Cell motility and role of ACTC1 in migration of malignant glioma cells
The cytoskeleton, consisting of actin filaments, intermediate filaments, and microtubules, plays an important role in cellmotility during invasion of carcinomas or sarcomas into neighboring tissues. In malignant gliomas, migration of the tumorcells into the brain parenchyma promotes local and/or dis...
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Published in | Progress in Neuro-Oncology Vol. 27; no. 1; pp. 1 - 4 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Kinki Brain Tumor Pathology Conference
31.03.2020
近畿脳腫瘍病理検討会 |
Subjects | |
Online Access | Get full text |
ISSN | 1880-0742 2187-0551 |
DOI | 10.11452/neurooncology.27.1_1 |
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Abstract | The cytoskeleton, consisting of actin filaments, intermediate filaments, and microtubules, plays an important role in cellmotility during invasion of carcinomas or sarcomas into neighboring tissues. In malignant gliomas, migration of the tumorcells into the brain parenchyma promotes local and/or distant metastasis. In this article, the mechanism of cell motility isreviewed, focusing on actin, alpha cardiac muscle 1 (ACTC1) which is one of the six isoforms of actin. Actin is present in two different forms in the cytoplasm, a globular monomer, called G-actin, and a linear polymer, called F-actin or actin filament. Actin filaments form networks through cross linkers. They are important for migration of malignant tumor cells, both through mesenchymal and amoeboid modes. The mesenchymal migration involves polymerization of actin filament at the leading edge of the lamellipodia, and by depolymerization of actin filament at the trailing edge, leading to contraction. On the contrary, the amoeboid migration is induced by the formation of a bleb, formed by contraction of actin-myosin complex in the cytoplasm, close to the cell membrane. The protruded bleb leads to migration through the extracellular matrix.In malignant gliomas, the expression of ACTC1 is upregulated. In clinical situation, patients of ACTC1-positive glioblastoma demonstrated invasion of the contralateral cerebral hemisphere at the time of diagnosis, and distant metastasis in the remote areas of the brain at the time of recurrence. Time-lapse study demonstrated that the in vitro motility of glioblastoma cells was significantly inhibited by knockdown of ACTC1.Actin filament-dependent cell motility is also important in migration of gliomas. Among the various isoforms of actin, ACTC1 may serve as a marker for migration in these malignant cells. |
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AbstractList | The cytoskeleton, consisting of actin filaments, intermediate filaments, and microtubules, plays an important role in cell
motility during invasion of carcinomas or sarcomas into neighboring tissues. In malignant gliomas, migration of the tumor
cells into the brain parenchyma promotes local and/or distant metastasis. In this article, the mechanism of cell motility is
reviewed, focusing on actin, alpha cardiac muscle 1 (ACTC1) which is one of the six isoforms of actin. Actin is present in two different forms in the cytoplasm, a globular monomer, called G-actin, and a linear polymer, called F-actin or actin filament. Actin filaments form networks through cross linkers. They are important for migration of malignant tumor cells, both through mesenchymal and amoeboid modes. The mesenchymal migration involves polymerization of actin filament at the leading edge of the lamellipodia, and by depolymerization of actin filament at the trailing edge, leading to contraction. On the contrary, the amoeboid migration is induced by the formation of a bleb, formed by contraction of actin-myosin complex in the cytoplasm, close to the cell membrane. The protruded bleb leads to migration through the extracellular matrix.In malignant gliomas, the expression of ACTC1 is upregulated. In clinical situation, patients of ACTC1-positive glioblastoma demonstrated invasion of the contralateral cerebral hemisphere at the time of diagnosis, and distant metastasis in the remote areas of the brain at the time of recurrence. Time-lapse study demonstrated that the in vitro motility of glioblastoma cells was significantly inhibited by knockdown of ACTC1.Actin filament-dependent cell motility is also important in migration of gliomas. Among the various isoforms of actin, ACTC1 may serve as a marker for migration in these malignant cells. The cytoskeleton, consisting of actin filaments, intermediate filaments, and microtubules, plays an important role in cellmotility during invasion of carcinomas or sarcomas into neighboring tissues. In malignant gliomas, migration of the tumorcells into the brain parenchyma promotes local and/or distant metastasis. In this article, the mechanism of cell motility isreviewed, focusing on actin, alpha cardiac muscle 1 (ACTC1) which is one of the six isoforms of actin. Actin is present in two different forms in the cytoplasm, a globular monomer, called G-actin, and a linear polymer, called F-actin or actin filament. Actin filaments form networks through cross linkers. They are important for migration of malignant tumor cells, both through mesenchymal and amoeboid modes. The mesenchymal migration involves polymerization