Centre de Recherche en Cancérologie de Marseille, INSERM, CNRS, Aix-Marseille Université, Institut Paoli-Calmettes, Marseille, France.
INSERM, UMR_S1033, Université Claude Bernard Lyon-1, Lyon, France.
Br J Pharmacol. 2018 Aug;175(15):3100-3110. doi: 10.1111/bph.14362. Epub 2018 Jun 25.
Platelets play a crucial role in the survival of metastatic cells in the blood circulation. The interaction of tumour cells with platelets leads to the production of plethoric factors among which our review will focus on lysophosphatidic acid (LPA), because platelets are the highest producers of this bioactive lysophospholipid in the organism. LPA promotes platelet aggregation, and blocking platelet function decreases LPA signalling and leads to inhibition of breast cancer cell metastasis. Autotaxin (ATX), a lysophospholipase D responsible for the basal concentration of LPA in blood, was detected in platelet α-granules. Functionally, active ATX is eventually released following tumour cell-induced platelet aggregation, thereby promoting metastasis. Megakaryocytes do not express ATX but respond to LPA stimulation. Whether LPA-primed megakaryocytes contribute to the recently reported negative action of megakaryocytes on cancer metastasis is not yet known. However, an understanding of the ATX/LPA signalling pathways in platelets, cancer cells and megakaryocytes opens up new approaches for fighting cancer metastasis.
血小板在循环血液中转移性细胞的存活中起着至关重要的作用。肿瘤细胞与血小板的相互作用导致丰富因子的产生,其中我们的综述将重点关注溶血磷脂酸(LPA),因为血小板是生物体内这种生物活性溶血磷脂的最高产生者。LPA 促进血小板聚集,阻断血小板功能会降低 LPA 信号转导,从而抑制乳腺癌细胞转移。自分泌酶(ATX)是一种负责血液中 LPA 基础浓度的溶血磷脂酶 D,在血小板α-颗粒中被检测到。从功能上讲,在肿瘤细胞诱导的血小板聚集后,活性 ATX 最终被释放,从而促进转移。巨核细胞不表达 ATX,但对 LPA 刺激有反应。LPA 激活的巨核细胞是否有助于最近报道的巨核细胞对癌症转移的负性作用尚不清楚。然而,对血小板、癌细胞和巨核细胞中 ATX/LPA 信号通路的理解为对抗癌症转移开辟了新的途径。