Cargando…

Reduced migration of MLH1 deficient colon cancer cells depends on SPTAN1

INTRODUCTION: Defects in the DNA mismatch repair (MMR) protein MLH1 are frequently observed in sporadic and hereditary colorectal cancers (CRC). Affected tumors generate much less metastatic potential than the MLH1 proficient forms. Although MLH1 has been shown to be not only involved in postreplica...

Descripción completa

Detalles Bibliográficos
Autores principales: Hinrichsen, Inga, Ernst, Benjamin Philipp, Nuber, Franziska, Passmann, Sandra, Schäfer, Dieter, Steinke, Verena, Friedrichs, Nicolaus, Plotz, Guido, Zeuzem, Stefan, Brieger, Angela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3904401/
https://www.ncbi.nlm.nih.gov/pubmed/24456667
http://dx.doi.org/10.1186/1476-4598-13-11
_version_ 1782301207403954176
author Hinrichsen, Inga
Ernst, Benjamin Philipp
Nuber, Franziska
Passmann, Sandra
Schäfer, Dieter
Steinke, Verena
Friedrichs, Nicolaus
Plotz, Guido
Zeuzem, Stefan
Brieger, Angela
author_facet Hinrichsen, Inga
Ernst, Benjamin Philipp
Nuber, Franziska
Passmann, Sandra
Schäfer, Dieter
Steinke, Verena
Friedrichs, Nicolaus
Plotz, Guido
Zeuzem, Stefan
Brieger, Angela
author_sort Hinrichsen, Inga
collection PubMed
description INTRODUCTION: Defects in the DNA mismatch repair (MMR) protein MLH1 are frequently observed in sporadic and hereditary colorectal cancers (CRC). Affected tumors generate much less metastatic potential than the MLH1 proficient forms. Although MLH1 has been shown to be not only involved in postreplicative MMR but also in several MMR independent processes like cytoskeletal organization, the connection between MLH1 and metastasis remains unclear. We recently identified non-erythroid spectrin αII (SPTAN1), a scaffolding protein involved in cell adhesion and motility, to interact with MLH1. In the current study, the interaction of MLH1 and SPTAN1 and its potential consequences for CRC metastasis was evaluated. METHODS: Nine cancer cell lines as well as fresh and paraffin embedded colon cancer tissue from 12 patients were used in gene expression studies of SPTAN1 and MLH1. Co-expression of SPTAN1 and MLH1 was analyzed by siRNA knock down of MLH1 in HeLa, HEK293, MLH1 positive HCT116, SW480 and LoVo cells. Effects on cellular motility were determined in MLH1 deficient HCT116 and MLH1 deficient HEK293T compared to their MLH1 proficient sister cells, respectively. RESULTS: MLH1 deficiency is clearly associated with SPTAN1 reduction. Moreover, siRNA knock down of MLH1 decreased the mRNA level of SPTAN1 in HeLa, HEK293 as well as in MLH1 positive HCT116 cells, which indicates a co-expression of SPTAN1 by MLH1. In addition, cellular motility of MLH1 deficient HCT116 and MLH1 deficient HEK293T cells was impaired compared to the MLH1 proficient sister clones. Consequently, overexpression of SPTAN1 increased migration of MLH1 deficient cells while knock down of SPTAN1 decreased cellular mobility of MLH1 proficient cells, indicating SPTAN1-dependent migration ability. CONCLUSIONS: These data suggest that SPTAN1 levels decreased in concordance with MLH1 reduction and impaired cellular mobility in MLH1 deficient colon cancer cells. Therefore, aggressiveness of MLH1-positive CRC might be related to SPTAN1.
format Online
Article
Text
id pubmed-3904401
