| Literature DB >> 30168025 |
Shuo Li1,2,3,4, Hua-Xiang Xu1,2,3,4, Chun-Tao Wu1,2,3,4, Wen-Quan Wang1,2,3,4, Wei Jin1,2,3,4, He-Li Gao1,2,3,4, Hao Li1,2,3,4, Shi-Rong Zhang1,2,3,4, Jin-Zhi Xu1,2,3,4, Zi-Hao Qi1,2,3,4, Quan-Xing Ni1,2,3,4, Xian-Jun Yu5,6,7,8, Liang Liu9,10,11,12.
Abstract
Pancreatic cancer is one of the most lethal malignancies worldwide. Although the standard of care in pancreatic cancer has improved, prognoses for patients remain poor with a 5-year survival rate of < 5%. Angiogenesis, namely, the formation of new blood vessels from pre-existing vessels, is an important event in tumor growth and hematogenous metastasis. It is a dynamic and complex process involving multiple mechanisms and is regulated by various molecules. Inhibition of angiogenesis has been an established therapeutic strategy for many solid tumors. However, clinical outcomes are far from satisfying for pancreatic cancer patients receiving anti-angiogenic therapies. In this review, we summarize the current status of angiogenesis in pancreatic cancer research and explore the reasons for the poor efficacy of anti-angiogenic therapies, aiming to identify some potential therapeutic targets that may enhance the effectiveness of anti-angiogenic treatments.Entities:
Keywords: Angiogenesis; Anti-angiogenic therapy; Microvessel density; Pancreatic cancer; Stromal components
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Year: 2018 PMID: 30168025 DOI: 10.1007/s10456-018-9645-2
Source DB: PubMed Journal: Angiogenesis ISSN: 0969-6970 Impact factor: 9.596