Conditioned medium from normoxia (WJMSCs-norCM) and hypoxia-treated WJMSCs (WJMSCs-hypoCM) in inhibiting cancer cell proliferation

Wahyu Widowati , Laura Wijaya , Harry Murti , Halida Widyastuti , Dwi Agustina , Dian Ratih Laksmitawati , Nurul Fauziah , Sutiman B. Sumitro , M. Aris Widodo , Indra Bachtiar
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引用次数: 39

Abstract

Mesenchymal stem cells (MSCs) have unique properties, including high proliferation rates, self-renewal, multilineage differentiation ability, wide multipotency, hypoimmunogenicity, noninduction of teratomas, and anticancer properties. MSCs can be isolated from embryonic and extraembryonic tissues as well as adult organs. Human Wharton's jelly stem cell-conditioned medium possesses anticancer properties and inhibits the growth of solid tumors. Lower oxygen concentration or hypoxic condition can increase the proliferation of MSCs, but there are no differences in surface markers. We determined the osteocyte, chondrocyte, and adipocyte differentiation of normoxic WJMSCs (nor-WJMSCs) and hypoxic 2.5%, hypoxic 5% (hypo-WJMSCs); from a different passage (P4 and P8), we determined the inhibitory effect of WJMSCs-norCM and WJMSCs-hypoCM on the proliferation of human cancer cells including cervical (HeLa), liver (HepG2), prostate (pc3), ovarian (skov3), and oral squamous (hsc3) cancer cell lines compared to normal cells including mouse fibroblast (NIH3T3), human fibroblast, and human mesenchymal stem cells (hMSCs). Surfacer marker expression of nor-WJMSCs-and hypo-WJMSCs from P4 and P8 were >95% for CD90, CD73 and CD105 and <2% for CD14, CD19, CD34, CD45, and HLDA-II. Nor-WJMSCs and hypo-WJMSCs from P4 and P8 underwent differentiation to osteocyte, chondrocyte, and adipocyte. WJMSCs-norCM and WJMSCs-hypoCM could inhibit proliferation of various cancer cell lines with minimum inhibitory concentration (IC50) 51.690–81.440% and cause low inhibition of the normal cells with IC50 136.290–185.339%. WJMSCs-norCM and WJMSCs-hypoCM were not cytotoxic toward normal cells. Nor-WJMSCs and hypo-WJMSCs from P4 and P8 showed no significant differences in MSC surface marker expression or differentiation. WJMSCs-norCM and WJMSCs-hypoCM could inhibit proliferation in various cancer cell lines, and were safe for normal cells.

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常氧条件培养基(WJMSCs- norcm)和缺氧处理的WJMSCs (WJMSCs- hypocm)抑制癌细胞增殖的研究
间充质干细胞(MSCs)具有独特的特性,包括高增殖率、自我更新、多系分化能力、广泛的多能性、低免疫原性、不诱导畸胎瘤和抗癌特性。间充质干细胞可以从胚胎和胚胎外组织以及成人器官中分离出来。人类沃顿果冻干细胞条件培养基具有抗癌特性并抑制实体肿瘤的生长。较低氧浓度或缺氧条件可促进MSCs的增殖,但表面标志物无差异。我们测定了常氧WJMSCs(无WJMSCs)和缺氧2.5%、缺氧5%(低氧WJMSCs)的骨细胞、软骨细胞和脂肪细胞分化情况;通过不同的传代(P4和P8),我们测定了WJMSCs-norCM和WJMSCs-hypoCM与正常细胞(包括小鼠成纤维细胞(NIH3T3)、人成纤维细胞和人间充质干细胞(hMSCs))相比,对人宫颈癌(HeLa)、肝脏(HepG2)、前列腺(pc3)、卵巢(skov3)和口腔鳞状细胞(hsc3)的增殖抑制作用。来自P4和P8的非wjmscs和低wjmscs的表面标记表达为CD90、CD73和CD105的95%,CD14、CD19、CD34、CD45和hla - ii的2%。P4和P8的无wjmscs和低wjmscs分化为骨细胞、软骨细胞和脂肪细胞。WJMSCs-norCM和WJMSCs-hypoCM对多种癌细胞的增殖均有抑制作用,最低抑制浓度(IC50)为51.690 ~ 81.440%,对正常细胞的抑制作用较低,IC50为136.290 ~ 185.339%。WJMSCs-norCM和WJMSCs-hypoCM对正常细胞无细胞毒性。来自P4和P8的无wjmscs和低wjmscs在MSC表面标记物的表达和分化方面没有显著差异。WJMSCs-norCM和WJMSCs-hypoCM在多种癌细胞中均有抑制增殖的作用,对正常细胞是安全的。
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