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Angiogenesis and vasculogenic mimicry as therapeutic targets in ovarian cancer

Authors
Lim, DansaemDo, YeojinKwon, Byung SuChang, WoochulLee, Myeong-SokKim, JongminCho, Jin Gu
Issue Date
Jun-2020
Publisher
KOREAN SOCIETY BIOCHEMISTRY & MOLECULAR BIOLOGY
Keywords
Angiogenesis; Ovarian cancer; Therapeutic target; Tumor vascularization; Vasculogenic mimicry
Citation
BMB REPORTS, v.53, no.6, pp 291 - 298
Pages
8
Journal Title
BMB REPORTS
Volume
53
Number
6
Start Page
291
End Page
298
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/1472
DOI
10.5483/BMBRep.2020.53.6.060
ISSN
1976-6696
1976-670X
Abstract
Tumor angiogenesis is an essential process for growth and metastasis of cancer cells as it supplies tumors with oxygen and nutrients. During tumor angiogenesis, many pro-angiogenic factors are secreted by tumor cells to induce their own vascularization via activation of pre-existing host endothelium. However, accumulating evidence suggests that vasculogenic mimicry (VM) is a key alternative mechanism for tumor vascularization when tumors are faced with insufficient supply of oxygen and nutrients. VM is a tumor vascularization mechanism in which tumors create a blood supply system, in contrast to tumor angiogenesis mechanisms that depend on pre-existing host endothelium. VM is closely associated with tumor progression and poor prognosis in many cancels. Therefore, inhibition of VM may be a promising therapeutic strategy and may overcome the limitations of anti-angiogenesis therapy for cancer patients. In this review, we provide an overview of the current anti-angiogenic therapies for ovarian cancer and the current state of knowledge regarding the links between microRNAs and the VM process, with a focus on the mechanism that regulates associated signaling pathways in ovarian cancer. Moreover, we discuss the potential for VM as a therapeutic strategy against ovarian cancer.
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