Reactive center loop moiety is essential for the maspin activity on cellular invasion and ubiquitin-proteasome level

Maspin, a tumor suppressor (SERPINB5), inhibits cancer migration, invasion, and metastasis in vitro and in vivo. The tumor-suppressing effects of maspin depend in part on its ability to enhance cell adhesion to extracellular matrix. Although the molecular mechanism of maspin's action is still u...

Full description

Saved in:
Bibliographic Details
Main Authors: Chakkrit Khanaree, Kongthawat Chairatvit, Sittiruk Roytrakul, Ariyaphong Wongnoppavich
Format: Journal
Published: 2018
Subjects:
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84880309087&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/52227
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
id th-cmuir.6653943832-52227
record_format dspace
spelling th-cmuir.6653943832-522272018-09-04T09:33:13Z Reactive center loop moiety is essential for the maspin activity on cellular invasion and ubiquitin-proteasome level Chakkrit Khanaree Kongthawat Chairatvit Sittiruk Roytrakul Ariyaphong Wongnoppavich Biochemistry, Genetics and Molecular Biology Medicine Maspin, a tumor suppressor (SERPINB5), inhibits cancer migration, invasion, and metastasis in vitro and in vivo. The tumor-suppressing effects of maspin depend in part on its ability to enhance cell adhesion to extracellular matrix. Although the molecular mechanism of maspin's action is still unclear, its functional domain is believed to be located at the reactive center loop (RCL). We have elucidated the role of maspin RCL on adhesion, migration, and invasion by transfecting the highly invasive human breast carcinoma MDA-MB-231 cell line with pcDNA3.1-His/FLAG containing wild-type maspin, ovalbumin, or maspin/ovalbumin RCL chimeric mutants in which maspin RCL is replaced by ovalbumin (MOM) and vice versa (OMO). MDA-MB-231 cells transfected with maspin- or OMO-containing recombinant expression plasmid manifested significant increase in adhesion to fibronectin and reduction in in vitro migration and invasion through Matrigel compared with mock transfection or cells transfected with ovalbumin or MOM. Proteomics analysis of maspin- or OMO-transfected MDA-MB-231 cells revealed reduction in contents of proteins known to promote cancer metastasis and those of ubiquitin-proteasome pathway, while those with tumor-suppressing properties were increased. Furthermore, MDA-MB-231 cells containing maspin or OMO transgene have significantly higher levels of ubiquitin and ubiquitinated conjugates, but reduced 20S proteasome chymotrypsin-like activity. These results clearly demonstrate that the tumor-suppressive properties of maspin reside in its RCL domain. Copyright © 2013 Cognizant Comm. Corp. 2018-09-04T09:22:23Z 2018-09-04T09:22:23Z 2013-07-23 Journal 15553906 09650407 2-s2.0-84880309087 10.3727/096504013X13657689383175 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84880309087&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/52227
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Biochemistry, Genetics and Molecular Biology
Medicine
spellingShingle Biochemistry, Genetics and Molecular Biology
Medicine
Chakkrit Khanaree
Kongthawat Chairatvit
Sittiruk Roytrakul
Ariyaphong Wongnoppavich
Reactive center loop moiety is essential for the maspin activity on cellular invasion and ubiquitin-proteasome level
description Maspin, a tumor suppressor (SERPINB5), inhibits cancer migration, invasion, and metastasis in vitro and in vivo. The tumor-suppressing effects of maspin depend in part on its ability to enhance cell adhesion to extracellular matrix. Although the molecular mechanism of maspin's action is still unclear, its functional domain is believed to be located at the reactive center loop (RCL). We have elucidated the role of maspin RCL on adhesion, migration, and invasion by transfecting the highly invasive human breast carcinoma MDA-MB-231 cell line with pcDNA3.1-His/FLAG containing wild-type maspin, ovalbumin, or maspin/ovalbumin RCL chimeric mutants in which maspin RCL is replaced by ovalbumin (MOM) and vice versa (OMO). MDA-MB-231 cells transfected with maspin- or OMO-containing recombinant expression plasmid manifested significant increase in adhesion to fibronectin and reduction in in vitro migration and invasion through Matrigel compared with mock transfection or cells transfected with ovalbumin or MOM. Proteomics analysis of maspin- or OMO-transfected MDA-MB-231 cells revealed reduction in contents of proteins known to promote cancer metastasis and those of ubiquitin-proteasome pathway, while those with tumor-suppressing properties were increased. Furthermore, MDA-MB-231 cells containing maspin or OMO transgene have significantly higher levels of ubiquitin and ubiquitinated conjugates, but reduced 20S proteasome chymotrypsin-like activity. These results clearly demonstrate that the tumor-suppressive properties of maspin reside in its RCL domain. Copyright © 2013 Cognizant Comm. Corp.
format Journal
author Chakkrit Khanaree
Kongthawat Chairatvit
Sittiruk Roytrakul
Ariyaphong Wongnoppavich
author_facet Chakkrit Khanaree
Kongthawat Chairatvit
Sittiruk Roytrakul
Ariyaphong Wongnoppavich
author_sort Chakkrit Khanaree
title Reactive center loop moiety is essential for the maspin activity on cellular invasion and ubiquitin-proteasome level
title_short Reactive center loop moiety is essential for the maspin activity on cellular invasion and ubiquitin-proteasome level
title_full Reactive center loop moiety is essential for the maspin activity on cellular invasion and ubiquitin-proteasome level
title_fullStr Reactive center loop moiety is essential for the maspin activity on cellular invasion and ubiquitin-proteasome level
title_full_unstemmed Reactive center loop moiety is essential for the maspin activity on cellular invasion and ubiquitin-proteasome level
title_sort reactive center loop moiety is essential for the maspin activity on cellular invasion and ubiquitin-proteasome level
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84880309087&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/52227
_version_ 1681423912574910464