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杂合脂质体抑制原发性渗出性淋巴瘤的体外和体内生长。

Hybrid liposomes inhibit the growth of primary effusion lymphoma in vitro and in vivo.

机构信息

Division of Applied Life Science, Graduate School of Engineering, Sojo University, Kumamoto, Japan.

出版信息

Leuk Res. 2010 Jul;34(7):906-11. doi: 10.1016/j.leukres.2009.12.010. Epub 2010 Jan 13.

Abstract

Primary effusion lymphoma (PEL) is an aggressive neoplasm caused by Kaposi sarcoma-associated herpesvirus/human herpesvirus 8 (KSHV/HHV-8) infection. It occurs predominantly in human immunodeficiency virus (HIV)-positive patients, is generally resistant to chemotherapy, and has a poor prognosis. Hybrid liposomes (HL), composed of dimyristoylphosphatidylcholine (DMPC) and polyoxyethylene dodecyl ether, inhibited PEL cell proliferation and induced apoptosis in vitro. Intraperitoneal inoculation of the BCBL-1 PEL cell line into NOD/Scid/Jak3 deficient mice induced massive ascites, which were inhibited by HL21 without significant systemic toxicity in the mice. These results suggest that HL21 is an effective and attractive reagent for PEL treatment.

摘要

原发性渗出性淋巴瘤 (PEL) 是一种由卡波西肉瘤相关疱疹病毒/人类疱疹病毒 8 (KSHV/HHV-8) 感染引起的侵袭性肿瘤。它主要发生在人类免疫缺陷病毒 (HIV) 阳性患者中,通常对化疗有抵抗力,预后不良。由二肉豆蔻酰磷脂酰胆碱 (DMPC) 和聚氧乙烯十二烷基醚组成的杂交脂质体 (HL) 在体外抑制 PEL 细胞增殖并诱导细胞凋亡。将 PEL 细胞系 BCBL-1 腹腔接种入 NOD/Scid/Jak3 缺陷型小鼠中会诱导大量腹水,HL21 可抑制腹水形成,而小鼠无明显全身毒性。这些结果表明 HL21 是一种治疗 PEL 的有效且有吸引力的试剂。

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