Possible effects of plasminogen activator inhibitor-1 on promoting angiogenesis through matrix metalloproteinase 9 in advanced mycosis fungoides

IF 3.3 4区 医学 Q2 HEMATOLOGY
Taku Fujimura, Kentaro Ohuchi, Tetsuya Ikawa, Yumi Kambayashi, Ryo Amagai, Sadanori Furudate, Yoshihide Asano
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引用次数: 0

Abstract

Mycosis fungoides (MF) progresses slowly before advancing to skin tumors followed by lymph node and visceral involvement. Among MF progression, stage IIB is an initial time point of tumor formation in MF. Since MF in tumor stage possess abundant blood vessels, it is important to evaluate the pro-angiogenic factors before and after MF in stage IIB. In this report, we investigated pro-angiogenic soluble factors in MF patients, as well as its pro-angiogenetic effects on tumor cells and stroma cells. We first evaluated the serum levels of pro-angiogenic factors in 9 MF patients without tumor formation and 8 MF patients with tumor formation. Among them, the serum MMP-9 and plasminogen activator inhibitors 1 (PAI-1) was significantly increased in MF with tumor formation compared in MF without tumor formation, leading to favorable formation of human dermal microvascular endothelial cells tube networks. Moreover, PAI-1 stimulation significantly increased the mRNA expression and protein production MMP-9 on monocytes derived M2 macrophages and HUT-78. Furthermore, since MMP-9 production from tumor cells as well as stromal cells is suppressed by bexarotene, we evaluate the baseline serum pro-angiogenic factors including MMP-9 in 16 patients with advanced cutaneous T cell lymphoma treated with bexarotene. The serum levels of MMP-2 and MMP-9 was significantly increased in bexarotene non-responded patients compared to responded patients. Our present study suggested the significance of MMP-9 and PAI-1 for the progression of MF stage toward to the tumor stage, and could be a therapeutic target in future.

浆细胞酶原激活物抑制剂-1通过基质金属蛋白酶9促进晚期真菌病血管生成的可能作用
放线菌病(MF)进展缓慢,随后发展为皮肤肿瘤,继而累及淋巴结和内脏。在真菌病的进展过程中,IIB期是真菌病肿瘤形成的初始时间点。由于肿瘤期的 MF 具有丰富的血管,因此评估 MF IIB 期前后的促血管生成因子非常重要。在本报告中,我们研究了 MF 患者的促血管生成可溶性因子及其对肿瘤细胞和基质细胞的促血管生成作用。我们首先评估了 9 名未形成肿瘤的 MF 患者和 8 名形成肿瘤的 MF 患者血清中促血管生成因子的水平。其中,与未形成肿瘤的 MF 相比,形成肿瘤的 MF 患者血清中 MMP-9 和纤溶酶原激活物抑制剂 1(PAI-1)明显升高,这有利于人体真皮微血管内皮细胞管网的形成。此外,PAI-1 刺激可显著增加单核细胞衍生的 M2 巨噬细胞和 HUT-78 上 MMP-9 的 mRNA 表达和蛋白生成。此外,由于贝沙罗汀可抑制肿瘤细胞和基质细胞产生 MMP-9,我们对 16 名接受贝沙罗汀治疗的晚期皮肤 T 细胞淋巴瘤患者进行了血清促血管生成因子(包括 MMP-9)基线评估。与有反应的患者相比,贝沙罗汀无反应患者血清中的 MMP-2 和 MMP-9 水平明显升高。本研究表明,MMP-9和PAI-1对MF期向肿瘤期的进展具有重要意义,可作为未来的治疗靶点。
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来源期刊
Hematological Oncology
Hematological Oncology 医学-血液学
CiteScore
4.20
自引率
6.10%
发文量
147
审稿时长
>12 weeks
期刊介绍: Hematological Oncology considers for publication articles dealing with experimental and clinical aspects of neoplastic diseases of the hemopoietic and lymphoid systems and relevant related matters. Translational studies applying basic science to clinical issues are particularly welcomed. Manuscripts dealing with the following areas are encouraged: -Clinical practice and management of hematological neoplasia, including: acute and chronic leukemias, malignant lymphomas, myeloproliferative disorders -Diagnostic investigations, including imaging and laboratory assays -Epidemiology, pathology and pathobiology of hematological neoplasia of hematological diseases -Therapeutic issues including Phase 1, 2 or 3 trials as well as allogeneic and autologous stem cell transplantation studies -Aspects of the cell biology, molecular biology, molecular genetics and cytogenetics of normal or diseased hematopoeisis and lymphopoiesis, including stem cells and cytokines and other regulatory systems. Concise, topical review material is welcomed, especially if it makes new concepts and ideas accessible to a wider community. Proposals for review material may be discussed with the Editor-in-Chief. Collections of case material and case reports will be considered only if they have broader scientific or clinical relevance.
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