Investigative strategies on lymphatic vessel modulation for treating lymphedema in future medicine Journal Article
| Authors: | Kataru, R. P.; Mehrara, B. J.; Kim, H. |
| Article Title: | Investigative strategies on lymphatic vessel modulation for treating lymphedema in future medicine |
| Abstract: | Impairment of lymphatic drainage may result in the development of lymphedema, a life-long disorder that results in significant morbidity. However, although lymphedema is common, current treatments are palliative in nature aiming to decrease swelling and control symptoms rather than cure the underlying problem. However, as our understanding in lymphatic biology increases, recent translational studies have described strategies that induce lymphangiogenesis to correct the underlying pathologic problem. These strategies can be classified into three categories: Increase the prolymphangiogenic drive (exogenous vascular endothelial growth factor C [VEGF-C] protein administration or VEGF-C gene delivery); suppress inflammation and inhibit production of antilymphangiogenic molecules (tacrolimus topical administration or leukotriene B4 antagonism); or cell therapy. In this review, we will briefly discuss the mechanisms regulating lymphangiogenesis along with recent translational studies that adopt strategies to modulate these mechanisms. We consider these strategies as candidate therapeutic options that may be in the near future used for the clinical treatment of lymphedema. |
| Keywords: | lymphangiogenesis; lymphedema; lymphatic vessels; tacrolimus; in-vitro; breast-cancer; endothelial growth-factor; gene-therapy; pharmacokinetic; therapeutic; mesenchymal stem-cells; vegf-c; inflammatory lymphangiogenesis; considerations; lymphatic endothelial cells |
| Journal Title: | Precision and Future Medicine |
| Volume: | 2 |
| Issue: | 4 |
| ISSN: | 2508-7940 |
| Publisher: | Sungkyunkwan Univ Sch Medicine |
| Date Published: | 2018-12-01 |
| Start Page: | 149 |
| End Page: | 157 |
| Language: | English |
| ACCESSION: | WOS:000468860600002 |
| DOI: | 10.23838/pfm.2018.00142 |
| PROVIDER: | wos |
| Notes: | Review -- Source: Wos |
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