Mukherjee Pritha, Zhou Xin, Benicky Julius, Panigrahi Aswini, Aljuhani Reem, Liu Jian, Ailles Laurie, Pomin Vitor H, Wang Zhangjie, Goldman Radoslav
Department of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20057, USA.
Biotechnology Program, Northern Virginia Community College, Manassas, VA 20109, USA.
Cancers (Basel). 2023 Oct 27;15(21):5168. doi: 10.3390/cancers15215168.
Local invasiveness of head and neck squamous cell carcinoma (HNSCC) is a complex phenomenon supported by interaction of the cancer cells with the tumor microenvironment (TME). We and others have shown that cancer-associated fibroblasts (CAFs) are a component of the TME that can promote local invasion in HNSCC and other cancers. Here we report that the secretory enzyme heparan-6--endosulfatase 2 (Sulf-2) directly affects the CAF-supported invasion of the HNSCC cell lines SCC35 and Cal33 into Matrigel. The Sulf-2 knockout (KO) cells differ from their wild type counterparts in their spheroid growth and formation, and the Sulf-2-KO leads to decreased invasion in a spheroid co-culture model with the CAF. Next, we investigated whether a fucosylated chondroitin sulfate isolated from the sea cucumber (HfFucCS) affects the activity of the Sulf-2 enzyme. Our results show that HfFucCS not only efficiently inhibits the Sulf-2 enzymatic activity but, like the Sulf-2 knockout, inhibits Matrigel invasion of SCC35 and Cal33 cells co-cultured with primary HNSCC CAF. These findings suggest that the heparan-6--endosulfatases regulate local invasion and could be therapeutically targeted with the inhibitory activity of a marine glycosaminoglycan.
头颈部鳞状细胞癌(HNSCC)的局部侵袭是一种复杂的现象,由癌细胞与肿瘤微环境(TME)的相互作用所支持。我们和其他人已经表明,癌症相关成纤维细胞(CAFs)是TME的一个组成部分,可促进HNSCC和其他癌症的局部侵袭。在此我们报告,分泌酶硫酸乙酰肝素-6-O-硫酸酯酶2(Sulf-2)直接影响CAF支持的HNSCC细胞系SCC35和Cal33向基质胶中的侵袭。Sulf-2基因敲除(KO)细胞在球状体生长和形成方面与其野生型对应物不同,并且在与CAF的球状体共培养模型中,Sulf-2-KO导致侵袭减少。接下来,我们研究了从海参中分离出的岩藻糖基化硫酸软骨素(HfFucCS)是否影响Sulf-2酶的活性。我们的结果表明,HfFucCS不仅有效抑制Sulf-2酶活性,而且与Sulf-2基因敲除一样,抑制与原发性HNSCC CAF共培养的SCC35和Cal33细胞对基质胶的侵袭。这些发现表明,硫酸乙酰肝素-6-O-硫酸酯酶调节局部侵袭,并且可以用海洋糖胺聚糖的抑制活性进行治疗靶向。