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透明质酸片段逆转C6大鼠胶质瘤细胞系对替莫唑胺和卡莫司汀耐药性的能力。

The ability of hyaluronan fragments to reverse the resistance of C6 rat glioma cell line to temozolomide and carmustine.

作者信息

Karbownik Michał Seweryn, Pietras Tadeusz, Szemraj Janusz, Kowalczyk Edward, Nowak Jerzy Zygmunt

机构信息

Department of Pharmacology and Toxicology, Medical University of Lodz, Lodz, Poland.

Department of Pneumology and Allergology, Medical University of Lodz, Lodz, Poland.

出版信息

Contemp Oncol (Pozn). 2014;18(5):323-8. doi: 10.5114/wo.2014.43493. Epub 2014 Sep 23.

Abstract

AIM OF THE STUDY

Hyaluronan (HA) is an extracellular matrix (ECM) polymer that may contribute to the emergence of anti-cancer drug resistance. Attempts to reverse drug resistance using small hyaluronan oligomers (oHA) are being made. The initial reports suggest that the oHA fraction may effectively reverse anti-cancer drug resistance in glioma models. However, the reversal effects of oHA of defined molecular length on glioma cells have not been investigated yet. In this study, we examined HA fragments containing 2 disaccharide units (oHA-2), 5 disaccharide units (oHA-5), and 68 kDa hyaluronan polymer (HA-68k) as agents possibly reversing the resistance of a C6 rat glioma cell line to temozolomide (TMZ) and carmustine (BCNU).

MATERIAL AND METHODS

A 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) viability assay was used to assess the cytotoxicity of TMZ and BCNU in the presence or absence of the hyaluronan fragments. By comparing viability of the cells, the reversal effects of HA fragments on TMZ and BCNU resistance in C6 glioma cells were assessed.

RESULTS

We found statistically significant decreases in the viability of cells in the presence of TMZ+oHA-5 as compared to TMZ alone (51.2 ±4.5 vs. 74.2 ±5.8, p = 0.0031), BCNU+o-HA5 as compared to BCNU alone (49.3 ±4.4 vs. 65.6 ±5.7, p = 0.0119), and BCNU+HA-68k as compared to BCNU alone (55.2 ±2.3 vs. 65.6 ±5.7, p = 0.0496).

CONCLUSIONS

Hyaluronan oligomers of 5 disaccharide units (oHA-5) significantly reversed the resistance of C6 cells to TMZ and BCNU. The results are only preliminary and a more thorough follow-up investigation is required to assess their actual role.

摘要

研究目的

透明质酸(HA)是一种细胞外基质(ECM)聚合物,可能与抗癌药物耐药性的产生有关。目前正在尝试使用小透明质酸寡聚物(oHA)来逆转耐药性。初步报告表明,oHA部分可能有效逆转胶质瘤模型中的抗癌药物耐药性。然而,尚未研究确定分子长度的oHA对胶质瘤细胞的逆转作用。在本研究中,我们检测了含有2个二糖单位的HA片段(oHA-2)、5个二糖单位的HA片段(oHA-5)和68 kDa的透明质酸聚合物(HA-68k),它们可能是逆转C6大鼠胶质瘤细胞系对替莫唑胺(TMZ)和卡莫司汀(BCNU)耐药性的药物。

材料与方法

采用3-(4,5-二甲基-2-噻唑基)-2,5-二苯基-2H-四氮唑溴盐(MTT)活力测定法,评估在有无透明质酸片段存在的情况下TMZ和BCNU的细胞毒性。通过比较细胞活力,评估HA片段对C6胶质瘤细胞中TMZ和BCNU耐药性的逆转作用。

结果

我们发现,与单独使用TMZ相比,TMZ+oHA-5存在时细胞活力有统计学意义的下降(51.2±4.5对74.2±5.8,p =  0.0031);与单独使用BCNU相比,BCNU+o-HA5存在时细胞活力有统计学意义的下降(49.3±4.4对65.6±5.7,p = 0.0119);与单独使用BCNU相比,BCNU+HA-68k存在时细胞活力有统计学意义的下降(55.2±2.3对65.6±5.7,p = 0.0496)。

结论

5个二糖单位的透明质酸寡聚物(oHA-5)显著逆转了C6细胞对TMZ和BCNU的耐药性。这些结果只是初步的,需要更深入的后续研究来评估它们的实际作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6050/4248052/9f375339f4d6/WO-18-22909-g001.jpg

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