Dührsen U, Hossfeld D K
Abteilung für Onkologie und Hämatologie, Universitätskrankenhaus Eppendorf, Hamburg, Germany.
Ann Hematol. 1996 Aug;73(2):53-70. doi: 10.1007/s002770050203.
Bone marrow malignancies are clonal disorders resulting from neoplastic transformation of hematopoietic stem or progenitor cells. Similar to their normal counterparts, transformed blood-forming cells remain dependent on signals from the hematopoiesis-regulating stromal environment for survival and proliferation. There is increasing evidence that the microenvironment may also take a more active part in the disease process. A review of the literature on stromal abnormalities in the leukemias, the myelodysplastic syndromes, and multiple myeloma reveals three principal mechanisms by which stromal derangements can contribute to the evolution of a neoplastic disease. In the simplest case, neoplastic blood-forming cells induce reversible changes in stroma function or composition which result in improved growth conditions for the malignant cells ('malignancy-induced microenvironment'). In the second setting, functionally abnormal end cells derived from the malignant clone become an integral part of the stroma system, selectively stimulating the neoplastic cells and inhibiting normal blood cell formation ('malignant microenvironment'). In the third condition, the emergence of a neoplastic cell population is the consequence of a primary stroma lesion characterized by inability to control regular blood cell formation ('malignancy-inducing microenvironment'). The perception of different stroma-related disease mechanisms may eventually lead to the development of alternative therapeutic approaches.
骨髓恶性肿瘤是造血干细胞或祖细胞发生肿瘤转化而导致的克隆性疾病。与其正常对应细胞相似,转化后的造血细胞在生存和增殖方面仍依赖于造血调节性基质环境发出的信号。越来越多的证据表明,微环境可能在疾病过程中也发挥着更积极的作用。对有关白血病、骨髓增生异常综合征和多发性骨髓瘤中基质异常的文献进行综述后发现,基质紊乱可通过三种主要机制促进肿瘤性疾病的进展。在最简单的情况下,肿瘤性造血细胞会诱导基质功能或组成发生可逆性变化,从而为恶性细胞创造更好的生长条件(“恶性肿瘤诱导的微环境”)。在第二种情况下,源自恶性克隆的功能异常终末细胞成为基质系统的一个组成部分,选择性地刺激肿瘤细胞并抑制正常血细胞生成(“恶性微环境”)。在第三种情况下,肿瘤细胞群体的出现是原发性基质病变的结果,其特征是无法控制正常血细胞生成(“恶性肿瘤诱导微环境”)。对不同的基质相关疾病机制的认识最终可能会促成替代治疗方法的发展。