Campbell S C
Department of Urology, Northwestern University Medical School, Chicago, Illinois, USA.
J Urol. 1997 Nov;158(5):1663-74. doi: 10.1016/s0022-5347(01)64090-4.
Important advances in angiogenesis research are reviewed along with recent data implicating angiogenesis in the pathogenesis of urological malignancies.
The current understanding of angiogenesis and its importance in tumor biology is summarized. The rationale for anti-angiogenic therapy is reviewed and the clinical experience with these agents is discussed. An extensive literature search of angiogenesis in urological malignancies was performed.
Quantitative immunohistochemistry for endothelial antigens suggests that, as is the case with many other tumors, induction of angiogenesis contributes to the malignant phenotype of prostate and bladder carcinomas. Anti-angiogenic agents have demonstrated efficacy against urological tumors in experimental systems, and recent data suggest that these agents may also be useful for chemoprophylactic purposes. Putative angiogenesis inducers specific for each of the major urological malignancies have been identified. Quantitation of the expression of angiogenesis inducers and estimation of microvessel density have demonstrated prognostic value for urological malignancies.
The available data indicate that angiogenesis has an important role in the progression and metastasis of urological malignancies. Preclinical data coupled with experience in other cancers indicate that combining anti-angiogenic therapy with conventional treatment modalities has the potential to improve dramatically our management of these malignancies. Further research will be needed to define the mechanisms controlling angiogenesis in urological malignancies and to determine if any of the angiogenic correlates will be of genuine clinical use. The rapid pace of research in this field suggests that this aspect of tumor biology will soon have an increasingly important role in the evaluation and treatment of urological cancers.
回顾血管生成研究的重要进展以及近期有关血管生成在泌尿生殖系统恶性肿瘤发病机制中作用的数据。
总结了目前对血管生成及其在肿瘤生物学中重要性的认识。回顾了抗血管生成治疗的基本原理并讨论了这些药物的临床经验。对泌尿生殖系统恶性肿瘤中的血管生成进行了广泛的文献检索。
内皮抗原的定量免疫组化表明,与许多其他肿瘤一样,血管生成的诱导有助于前列腺癌和膀胱癌的恶性表型。抗血管生成药物在实验系统中已显示出对泌尿生殖系统肿瘤的疗效,近期数据表明这些药物也可能用于化学预防目的。已确定了针对每种主要泌尿生殖系统恶性肿瘤的假定血管生成诱导剂。血管生成诱导剂表达的定量和微血管密度的估计已显示出对泌尿生殖系统恶性肿瘤的预后价值。
现有数据表明血管生成在泌尿生殖系统恶性肿瘤的进展和转移中起重要作用。临床前数据以及在其他癌症中的经验表明,将抗血管生成治疗与传统治疗方式相结合有可能显著改善我们对这些恶性肿瘤的管理。需要进一步研究来确定控制泌尿生殖系统恶性肿瘤中血管生成的机制,并确定是否有任何血管生成相关因素具有真正的临床应用价值。该领域的快速研究步伐表明,肿瘤生物学的这一方面将很快在泌尿生殖系统癌症的评估和治疗中发挥越来越重要的作用。