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-39044012014-01-29 Reduced migration of MLH1 deficient colon cancer cells depends on SPTAN1 Hinrichsen, Inga Ernst, Benjamin Philipp Nuber, Franziska Passmann, Sandra Schäfer, Dieter Steinke, Verena Friedrichs, Nicolaus Plotz, Guido Zeuzem, Stefan Brieger, Angela Mol Cancer Research INTRODUCTION: Defects in the DNA mismatch repair (MMR) protein MLH1 are frequently observed in sporadic and hereditary colorectal cancers (CRC). Affected tumors generate much less metastatic potential than the MLH1 proficient forms. Although MLH1 has been shown to be not only involved in postreplicative MMR but also in several MMR independent processes like cytoskeletal organization, the connection between MLH1 and metastasis remains unclear. We recently identified non-erythroid spectrin αII (SPTAN1), a scaffolding protein involved in cell adhesion and motility, to interact with MLH1. In the current study, the interaction of MLH1 and SPTAN1 and its potential consequences for CRC metastasis was evaluated. METHODS: Nine cancer cell lines as well as fresh and paraffin embedded colon cancer tissue from 12 patients were used in gene expression studies of SPTAN1 and MLH1. Co-expression of SPTAN1 and MLH1 was analyzed by siRNA knock down of MLH1 in HeLa, HEK293, MLH1 positive HCT116, SW480 and LoVo cells. Effects on cellular motility were determined in MLH1 deficient HCT116 and MLH1 deficient HEK293T compared to their MLH1 proficient sister cells, respectively. RESULTS: MLH1 deficiency is clearly associated with SPTAN1 reduction. Moreover, siRNA knock down of MLH1 decreased the mRNA level of SPTAN1 in HeLa, HEK293 as well as in MLH1 positive HCT116 cells, which indicates a co-expression of SPTAN1 by MLH1. In addition, cellular motility of MLH1 deficient HCT116 and MLH1 deficient HEK293T cells was impaired compared to the MLH1 proficient sister clones. Consequently, overexpression of SPTAN1 increased migration of MLH1 deficient cells while knock down of SPTAN1 decreased cellular mobility of MLH1 proficient cells, indicating SPTAN1-dependent migration ability. CONCLUSIONS: These data suggest that SPTAN1 levels decreased in concordance with MLH1 reduction and impaired cellular mobility in MLH1 deficient colon cancer cells. Therefore, aggressiveness of MLH1-positive CRC might be related to SPTAN1. BioMed Central 2014-01-24 /pmc/articles/PMC3904401/ /pubmed/24456667 http://dx.doi.org/10.1186/1476-4598-13-11 Text en Copyright © 2014 Hinrichsen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Hinrichsen, Inga
Ernst, Benjamin Philipp
Nuber, Franziska
Passmann, Sandra
Schäfer, Dieter
Steinke, Verena
Friedrichs, Nicolaus
Plotz, Guido
Zeuzem, Stefan
Brieger, Angela
Reduced migration of MLH1 deficient colon cancer cells depends on SPTAN1
title Reduced migration of MLH1 deficient colon cancer cells depends on SPTAN1
title_full Reduced migration of MLH1 deficient colon cancer cells depends on SPTAN1
title_fullStr Reduced migration of MLH1 deficient colon cancer cells depends on SPTAN1
title_full_unstemmed Reduced migration of MLH1 deficient colon cancer cells depends on SPTAN1
title_short Reduced migration of MLH1 deficient colon cancer cells depends on SPTAN1
title_sort reduced migration of mlh1 deficient colon cancer cells depends on sptan1
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3904401/
https://www.ncbi.nlm.nih.gov/pubmed/24456667
http://dx.doi.org/10.1186/1476-4598-13-11
work_keys_str_mv AT hinrichseninga reducedmigrationofmlh1deficientcoloncancercellsdependsonsptan1
AT ernstbenjaminphilipp reducedmigrationofmlh1deficientcoloncancercellsdependsonsptan1
AT nuberfranziska reducedmigrationofmlh1deficientcoloncancercellsdependsonsptan1
AT passmannsandra reducedmigrationofmlh1deficientcoloncancercellsdependsonsptan1
AT schaferdieter reducedmigrationofmlh1deficientcoloncancercellsdependsonsptan1
AT steinkeverena reducedmigrationofmlh1deficientcoloncancercellsdependsonsptan1
AT friedrichsnicolaus reducedmigrationofmlh1deficientcoloncancercellsdependsonsptan1
AT plotzguido reducedmigrationofmlh1deficientcoloncancercellsdependsonsptan1
AT zeuzemstefan reducedmigrationofmlh1deficientcoloncancercellsdependsonsptan1
AT briegerangela reducedmigrationofmlh1deficientcoloncancercellsdependsonsptan1