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蛋白酶体抑制剂可阻止与HHV-8无关的PEL样淋巴瘤中的肿瘤细胞增殖。

Proteasome inhibitors prevent tumor cell proliferation in HHV-8-unrelated PEL-like lymphoma.

作者信息

Kawauchi Kiyotaka, Ogasawara Toshie

机构信息

Tokyo Women's Medical University, Adachi Medical Center, Department of Medicine, 4-33-1 Kohoku Adachi-ku, Tokyo, Japan.

出版信息

Leuk Res Rep. 2024 Dec 19;23:100497. doi: 10.1016/j.lrr.2024.100497. eCollection 2025.

DOI:10.1016/j.lrr.2024.100497
PMID:39845338
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11750559/
Abstract

Primary effusion lymphoma (PEL)-like lymphoma is a rare variant of PEL that exhibits diverse clinical behaviors, ranging from mild to aggressive disease courses. The clinicopathological features and effective treatments for this type of lymphoma have not been well defined. We found that proteasome inhibitors were effective in inhibiting the growth and survival of OGU1 cells, which were derived from a patient with aggressive PEL-like lymphoma, highlighting the critical role of proteasome activity in the proliferation of PEL-like lymphoma cells. This suggests that proteasome inhibitors, such as bortezomib, could be promising therapeutic options for patients who respond poorly to conventional chemotherapy.

摘要

原发性渗出性淋巴瘤(PEL)样淋巴瘤是PEL的一种罕见变体,表现出从轻度到侵袭性病程的多种临床行为。这种类型淋巴瘤的临床病理特征和有效治疗方法尚未明确界定。我们发现蛋白酶体抑制剂可有效抑制OGU1细胞的生长和存活,OGU1细胞源自一名侵袭性PEL样淋巴瘤患者,这突出了蛋白酶体活性在PEL样淋巴瘤细胞增殖中的关键作用。这表明蛋白酶体抑制剂,如硼替佐米,对于对传统化疗反应不佳的患者可能是有前景的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b0/11750559/933f904e24c6/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b0/11750559/933f904e24c6/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b0/11750559/933f904e24c6/gr1.jpg

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Proteasome inhibitors prevent tumor cell proliferation in HHV-8-unrelated PEL-like lymphoma.蛋白酶体抑制剂可阻止与HHV-8无关的PEL样淋巴瘤中的肿瘤细胞增殖。
Leuk Res Rep. 2024 Dec 19;23:100497. doi: 10.1016/j.lrr.2024.100497. eCollection 2025.
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The proteasome inhibitor bortezomib (PS-341) inhibits growth and induces apoptosis in primary effusion lymphoma cells.蛋白酶体抑制剂硼替佐米(PS-341)可抑制原发性渗出性淋巴瘤细胞的生长并诱导其凋亡。
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本文引用的文献

1
Targeting VEGF with bevacizumab inhibits malignant effusion formation of primary human herpesvirus 8-unrelated effusion large B-cell lymphoma in vivo.贝伐珠单抗靶向血管内皮生长因子抑制体内原发性人类疱疹病毒 8 无关渗出性大 B 细胞淋巴瘤的恶性渗出形成。
J Cell Mol Med. 2022 Nov;26(22):5580-5589. doi: 10.1111/jcmm.17570. Epub 2022 Oct 9.
2
Establishment and characterization of a novel VEGF-producing HHV-8-unrelated PEL-like lymphoma cell line, OGU1.新型产生血管内皮生长因子的与卡波西肉瘤相关疱疹病毒无关的原发性渗出性淋巴瘤样淋巴瘤细胞系OGU1的建立与鉴定
Eur J Haematol. 2016 Feb;96(2):144-51. doi: 10.1111/ejh.12559. Epub 2015 Apr 21.
3
Bortezomib-based therapy for newly diagnosed mantle-cell lymphoma.
硼替佐米为基础的治疗新诊断的套细胞淋巴瘤。
N Engl J Med. 2015 Mar 5;372(10):944-53. doi: 10.1056/NEJMoa1412096.
4
Human herpesvirus 8-unrelated primary effusion lymphoma-like lymphoma: report of a rare case and review of 54 cases in the literature.人疱疹病毒 8 无关原发性渗出性淋巴瘤样淋巴瘤:1 例罕见病例报告及文献复习 54 例。
Am J Clin Pathol. 2013 Aug;140(2):258-73. doi: 10.1309/AJCPHZ3CHO4HUWET.
5
KSHV/HHV8-negative effusion-based lymphoma, a distinct entity associated with fluid overload states.基于 KSHV/HHV8 阴性渗出液的淋巴瘤,一种与液体超负荷状态相关的独特实体。
Am J Surg Pathol. 2013 Feb;37(2):241-9. doi: 10.1097/PAS.0b013e318267fabc.
6
Efficacy of bortezomib in a direct xenograft model of primary effusion lymphoma.硼替佐米在原发性渗出性淋巴瘤直接异种移植模型中的疗效。
Proc Natl Acad Sci U S A. 2010 Jul 20;107(29):13069-74. doi: 10.1073/pnas.1002985107. Epub 2010 Jul 6.
7
Regulation and importance of the PI3K/Akt/mTOR signaling pathway in hematologic malignancies.PI3K/Akt/mTOR 信号通路在血液系统恶性肿瘤中的调控作用及其重要性。
Anticancer Agents Med Chem. 2009 Nov;9(9):1024-38. doi: 10.2174/187152009789377772.
8
Proteasome inhibitor MG-132 mediated expression of p27Kip1 via S-phase kinase protein 2 degradation induces cell cycle coupled apoptosis in primary effusion lymphoma cells.蛋白酶体抑制剂MG-132通过降解S期激酶蛋白2介导p27Kip1的表达,从而诱导原发性渗出性淋巴瘤细胞发生细胞周期偶联凋亡。
Leuk Lymphoma. 2009 Jul;50(7):1204-13. doi: 10.1080/10428190902951799.