School of Health & Life Sciences, Teesside University, Middlesbrough, TS1 3BX, UK.
National Horizons Centre, Teesside University, 38 John Dixon Ln, Darlington, DL1 1HG, UK.
Oncogene. 2020 Mar;39(10):2040-2054. doi: 10.1038/s41388-019-1124-8. Epub 2019 Dec 4.
Midkine is a heparin-binding growth factor, originally reported as the product of a retinoic acid-responsive gene during embryogenesis, but currently viewed as a multifaceted factor contributing to both normal tissue homeostasis and disease development. Midkine is abnormally expressed at high levels in various human malignancies and acts as a mediator for the acquisition of critical hallmarks of cancer, including cell growth, survival, metastasis, migration, and angiogenesis. Several studies have investigated the role of midkine as a cancer biomarker for the detection, prognosis, and management of cancer, as well as for monitoring the response to cancer treatment. Moreover, several efforts are also being made to elucidate its underlying mechanisms in therapeutic resistance and immunomodulation within the tumor microenvironment. We hereby summarize the current knowledge on midkine expression and function in cancer development and progression, and highlight its promising potential as a cancer biomarker and as a future therapeutic target in personalized cancer medicine.
中期因子是一种肝素结合生长因子,最初被报道为胚胎发生过程中视黄酸反应基因的产物,但目前被认为是一种多功能因子,有助于正常组织稳态和疾病的发展。中期因子在多种人类恶性肿瘤中异常高表达,并作为获得癌症关键特征的介质,包括细胞生长、存活、转移、迁移和血管生成。多项研究调查了中期因子作为癌症生物标志物在癌症的检测、预后和管理以及监测癌症治疗反应中的作用。此外,还在努力阐明其在肿瘤微环境中的治疗耐药性和免疫调节中的潜在机制。在此,我们总结了中期因子在癌症发生和发展过程中的表达和功能的现有知识,并强调了其作为癌症生物标志物和个性化癌症医学中未来治疗靶点的有前途的潜力。