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苏拉明和DL-α-二氟甲基鸟氨酸对多胺代谢的相反作用有助于它们在体外对B16黑色素瘤细胞生长产生协同作用。

Opposing effects of suramin and DL-alpha-difluoromethylornithine on polyamine metabolism contribute to a synergistic action on B16 melanoma cell growth in vitro.

作者信息

Gritli-Linde A, Björkman U, Delle U, Hultborn R, Johansson B R, Nannmark U, Linde A

机构信息

Department of Oral Biochemistry, Göteborg University, Sweden.

出版信息

Anticancer Res. 1998 Mar-Apr;18(2A):863-70.

PMID:9615733
Abstract

Polyamines are crucial for normal and neoplastic cell growth. Treatment with the polyanionic drug suramin has pronounced antigrowth activity in several tumor cell lines, but its clinical use has been hampered by its toxicity. We have earlier shown that suramin affects cellular polyamine metabolism and transport, and that these effects were, in some respects, opposite to those of alpha-difluoromethylomithine (DFMO), a specific inhibitor to ornithine decarboxylase, a key metabolic enzyme for polyamines. DFMO has been used in anticancer trials, although with limited success. Combinations of suramin and DFMO were, hence, evaluated in vitro and were found to strongly inhibit B16 melanoma cell proliferation. DFMO alone induced melanoma cell differentiation, and suramin used in combination with DFMO did not abrogate this DFMO-induced differentiation. Synergy analysis demonstrated a pronounced growth-inhibitory synergism between suramin and DFMO. The results suggest that the efficacy of combinations of DFMO with suramin or its analogues should be further explored, especially in cells requiring high levels of polyamines for their growth.

摘要

多胺对于正常细胞和肿瘤细胞的生长至关重要。用聚阴离子药物苏拉明处理在几种肿瘤细胞系中具有明显的抗生长活性,但其临床应用因毒性而受到阻碍。我们之前已经表明,苏拉明会影响细胞多胺代谢和转运,并且这些作用在某些方面与α-二氟甲基鸟氨酸(DFMO)相反,DFMO是鸟氨酸脱羧酶(一种多胺关键代谢酶)的特异性抑制剂。DFMO已用于抗癌试验,尽管成效有限。因此,对苏拉明和DFMO的组合进行了体外评估,发现其能强烈抑制B16黑色素瘤细胞增殖。单独使用DFMO可诱导黑色素瘤细胞分化,而与DFMO联合使用的苏拉明并未消除这种由DFMO诱导的分化。协同分析表明苏拉明和DFMO之间存在明显的生长抑制协同作用。结果表明,应进一步探索DFMO与苏拉明或其类似物组合的疗效,尤其是在生长需要高水平多胺的细胞中。

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