of actin filament at the leading edge of the lamellipodia, and by depolymerization of actin filament at the trailing edge, leading to contraction. On the contrary, the amoeboid migration is induced by the formation of a bleb, formed by contraction of actin-myosin complex in the cytoplasm, close to the cell membrane. The protruded bleb leads to migration through the extracellular matrix.In malignant gliomas, the expression of ACTC1 is upregulated. In clinical situation, patients of ACTC1-positive glioblastoma demonstrated invasion of the contralateral cerebral hemisphere at the time of diagnosis, and distant metastasis in the remote areas of the brain at the time of recurrence. Time-lapse study demonstrated that the in vitro motility of glioblastoma cells was significantly inhibited by knockdown of ACTC1.Actin filament-dependent cell motility is also important in migration of gliomas. Among the various isoforms of actin, ACTC1 may serve as a marker for migration in these malignant cells. |
Author | Wanibuchi, Masahiko |
Author_FL | 鰐渕 昌彦 |
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Author_xml | – sequence: 1 fullname: Wanibuchi, Masahiko organization: Department of Neurosurgery Osaka Medical College |
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DocumentTitleAlternate | 悪性神経膠腫の遊走に関与しているACTC1と細胞の運動について |
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References | 5. Parri M, Chiarugi P: Rac and Rho GTPases in cancer cell motility control. Cell Commun Signal 8: 23, 2010 10. Wanibuchi M, Kataoka-Sasaki Y, Sasaki M, Oka S, Otsuka Y, Yamaguchi M, et al: Interleukin-13 receptor alpha 2 as a marker of poorer prognosis in high-grade astrocytomas. J Neurosurg Sci 62: 239- 244, 2018 2. Mogilner A: Mathematics of cell motility: have we got its number? J Math Biol 58: 105-134, 2009 12. Yamazaki D, Kurisu S, Takenawa T: Regulation of cancer cell motility through actin reorganization. Cancer Sci 96: 379-386, 2005 1. Ananthakrishnan R, Ehrlicher A: The forces behind cell movement. Int J Biol Sci 3: 303-317, 2007 9. Small JV, Stradal T, Vignal E, Rottner K: The lamellipodium: where motility begins. Trends Cell Biol 12: 112-120, 2002 4. Ookawa S, Wanibuchi M, Kataoka-Sasaki Y, Sasaki M, Oka S, Ohtaki S, et al: Digital Polymerase Chain Reaction Quantification of SERPINA1 Predicts Prognosis in High-Grade Glioma. World Neurosurg 111: e783-e789, 2018 13. 斉藤康二, 太田安隆: がん細胞の浸潤における運動様式の転換制御. 生化学 89: 90-93, 2017 11. Wanibuchi M, Ohtaki S, Ookawa S, KataokaSasaki Y, Sasaki M, Oka S, et al: Actin, alpha, cardiac muscle 1 (ACTC1) knockdown inhibits the migration of glioblastoma cells in vitro. J Neurol Sci 392: 117-121, 2018 3. Ohtaki S, Wanibuchi M, Kataoka-Sasaki Y, Sasaki M, Oka S, Noshiro S, et al: ACTC1 as an invasion and prognosis marker in glioma. J Neurosurg 126: 467-475, 2017 6. Pollard TD, Borisy GG: Cellular motility driven by assembly and disassembly of actin filaments. Cell 112: 453-465, 2003 7. Sahai E: Mechanisms of cancer cell invasion. Curr Opin Genet Dev 15: 87-96, 2005 8. Sanz-Moreno V, Marshall CJ: The plasticity of cytoskeletal dynamics underlying neoplastic cell migration. Curr Opin Cell Biol 22: 690-696, 2010 |
References_xml | – reference: 9. Small JV, Stradal T, Vignal E, Rottner K: The lamellipodium: where motility begins. Trends Cell Biol 12: 112-120, 2002 – reference: 3. Ohtaki S, Wanibuchi M, Kataoka-Sasaki Y, Sasaki M, Oka S, Noshiro S, et al: ACTC1 as an invasion and prognosis marker in glioma. J Neurosurg 126: 467-475, 2017 – reference: 10. Wanibuchi M, Kataoka-Sasaki Y, Sasaki M, Oka S, Otsuka Y, Yamaguchi M, et al: Interleukin-13 receptor alpha 2 as a marker of poorer prognosis in high-grade astrocytomas. J Neurosurg Sci 62: 239- 244, 2018 – reference: 13. 斉藤康二, 太田安隆: がん細胞の浸潤における運動様式の転換制御. 生化学 89: 90-93, 2017 – reference: 1. Ananthakrishnan R, Ehrlicher A: The forces behind cell movement. Int J Biol Sci 3: 303-317, 2007 – reference: 7. Sahai E: Mechanisms of cancer cell invasion. Curr Opin Genet Dev 15: 87-96, 2005 – reference: 12. Yamazaki D, Kurisu S, Takenawa T: Regulation of cancer cell motility through actin reorganization. Cancer Sci 96: 379-386, 2005 – reference: 11. Wanibuchi M, Ohtaki S, Ookawa S, KataokaSasaki Y, Sasaki M, Oka S, et al: Actin, alpha, cardiac muscle 1 (ACTC1) knockdown inhibits the migration of glioblastoma cells in vitro. J Neurol Sci 392: 117-121, 2018 – reference: 8. Sanz-Moreno V, Marshall CJ: The plasticity of cytoskeletal dynamics underlying neoplastic cell migration. Curr Opin Cell Biol 22: 690-696, 2010 – reference: 2. Mogilner A: Mathematics of cell motility: have we got its number? J Math Biol 58: 105-134, 2009 – reference: 5. Parri M, Chiarugi P: Rac and Rho GTPases in cancer cell motility control. Cell Commun Signal 8: 23, 2010 – reference: 4. Ookawa S, Wanibuchi M, Kataoka-Sasaki Y, Sasaki M, Oka S, Ohtaki S, et al: Digital Polymerase Chain Reaction Quantification of SERPINA1 Predicts Prognosis in High-Grade Glioma. World Neurosurg 111: e783-e789, 2018 – reference: 6. Pollard TD, Borisy GG: Cellular motility driven by assembly and disassembly of actin filaments. Cell 112: 453-465, 2003 |
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Title | Cell motility and role of ACTC1 in migration of malignant glioma cells |
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