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仿生硫酸化糖胺聚糖维持乳腺上皮细胞的分化标志物,并优先抑制癌细胞的增殖。

Biomimetic sulfated glycosaminoglycans maintain differentiation markers of breast epithelial cells and preferentially inhibit proliferation of cancer cells.

作者信息

Habli Zeina, Deen Nataly Naser Al, Malaeb Waddah, Mahfouz Nadine, Mermerian Angela, Talhouk Rabih, Mhanna Rami

机构信息

Department of Biomedical Engineering, Maroun Semaan Faculty of Engineering and Architecture, American University of Beirut, Beirut, Beirut 1107 2020, Lebanon.

Department of Biology, Faculty of Arts and Sciences, American University of Beirut, Beirut, Beirut 1107 2020, Lebanon.

出版信息

Acta Biomater. 2021 Mar 1;122:186-198. doi: 10.1016/j.actbio.2020.12.049. Epub 2021 Jan 11.

Abstract

Glycosaminoglycans (GAG) are key elements involved in various physiological and pathological processes including cancer. Several GAG-based drugs have been developed showing significant results and potential use as cancer therapeutics. We previously reported that alginate sulfate (AlgSulf), a GAG-mimetic, reduces the proliferation of lung adenocarcinoma cells. In this study, we evaluated the preferential effect of AlgSulf on tumorigenic and nontumorigenic mammary epithelial cells in 2D, 3D, and coculture conditions. AlgSulf were synthesized with different degrees of sulfation (DSs) varying from 0 to 2.7 and used at 100 µg/mL on HMT-3522 S1 (S1) nontumorigenic mammary epithelial cells and their tumorigenic counterparts HMT-3522 T4-2 (T4-2) cells. The anti-tumor properties of AlgSulf were assessed using trypan blue and bromodeoxyuridine proliferation (BrdU) assays, immunofluorescence staining and transwell invasion assay.  Binding of insulin and epidermal growth factor (EGF) to sulfated substrates was measured using QCM-D and ELISA. In 2D, the cell growth rate of cells treated with AlgSulf was consistently lower compared to untreated controls (p<0.001) and surpassed the effect of the native GAG heparin (positive control). In 3D, AlgSulf preferentially hindered the growth rate and the invasion potential of tumorigenic T4-2 nodules while maintaining the formation of differentiated polarized nontumorigenic S1 acini. The preferential growth inhibition of tumorigenic cells by AlgSulf was confirmed in a coculture system (p<0.001). In the ELISA assay, a trend of EGF binding was detected for sulfated polysaccharides while QCM-D analysis showed negligible binding of insulin and EGF to sulfated substrates. The preferential effect mediated by the mimetic sulfated GAGs on cancer cells may in part be growth factor dependent. Our findings suggest a potential anticancer therapeutic role of AlgSulf for the development of anticancer drugs.

摘要

糖胺聚糖(GAG)是参与包括癌症在内的各种生理和病理过程的关键元素。已经开发出几种基于GAG的药物,显示出显著效果并具有作为癌症治疗药物的潜在用途。我们之前报道过,一种GAG模拟物硫酸藻酸盐(AlgSulf)可降低肺腺癌细胞的增殖。在本研究中,我们评估了AlgSulf在二维、三维和共培养条件下对致瘤性和非致瘤性乳腺上皮细胞的优先作用。合成了硫酸化程度(DS)从0到2.7不等的AlgSulf,并以100μg/mL的浓度用于HMT - 3522 S1(S1)非致瘤性乳腺上皮细胞及其致瘤性对应物HMT - 3522 T4 - 2(T4 - 2)细胞。使用台盼蓝和溴脱氧尿苷增殖(BrdU)测定、免疫荧光染色和Transwell侵袭测定来评估AlgSulf的抗肿瘤特性。使用石英晶体微天平检测(QCM - D)和酶联免疫吸附测定(ELISA)测量胰岛素和表皮生长因子(EGF)与硫酸化底物的结合。在二维条件下,与未处理的对照相比,用AlgSulf处理的细胞的生长速率持续较低(p<0.001),并且超过了天然GAG肝素(阳性对照)的作用。在三维条件下,AlgSulf优先阻碍致瘤性T4 - 2结节的生长速率和侵袭潜力,同时维持分化的极化非致瘤性S1腺泡的形成。在共培养系统中证实了AlgSulf对致瘤性细胞的优先生长抑制作用(p<0.001)。在ELISA测定中,检测到硫酸化多糖存在EGF结合趋势,而QCM - D分析显示胰岛素和EGF与硫酸化底物的结合可忽略不计。模拟硫酸化GAG介导的对癌细胞的优先作用可能部分依赖于生长因子。我们的研究结果表明AlgSulf在抗癌药物开发中具有潜在的抗癌治疗作用。

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