Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, Pennsylvania.
Pathology and Laboratory Medicine, Penn State Hershey Medical Center, Hershey, Pennsylvania.
Cancer Res. 2017 Apr 15;77(8):1942-1954. doi: 10.1158/0008-5472.CAN-16-1084. Epub 2017 Feb 15.
Little is known about how megakaryocytes may affect metastasis beyond serving as a source of platelets. In this study, we explored the functional implications of megakaryocyte accumulation in the femurs of mice after injection of metastatic or non-metastatic breast cancer cells in 4T1.2 BALB/cJ and MDA-MB-231 nude mouse models. At bone metastatic sites, but not primary growth sites, tumor growth was associated with increased megakaryopoiesis in both model systems. In the orthotopic BALB/cJ model, extramedullary hematopoiesis occurred in the spleen, resulting in a four-fold increase in megakaryocytes. In support of the hypothesis that reducing megakaryocytes may reduce metastasis, we found that thrombopoietin-deficient mice exhibited a 90% relative decrease in megakaryocytes, yet they developed more aggressive metastasis than wild-type hosts. In human clinical specimens, we observed an increase in megakaryocytes in the bone marrow of 6/8 patients with metastatic breast cancer compared with age- and gender-matched controls. Taken together, our results suggested that an increase in megakaryocytes occurring in response to metastatic cells entering the bone marrow confers some measure of protection against metastasis, challenging present views on the role of megakaryocytes in this setting. .
目前对于巨核细胞如何影响转移(除了作为血小板的来源之外)知之甚少。在这项研究中,我们在 4T1.2 BALB/cJ 和 MDA-MB-231 裸鼠模型中探索了转移性或非转移性乳腺癌细胞注射后小鼠股骨中巨核细胞积累的功能意义。在骨转移部位,但不在原发性生长部位,肿瘤生长与两种模型系统中巨核细胞生成的增加有关。在原位 BALB/cJ 模型中,骨髓外造血发生在脾脏中,导致巨核细胞增加了四倍。为了支持减少巨核细胞可能减少转移的假设,我们发现血小板生成素缺陷小鼠的巨核细胞减少了 90%,但它们比野生型宿主发展出更具侵袭性的转移。在人类临床标本中,我们观察到 6/8 例转移性乳腺癌患者的骨髓中巨核细胞增加,与年龄和性别匹配的对照组相比。总之,我们的结果表明,转移性细胞进入骨髓时发生的巨核细胞增加为转移提供了一定程度的保护,这对目前关于巨核细胞在这种情况下的作用的观点提出了挑战。