Nekipelov Katrin, Nahain Abdullah Al, Otto Sven, Xu Yongbin, Li Jin-Ping, Letunica Natasha, Collett Simon, Attard Chantal, Monagle Paul, Vamvounis George, Tsanaktsidis John, Ferro Vito, Bendas Gerd
Department of Pharmacy, University of Bonn, An der Immenburg 4, 53121, Bonn, Germany.
School of Chemistry and Molecular Bioscience, University of Queensland, Brisbane, Queensland, 4072, Australia.
Macromol Biosci. 2025 Jul;25(7):e2400633. doi: 10.1002/mabi.202400633. Epub 2025 Apr 7.
Thromboses are potentially fatal complication in malignant tumor diseases. Today, oral anticoagulants are considered equivalent alternatives to low molecular weight heparin (LMWH) in guideline-based treatments of cancer-associated thromboses. Nevertheless, debates on potential antitumorigenic heparin activities beyond anticoagulation are still highly relevant. However, disclosure of heparin targeted activities is complicated by the heterogeneous structure of this glycosaminoglycan of natural origin. Therefore, synthetic polymers appear promising as heparin mimetics to interfere with different steps in tumor metastatic spread. Here, the synthesis of noncarbohydrate copolymers of itaconic acid is described with either potassium-3-sulfopropylmethacrylate (SPMA), sodium 4-styrenesulfonate (SS), or 2-acrylamido-2-methyl-1-propanesulfonate (AMPS) via reversible addition-fragmentation-chain-transfer (RAFT) polymerization. The copolymers, characterized by GPC, display high efficiencies to inhibit heparanase enzymatic activity, exceeding the potency of the clinical candidate PG545. The SS-copolymers (poly(SS-co-IA)) outperform the other copolymers and LMWH in blocking tumor cell-induced platelet activation (TCIPA), thus platelet degranulation or aggregation as key issues in metastasis by reducing thrombin formation. The cytotoxicity of poly(SS-co-IA) is very low. Notably, poly(SS-co-IA) copolymers displayed a thousand-fold lower binding affinity to platelet factor-4 (PF4) than unfractionated heparin (UFH), suggesting a lower risk for HIT II susceptibility. The indicated polymers represent promising heparin mimetics with superior activities in oncology for metastatic control.
血栓形成是恶性肿瘤疾病中潜在的致命并发症。如今,在基于指南的癌症相关血栓治疗中,口服抗凝剂被认为是低分子量肝素(LMWH)的等效替代品。然而,关于肝素抗凝以外潜在抗肿瘤活性的争论仍然高度相关。然而,由于这种天然来源的糖胺聚糖结构异质性,肝素靶向活性的揭示变得复杂。因此,合成聚合物作为肝素模拟物有望干扰肿瘤转移扩散的不同步骤。在此,描述了通过可逆加成-断裂链转移(RAFT)聚合,用3-磺丙基甲基丙烯酸钾(SPMA)、4-苯乙烯磺酸钠(SS)或2-丙烯酰胺-2-甲基-1-丙烷磺酸钠(AMPS)合成衣康酸的非碳水化合物共聚物。通过凝胶渗透色谱(GPC)表征的共聚物显示出高效抑制乙酰肝素酶活性,超过临床候选药物PG545的效力。SS共聚物(聚(SS-co-IA))在阻断肿瘤细胞诱导的血小板活化(TCIPA)方面优于其他共聚物和LMWH,从而通过减少凝血酶形成,使血小板脱颗粒或聚集成为转移中的关键问题。聚(SS-co-IA)的细胞毒性非常低。值得注意的是,聚(SS-co-IA)共聚物与血小板因子-4(PF4)的结合亲和力比未分级肝素(UFH)低一千倍,表明肝素诱导的血小板减少症(HIT II)易感性风险较低。所示聚合物代表了有前景的肝素模拟物,在肿瘤学中对转移控制具有卓越活性。