Mai Shaoshan, Inkielewicz-Stepniak Iwona
Department of Pharmaceutical Pathophysiology, Faculty of Pharmacy, Medical University of Gdańsk, Gdańsk, Poland.
Front Cell Dev Biol. 2021 Nov 10;9:749689. doi: 10.3389/fcell.2021.749689. eCollection 2021.
Platelets have been recognized as key players in hemostasis, thrombosis, and cancer. Preclinical and clinical researches evidenced that tumorigenesis and metastasis can be promoted by platelets through a wide variety of crosstalk between cancer cells and platelets. Pancreatic cancer is a devastating disease with high morbidity and mortality worldwide. Although the relationship between pancreatic cancer and platelets in clinical diagnosis is described, the interplay between pancreatic cancer and platelets, the underlying pathological mechanism and pathways remain a matter of intensive study. This review summaries recent researches in connections between platelets and pancreatic cancer. The existing data showed different underlying mechanisms were involved in their complex crosstalk. Typically, pancreatic tumor accelerates platelet aggregation which forms thrombosis. Furthermore, extracellular vesicles released by platelets promote communication in a neoplastic microenvironment and illustrate how these interactions drive disease progression. We also discuss the advantages of novel model organoids in pancreatic cancer research. A more in-depth understanding of tumor and platelets crosstalk which is based on organoids and translational therapies may provide potential diagnostic and therapeutic strategies for pancreatic cancer progression.
血小板已被公认为止血、血栓形成和癌症中的关键因素。临床前和临床研究证明,血小板可通过癌细胞与血小板之间的多种相互作用促进肿瘤发生和转移。胰腺癌是一种在全球范围内发病率和死亡率都很高的毁灭性疾病。尽管描述了胰腺癌与血小板在临床诊断中的关系,但胰腺癌与血小板之间的相互作用、潜在的病理机制和途径仍是深入研究的课题。本综述总结了血小板与胰腺癌之间联系的最新研究。现有数据表明,它们复杂的相互作用涉及不同的潜在机制。典型的情况是,胰腺肿瘤会加速血小板聚集,从而形成血栓。此外,血小板释放的细胞外囊泡促进肿瘤微环境中的通讯,并阐明这些相互作用如何推动疾病进展。我们还讨论了新型类器官模型在胰腺癌研究中的优势。基于类器官和转化疗法对肿瘤与血小板相互作用的更深入理解,可能为胰腺癌进展提供潜在的诊断和治疗策略。