2014
DOI: 10.1134/s1068162014060144
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Key enzymes of degradation and angiogenesis as factors of tumor progression for squamous-cell cervical carcinoma

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Cited by 6 publications
(7 citation statements)
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“…Moreover, there is a close relationship between MET and MMPs [ 42 ]. In addition, it has been demonstrated that MMPs upregulate VEGF expression in endotheliocytes and tumor cells and promote interaction of VEGF and its receptors, inducing angiogenesis [ 43 ]. Therefore, there is a close relationship between MET, angiogenesis, and MMPs.…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, there is a close relationship between MET and MMPs [ 42 ]. In addition, it has been demonstrated that MMPs upregulate VEGF expression in endotheliocytes and tumor cells and promote interaction of VEGF and its receptors, inducing angiogenesis [ 43 ]. Therefore, there is a close relationship between MET, angiogenesis, and MMPs.…”
Section: Discussionmentioning
confidence: 99%
“…MMP-2 and MMP-9 may be involved in the regulation of angiogenesis in tumor invasion and metastasis and may promote the release and migration of vascular endothelial cells from basement membrane (BM) by degradation of BM and ECM. MMP-2 can upregulate angiogenic cytokines through the following processes: (1) degradation of collagen IV, which exposes the binding sites of integrin α V β 3 and promotes the migration of endothelial cells [108]; (2) promoting the synthesis of VEGF and activating the inactive TGF- β ; (3) degradation of matrix components, release of basic FGF and VEGF combined with matrix components [109]; and (4) release of membrane-bound TNF- α and other cytokines that promote angiogenesis by the degradation of vascular BM. MMPs may also have adverse effects on tumor angiogenesis.…”
Section: Extracellular Proteinsmentioning
confidence: 99%
“…Table 3 shows most tumor cell lines (thyroid carcinoma cells ML-1 and ONCO-DG1, gastric carcinoma cells SGC-7901, U251 glioma cells, MDA-MB-231 breast cancer cells and BL6-10 melanoma cells) under SMG present the phenomenon of increased apoptosis [25, 36, 41, 44, 45, 47], but decreased apoptosis in MIP-101 poorly differentiated colorectal carcinoma ceils [19] and absence of obvious apoptosis in squamous cell carcinoma of the cervix (SCC) and ML-1 thyroid cancer are also observed [26, 109]. Cell cycle arrest, abnormal expression of apoptosis-related proteins (increased P21, P53, Fas and Bax; decreased the Bcl-2), tumor suppressor genes ( PTEN and P53 up-regulation) is often found in cancer cell lines [20, 25, 36, 41, 43, 45] (MDA-MB-231 and MCF-7 breast cancer cells, ML-1 and ONCO-DG1 thyroid carcinoma cells, DLD-1 colorectal cancer cells and U251 glioma cells) with increased apoptosis.…”
Section: Apoptosismentioning
confidence: 99%
“…2 А1, А2). Эти данные согласуются с результатами более раннего исследования, в котором мы показали, что при ПКШМ наблюдается увеличение экспрессии ММП-9 в большинстве опухолей, а уровень экспрессии отражает метастатический и инвазивный потенциал опухоли [28]. Гиперэкспрессия ММП-9 в опухолях при ПКШМ была продемонстрирована также в ряде других исследований в тканях карцином шейки матки и образцах опухолей, находящихся на разных стадиях дифференцировки [29].…”
Section: Discussionunclassified