Kola Brusi, Kakkat Sooraj, Suman Prabhat, Crouch Emily, Chakroborty Debanjan, Sarkar Chandrani
Cancer Biology Program, Mitchell Cancer Institute, University of South Alabama, Mobile, Alabama, USA.
Department of Pathology, Frederick P. Whiddon College of Medicine, University of South Alabama, Mobile, Alabama, USA.
FASEB J. 2025 May 15;39(9):e70590. doi: 10.1096/fj.202500024R.
Despite the recent advances in treatment, breast cancer (BCa) remains a leading cause of cancer-related mortality worldwide, and metastasis accounts for the most significant number of BCa deaths. Lymphangiogenesis, the process by which new lymphatic vessels develop from pre-existing ones, is a major driver of BCa metastasis. High lymphatic vessel density is linked to lymph node metastasis and poor prognosis in BCa. Vascular endothelial growth factor receptor 3 (VEGFR3) and its ligands vascular endothelial growth factor C (VEGF-C) and VEGF-D have been described as key players in BCa-induced lymphangiogenesis. However, the molecular mechanisms associated with lymphangiogenesis in BCa are not fully understood. In this review, we discuss how the local breast tumor microenvironment modulates the process of lymphangiogenesis to facilitate disease progression and provide a mechanistic insight into the complex formation of lymphatic vessels in BCa, highlighting the role of the VEGF-C, D/VEGFR3 signaling axis, along with other molecular players. Additionally, the review discusses the versatile therapeutic potential targeting lymphangiogenesis in BCa and challenges that need to be overcome in the future. A complete understanding of lymphangiogenesis in BCa will open up new possibilities for targeted therapeutics that can potentially improve outcomes for BCa patients and the efficacy of current treatments.
尽管近年来在治疗方面取得了进展,但乳腺癌(BCa)仍是全球癌症相关死亡的主要原因,而转移是导致BCa死亡的最主要因素。淋巴管生成是指从已有的淋巴管发育出新的淋巴管的过程,是BCa转移的主要驱动因素。高淋巴管密度与BCa的淋巴结转移和不良预后相关。血管内皮生长因子受体3(VEGFR3)及其配体血管内皮生长因子C(VEGF-C)和VEGF-D被认为是BCa诱导的淋巴管生成的关键因子。然而,与BCa中淋巴管生成相关的分子机制尚未完全阐明。在本综述中,我们讨论了局部乳腺肿瘤微环境如何调节淋巴管生成过程以促进疾病进展,并对BCa中淋巴管的复杂形成提供了机制性见解,强调了VEGF-C、D/VEGFR3信号轴以及其他分子因子的作用。此外,本综述还讨论了针对BCa中淋巴管生成的多种治疗潜力以及未来需要克服的挑战。对BCa中淋巴管生成的全面理解将为靶向治疗开辟新的可能性,这有可能改善BCa患者的治疗效果和当前治疗的疗效。