Lokman Noor A, Price Zoe K, Hawkins Emily K, Macpherson Anne M, Oehler Martin K, Ricciardelli Carmela
Discipline of Obstetrics and Gynaecology, Adelaide Medical School, Robinson Research Institute, University of Adelaide, Adelaide, SA 5000, Australia.
Department of Gynaecological Oncology, Royal Adelaide Hospital, Adelaide, SA 5005, Australia.
Cancers (Basel). 2019 Aug 15;11(8):1187. doi: 10.3390/cancers11081187.
We have recently shown that the extracellular matrix molecule hyaluronan (HA) plays a role in the development of ovarian cancer chemoresistance. This present study determined if HA production is increased in chemotherapy-resistant ovarian cancers and if the HA inhibitor 4-methylubelliferone (4-MU) can overcome chemoresistance to the chemotherapeutic drug carboplatin (CBP) and inhibit spheroid formation and the expression of cancer stem cell (CSC) markers. We additionally assessed whether 4-MU could inhibit in vivo invasion of chemoresistant primary ovarian cancer cells in the chicken embryo chorioallantoic membrane (CAM) assay. The expression of the HA synthases and was significantly increased in chemoresistant compared to chemosensitive primary ovarian cancer cells isolated from patient ascites. 4-MU significantly inhibited HA production, cell survival, and spheroid formation of chemoresistant serous ovarian cancer cells. In combination with CBP, 4-MU treatment significantly decreased ovarian cancer cell survival and increased apoptosis of chemoresistant primary cells compared to CBP alone. 4-MU significantly reduced spheroid formation, expression of CSC markers and in primary cell spheroid cultures, and ALDH1 immunostaining in patient-derived tissue explant assays following treatment with CBP. Furthermore, 4-MU was very effective at inhibiting in vivo invasion of chemoresistant primary cells in CAM assays. Inhibition of HA is therefore a promising new strategy to overcome chemoresistance and to improve ovarian cancer survival.
我们最近发现,细胞外基质分子透明质酸(HA)在卵巢癌化疗耐药性的发展中起作用。本研究确定了化疗耐药的卵巢癌中HA的产生是否增加,以及HA抑制剂4-甲基伞形酮(4-MU)是否能克服对化疗药物卡铂(CBP)的耐药性,并抑制球体形成和癌症干细胞(CSC)标志物的表达。我们还评估了4-MU是否能在鸡胚绒毛尿囊膜(CAM)试验中抑制化疗耐药的原发性卵巢癌细胞的体内侵袭。与从患者腹水中分离出的化疗敏感的原发性卵巢癌细胞相比,化疗耐药细胞中HA合酶 和 的表达显著增加。4-MU显著抑制了化疗耐药的浆液性卵巢癌细胞的HA产生、细胞存活和球体形成。与CBP联合使用时,与单独使用CBP相比,4-MU治疗显著降低了卵巢癌细胞的存活率,并增加了化疗耐药的原代细胞的凋亡。在用CBP治疗后的原代细胞球体培养物中,4-MU显著减少了球体形成、CSC标志物 和 的表达,以及患者来源组织外植体试验中的ALDH1免疫染色。此外,在CAM试验中,4-MU在抑制化疗耐药原代细胞的体内侵袭方面非常有效。因此,抑制HA是一种有前景的新策略,可克服化疗耐药性并提高卵巢癌患者的生存率。