2018
DOI: 10.1016/j.biopha.2018.05.134
|View full text |Cite
|
Sign up to set email alerts
|

Survivin is critically involved in VEGFR2 signaling-mediated esophageal cancer cell survival

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
7
0

Year Published

2019
2019
2024
2024

Publication Types

Select...
8
1

Relationship

0
9

Authors

Journals

citations
Cited by 11 publications
(7 citation statements)
references
References 29 publications
0
7
0
Order By: Relevance
“…Also, in vivo studies have shown that Survivin was minimally expressed in the endothelium of normal skin, but was significantly upregulated during angiogenesis in newly formed blood vessels in granulation tissue (O'Connor, Schechner, et al, 2000). Meng et al demonstrated that VEGFR signaling upregulated Survivin expression via the AKT/MDM2 pathway and that this was essential for tumor cell survival (Meng, et al, 2018). It has also been shown in glioma cells that Survivin can promote endothelial cell migration and proliferation and also increase microvessel density (a surrogate marker for tumor angiogenesis); moreover, this was attributed to Survivin-induced expression of angiogenic factors VEGF and FGF (P. .…”
Section: Angiogenesismentioning
confidence: 99%
“…Also, in vivo studies have shown that Survivin was minimally expressed in the endothelium of normal skin, but was significantly upregulated during angiogenesis in newly formed blood vessels in granulation tissue (O'Connor, Schechner, et al, 2000). Meng et al demonstrated that VEGFR signaling upregulated Survivin expression via the AKT/MDM2 pathway and that this was essential for tumor cell survival (Meng, et al, 2018). It has also been shown in glioma cells that Survivin can promote endothelial cell migration and proliferation and also increase microvessel density (a surrogate marker for tumor angiogenesis); moreover, this was attributed to Survivin-induced expression of angiogenic factors VEGF and FGF (P. .…”
Section: Angiogenesismentioning
confidence: 99%
“…In vitro experiments also revealed that some tumor cell lines may express VEGF and VEGFR, allowing VEGF to function as both an autocrine and paracrine factor, which results in a positive feedback loop that directly affects tumor cells [243]. The induction of anti-apoptotic proteins Bcl-2 and survivin, both of which are introduced by VEGF, also play a crucial role in tumor progression by protecting the neovasculature of tumors from apoptosis [244]. Additionally, VEGF promotes the release and activation of extracellular matrix-degrading enzymes such as plasminogen activator and the MMP interstitial collagenase, enabling the unrestricted growth of newly formed blood vessels [245].…”
Section: Vegf Biology In Cancermentioning
confidence: 99%
“…In addition to this, it also transmits its apoptotic effects through the cleavage of Caspase-3 and PARP in OC cells [ 102 ]. And Survivin blocks apoptosis by inhibiting Caspase-3 and Caspase-7 [ 103 ].…”
Section: Pathogenesis Of Ocmentioning
confidence: 99%