Department of Applied Life Science, The Graduate School, Yonsei University, Seoul, South Korea.
BK21 Four Project, Yonsei University College of Dentistry, Seoul, South Korea.
Front Immunol. 2021 Dec 15;12:807600. doi: 10.3389/fimmu.2021.807600. eCollection 2021.
Cancer tissues are not just simple masses of malignant cells, but rather complex and heterogeneous collections of cellular and even non-cellular components, such as endothelial cells, stromal cells, immune cells, and collagens, referred to as tumor microenvironment (TME). These multiple players in the TME develop dynamic interactions with each other, which determines the characteristics of the tumor. Platelets are the smallest cells in the bloodstream and primarily regulate blood coagulation and hemostasis. Notably, cancer patients often show thrombocytosis, a status of an increased platelet number in the bloodstream, as well as the platelet infiltration into the tumor stroma, which contributes to cancer promotion and progression. Thus, platelets function as one of the important stromal components in the TME, emerging as a promising chemotherapeutic target. However, the use of traditional antiplatelet agents, such as aspirin, has limitations mainly due to increased bleeding complications. This requires to implement new strategies to target platelets for anti-cancer effects. In oral squamous cell carcinoma (OSCC) patients, both high platelet counts and low tumor-stromal ratio (high stroma) are strongly correlated with increased metastasis and poor prognosis. OSCC tends to invade adjacent tissues and bones and spread to the lymph nodes for distant metastasis, which is a huge hurdle for OSCC treatment in spite of relatively easy access for visual examination of precancerous lesions in the oral cavity. Therefore, locoregional control of the primary tumor is crucial for OSCC treatment. Similar to thrombocytosis, higher expression of podoplanin (PDPN) has been suggested as a predictive marker for higher frequency of lymph node metastasis of OSCC. Cumulative evidence supports that platelets can directly interact with PDPN-expressing cancer cells C-type lectin-like receptor 2 (CLEC2), contributing to cancer cell invasion and metastasis. Thus, the platelet CLEC2-PDPN axis could be a pinpoint target to inhibit interaction between platelets and OSCC, avoiding undesirable side effects. Here, we will review the role of platelets in cancer, particularly focusing on CLEC2-PDPN interaction, and will assess their potentials as therapeutic targets for OSCC treatment.
肿瘤组织不仅仅是恶性细胞的简单聚集,而是由多种细胞甚至非细胞成分组成的复杂异质集合,如内皮细胞、基质细胞、免疫细胞和胶原,被称为肿瘤微环境(TME)。TME 中的这些多种参与者彼此之间形成动态相互作用,决定了肿瘤的特征。血小板是血液中最小的细胞,主要调节血液凝固和止血。值得注意的是,癌症患者常表现出血小板增多症,即血液中血小板数量增加,以及血小板浸润肿瘤基质,这有助于癌症的促进和进展。因此,血小板作为 TME 中的重要基质成分之一,成为有前途的化疗靶点。然而,传统抗血小板药物的应用,如阿司匹林,存在局限性,主要是由于出血并发症增加。这需要实施新的策略来靶向血小板以发挥抗癌作用。在口腔鳞状细胞癌(OSCC)患者中,高血小板计数和低肿瘤基质比(高基质)与增加转移和预后不良密切相关。OSCC 倾向于侵犯相邻组织和骨骼,并扩散到淋巴结进行远处转移,这对 OSCC 的治疗是一个巨大的障碍,尽管在口腔中进行癌前病变的肉眼检查相对容易。因此,原发肿瘤的局部控制对 OSCC 的治疗至关重要。类似于血小板增多症,较高的 podoplanin(PDPN)表达已被认为是 OSCC 淋巴结转移频率较高的预测标志物。越来越多的证据支持血小板可以直接与表达 PDPN 的癌细胞 C 型凝集素样受体 2(CLEC2)相互作用,促进癌细胞侵袭和转移。因此,血小板 CLEC2-PDPN 轴可能是抑制血小板与 OSCC 相互作用的精确靶点,避免不良的副作用。在这里,我们将回顾血小板在癌症中的作用,特别是关注 CLEC2-PDPN 相互作用,并评估它们作为 OSCC 治疗的治疗靶点的潜力。