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...

Full description

Saved in:
Bibliographic Details
Published inProgress in Neuro-Oncology Vol. 27; no. 1; pp. 1 - 4
Main Author Wanibuchi, Masahiko
Format Journal Article
LanguageEnglish
Published Kinki Brain Tumor Pathology Conference 31.03.2020
近畿脳腫瘍病理検討会
Subjects
Online AccessGet full text
ISSN1880-0742
2187-0551
DOI10.11452/neurooncology.27.1_1

Cover

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.
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
Author_FL_xml – sequence: 1
  fullname: 鰐渕 昌彦
Author_xml – sequence: 1
  fullname: Wanibuchi, Masahiko
  organization: Department of Neurosurgery Osaka Medical College
BackLink https://cir.nii.ac.jp/crid/1390283659867746176$$DView record in CiNii
BookMark eNpVkDFPwzAUhC0EEqX0JyB5YE3xsx3bGauoBaRKLN0tN3kOrhwbJWHovydVYWC5k-473XAP5DblhIQ8AVsDyJK_JPweck5Njrk7r7leg4UbsuBgdMHKEm7JAoxhBdOS35PVOJ4YY8CNklwvyK7GGGmfpxDDdKYutXTIEWn2dFMfaqAh0T50g5tCTpe0dzF0yaWJdjHk3tFmHhgfyZ13ccTVry_JYbc91G_F_uP1vd7si1MFqigFZyi95i1WXszuStVw3hp9PBpZzUR4lOgaj0oo2aLmR8lAIlPe65KJJXm-zqYQbBMuCqJi3AhVVkZpLRVoNde219ppnFyH9msIvRvO1g1TaCLaf5dZri1c5Y83n26wmMQPQjRq-g
ContentType Journal Article
Copyright 2020 Kinki Brain Tumor Pathology Conference
Copyright_xml – notice: 2020 Kinki Brain Tumor Pathology Conference
DBID RYH
DOI 10.11452/neurooncology.27.1_1
DatabaseName CiNii Complete
DatabaseTitleList

DeliveryMethod fulltext_linktorsrc
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
DocumentTitle_FL 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
EISSN 2187-0551
EndPage 4
ExternalDocumentID 130007825989
article_neurooncology_27_1_27_1_article_char_en
GroupedDBID ALMA_UNASSIGNED_HOLDINGS
JSF
JSH
KQ8
RJT
RZJ
RYH
ID FETCH-LOGICAL-j916-5320e4f72de9f3f72a56c22d87bb8494f73fe4eacfe6364de72b4014e06ff7503
ISSN 1880-0742
IngestDate Thu Jun 26 22:20:15 EDT 2025
Wed Apr 05 05:10:46 EDT 2023
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed false
IsScholarly false
Issue 1
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-j916-5320e4f72de9f3f72a56c22d87bb8494f73fe4eacfe6364de72b4014e06ff7503
OpenAccessLink https://www.jstage.jst.go.jp/article/neurooncology/27/1/27_1/_article/-char/en
PageCount 4
ParticipantIDs nii_cinii_1390283659867746176
jstage_primary_article_neurooncology_27_1_27_1_article_char_en
PublicationCentury 2000
PublicationDate 2020/03/31
2020-03-31
PublicationDateYYYYMMDD 2020-03-31
PublicationDate_xml – month: 03
  year: 2020
  text: 2020/03/31
  day: 31
PublicationDecade 2020
PublicationTitle Progress in Neuro-Oncology
PublicationTitleAlternate Prog Neuro Oncol
PublicationTitle_FL Neuro-Oncologyの進歩
Prog Neuro Oncol
PublicationYear 2020
Publisher Kinki Brain Tumor Pathology Conference
近畿脳腫瘍病理検討会
Publisher_xml – name: Kinki Brain Tumor Pathology Conference
– name: 近畿脳腫瘍病理検討会
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
SSID ssj0001286427
Score 1.719816
Snippet The cytoskeleton, consisting of actin filaments, intermediate filaments, and microtubules, plays an important role in cellmotility during invasion of...
The cytoskeleton, consisting of actin filaments, intermediate filaments, and microtubules, plays an important role in cell motility during invasion of...
SourceID nii
jstage
SourceType Publisher
StartPage 1
SubjectTerms ACTC1
actin
cell motility
cytoskeleton
glioma
migration
Title Cell motility and role of ACTC1 in migration of malignant glioma cells
URI https://www.jstage.jst.go.jp/article/neurooncology/27/1/27_1/_article/-char/en
https://cir.nii.ac.jp/crid/1390283659867746176
Volume 27
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
ispartofPNX Progress in Neuro-Oncology, 2020/03/31, Vol.27(1), pp.1-4
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3NT9swFLcKXHaZNsE0xph84Fa5y4edOJdpqBpCQwyQMolbFCd2CVsTVMplf_3es900oEqDXZzKTpM4P8f-vef3QcgRjCJpSqNYFZcgoGRKsMwIwRSQkUhqKXSFguL5j-T0J_9-La5Ho69D75KlmlR_NvqV_A-qUAe4opfsC5DtLwoV8BvwhRIQhvJZGE9R8YbWdJZLW0txbyx4PM2nIeoy5s1s0bPCOZDuGVq-jGe_m25ejlFtfz_kp5doroWTH_zVxu1gF231RPPeNgozqIzPy_vypvnVDRUHICV6TzoP9RnmZoARVMIF84d5t8CkADcu8NPa23AwNcKXzlCSdiuHrQN-kLJA-JCxfj51vv6Pxo2bHMPBKss3T99c2Hiw2L_Od28SpZOwCNfrVW9FiDtxyHBEJrMtshOlqd2oP7uSAy2bBAHLZthZPb5348Jbfd50I6Ait0DMMeLCVts0A7aRvyGvvZhAjx3mb8lIt7vkBPGmK7wp4E0Rb9oZavGmTUt7vLG2x5s6vKnFe4_kJ9_y6SnzeTDYLZB3hqk7NDdpVOvMxHAsRVJFUS1TpSTPoCU2msMCanQSJ7zWaaRAauY6SIzBbep3ZLvtWv2eUCu9cpPUFZwiMyN5hQRRh7EJgjqI98kX1_fizsU6KfzYLh69qSJKi9AVq3b0EYRPcp8cwjsrqgZLEC6QvSaYAgCkDODKyYd_tB-QV-uh-pFsLxcP-hBY31J9ssD-BYhDWPE
linkProvider Colorado Alliance of Research Libraries
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Cell+motility+and+role+of+ACTC1+in+migration+of+malignant+glioma+cells&rft.jtitle=Progress+in+Neuro-Oncology&rft.au=Wanibuchi+Masahiko&rft.date=2020-03-31&rft.pub=Kinki+Brain+Tumor+Pathology+Conference&rft.issn=1880-0742&rft.eissn=2187-0551&rft.volume=27&rft.issue=1&rft.spage=1&rft.epage=4&rft_id=info:doi/10.11452%2Fneurooncology.27.1_1&rft.externalDocID=130007825989
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1880-0742&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1880-0742&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1880-0742&client=summon