.

出版信息

Leuk Res. 2010 Aug;34(8):1103-6. doi: 10.1016/j.leukres.2010.03.007. Epub 2010 Apr 2.

Abstract

B-cell lines of diverse neoplastic origin express the serotonin transporter (SERT/SLC6A4) and growth arrest in response to SERT-ligands, including the antidepressants chlomipramine and fluoxetine. Here we detail SLC6A4 transcript (Q-PCR) and protein (FACS) expression in primary cells from patients with: chronic lymphocytic leukaemia; mantle cell lymphoma; follicular lymphoma; Burkitt's lymphoma; and diffuse large B-cell lymphoma. The ability of the SERT-binding antidepressants to impact the growth of these cells when sustained on CD154-transfected fibroblasts was also determined. The results reveal a broad spectrum of primary B-cell malignancies expressing SLC6A4 with a proportion additionally displaying growth arrest on SERT-ligand exposure.

摘要

不同肿瘤来源的 B 细胞系表达血清素转运体(SERT/SLC6A4),并对 SERT 配体(包括抗抑郁药氯米帕明和氟西汀)产生生长抑制反应。在此,我们详细描述了慢性淋巴细胞白血病、套细胞淋巴瘤、滤泡性淋巴瘤、伯基特淋巴瘤和弥漫性大 B 细胞淋巴瘤患者原代细胞中的 SLC6A4 转录本(Q-PCR)和蛋白(FACS)表达。还确定了 SERT 结合型抗抑郁药在持续转染 CD154 的成纤维细胞上对这些细胞生长的影响。结果显示,广泛表达 SLC6A4 的原发性 B 细胞恶性肿瘤,其中一部分在 SERT 配体暴露时显示出生长抑制。

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