Inflection point in glioma growth and angiogenesis driven by potassium channels
Background and Aim: The overexpression and alternative splicing of calcium-activated potassium channel subunit alpha-1 (KCNMA1) that encodes large-conductance calcium-activated voltage-sensitive potassium (BKCa) channels are implicated in the development of human cancers. Dysfunctional angiogenesis...
| Main Authors: | , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2019-01-01
|
| Series: | Glioma |
| Subjects: | |
| Online Access: | http://www.jglioma.com/article.asp?issn=2589-6113;year=2019;volume=2;issue=2;spage=105;epage=115;aulast=Ningaraj |
| _version_ | 1819207092583530496 |
|---|---|
| author | Nagendra Ningaraj Divya Khaitan |
| author_facet | Nagendra Ningaraj Divya Khaitan |
| author_sort | Nagendra Ningaraj |
| collection | DOAJ |
| description | Background and Aim: The overexpression and alternative splicing of calcium-activated potassium channel subunit alpha-1 (KCNMA1) that encodes large-conductance calcium-activated voltage-sensitive potassium (BKCa) channels are implicated in the development of human cancers. Dysfunctional angiogenesis in hypoxic tumors is a challenge to intravenous anticancer drug treatments. Hypoxic factors also lead to abnormal vascular functions posing hurdle for anticancer drug delivery to tumors. The aim of this study was to explore the role of BKCachannels in tumor angiogenesis, specifically with regard to release of vascular endothelial growth factor (VEGF). Materials and Methods: We subjected the glioma cells under hypoxia and normoxia and studied the expression and activity of BKCachannels in in vitro and in vivo tumor models. Then, we studied the proangiogenic factor, VEGF, in tumors and monitored the neoangiogenic process. The study protocol was approved by the Institutional Animal Care and Use Committee, Mercer University, Atlanta, GA, USA (approved No. A0706007_01) on July 20, 2007. Results: We presented in vivo and cell based in vitro experimental evidence on the direct and indirect interactions of BKCachannels with VEGF signaling. There was evidence that under hypoxia, glioma cells overexpressed KCNMA1 and increased VEGF secretion. By inhibiting KCNMA1, we showed that VEGF secretion was significantly reduced, thus potentially controlling angiogenesis, which has implications for vascular permeability and anticancer drug delivery. Moreover, there were differences in alternate splicing of KCNMA1 between normal and malignant cells under hypoxia and normoxia. Conclusion: We conclude that BKCachannels regulate hypoxia-induced angiogenesis. Therefore, serious effort is needed to better understand the molecular mechanisms of BKCachannelopathies triggering angiogenesis and progression of glioma. The modulators of BKCachannels could be viable in new anticancer therapeutics. |
| first_indexed | 2024-12-23T05:18:00Z |
| format | Article |
| id | doaj.art-d2ac7d3575464fa7a64cbf7d742397f4 |
| institution | Directory Open Access Journal |
| issn | 2589-6113 2589-6121 |
| language | English |
| last_indexed | 2024-12-23T05:18:00Z |
| publishDate | 2019-01-01 |
| publisher | Wolters Kluwer Medknow Publications |
| record_format | Article |
| series | Glioma |
| spelling | doaj.art-d2ac7d3575464fa7a64cbf7d742397f42022-12-21T17:58:47ZengWolters Kluwer Medknow PublicationsGlioma2589-61132589-61212019-01-012210511510.4103/glioma.glioma_12_19Inflection point in glioma growth and angiogenesis driven by potassium channelsNagendra NingarajDivya KhaitanBackground and Aim: The overexpression and alternative splicing of calcium-activated potassium channel subunit alpha-1 (KCNMA1) that encodes large-conductance calcium-activated voltage-sensitive potassium (BKCa) channels are implicated in the development of human cancers. Dysfunctional angiogenesis in hypoxic tumors is a challenge to intravenous anticancer drug treatments. Hypoxic factors also lead to abnormal vascular functions posing hurdle for anticancer drug delivery to tumors. The aim of this study was to explore the role of BKCachannels in tumor angiogenesis, specifically with regard to release of vascular endothelial growth factor (VEGF). Materials and Methods: We subjected the glioma cells under hypoxia and normoxia and studied the expression and activity of BKCachannels in in vitro and in vivo tumor models. Then, we studied the proangiogenic factor, VEGF, in tumors and monitored the neoangiogenic process. The study protocol was approved by the Institutional Animal Care and Use Committee, Mercer University, Atlanta, GA, USA (approved No. A0706007_01) on July 20, 2007. Results: We presented in vivo and cell based in vitro experimental evidence on the direct and indirect interactions of BKCachannels with VEGF signaling. There was evidence that under hypoxia, glioma cells overexpressed KCNMA1 and increased VEGF secretion. By inhibiting KCNMA1, we showed that VEGF secretion was significantly reduced, thus potentially controlling angiogenesis, which has implications for vascular permeability and anticancer drug delivery. Moreover, there were differences in alternate splicing of KCNMA1 between normal and malignant cells under hypoxia and normoxia. Conclusion: We conclude that BKCachannels regulate hypoxia-induced angiogenesis. Therefore, serious effort is needed to better understand the molecular mechanisms of BKCachannelopathies triggering angiogenesis and progression of glioma. The modulators of BKCachannels could be viable in new anticancer therapeutics.http://www.jglioma.com/article.asp?issn=2589-6113;year=2019;volume=2;issue=2;spage=105;epage=115;aulast=NingarajAngiogenesisanthracyclinesgliomaHIF-1hypoxiaMaxi-K/calcium-activated voltage-sensitive potassium channelsvascular endothelial growth factorvascular endothelial growth factor receptor |
| spellingShingle | Nagendra Ningaraj Divya Khaitan Inflection point in glioma growth and angiogenesis driven by potassium channels Glioma Angiogenesis anthracyclines glioma HIF-1 hypoxia Maxi-K/calcium-activated voltage-sensitive potassium channels vascular endothelial growth factor vascular endothelial growth factor receptor |
| title | Inflection point in glioma growth and angiogenesis driven by potassium channels |
| title_full | Inflection point in glioma growth and angiogenesis driven by potassium channels |
| title_fullStr | Inflection point in glioma growth and angiogenesis driven by potassium channels |
| title_full_unstemmed | Inflection point in glioma growth and angiogenesis driven by potassium channels |
| title_short | Inflection point in glioma growth and angiogenesis driven by potassium channels |
| title_sort | inflection point in glioma growth and angiogenesis driven by potassium channels |
| topic | Angiogenesis anthracyclines glioma HIF-1 hypoxia Maxi-K/calcium-activated voltage-sensitive potassium channels vascular endothelial growth factor vascular endothelial growth factor receptor |
| url | http://www.jglioma.com/article.asp?issn=2589-6113;year=2019;volume=2;issue=2;spage=105;epage=115;aulast=Ningaraj |
| work_keys_str_mv | AT nagendraningaraj inflectionpointingliomagrowthandangiogenesisdrivenbypotassiumchannels AT divyakhaitan inflectionpointingliomagrowthandangiogenesisdrivenbypotassiumchannels |