ADAMTS4 is upregulated in colorectal cancer and could be a useful prognostic indicator of colorectal cancer
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Revista da Associação Médica Brasileira (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302020000100042 |
Resumo: | SUMMARY OBJECTIVE ADAMTS4 is a member of the ADAMTS4 family, which secretes proteinases. The mechanism of tumor metastasis may be correlated to its promotion of angiogenesis. It was determined whether ADAMTS4 participates in colorectal cancer progression. Methods The expression in clinical samples and CRC cell lines was investigated. Using immunohistochemistry (IHC), fluorescence in situ hybridization (FISH), and RT-PCR, the expression of ADAMTS4 was determined in colorectal tumors of different cancer stages and anatomic sites, and in three cell lines of different aggressiveness. Results The overexpression of ADAMTS4 was observed in tissue samples by IHC, and this was mainly located in the cytoplasm, as detected by FISH. The qRT-PCR and western blot analyses further supported the clinical sample findings. Conclusion The present data support the notion that the overexpression of ADAMTS4 in CRC might be useful as a non-invasive biomarker for detecting CRC in patients. |
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Revista da Associação Médica Brasileira (Online) |
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ADAMTS4 is upregulated in colorectal cancer and could be a useful prognostic indicator of colorectal cancerNeoplasmsNeoplasm MetastasisADAMTS4 ProteinSUMMARY OBJECTIVE ADAMTS4 is a member of the ADAMTS4 family, which secretes proteinases. The mechanism of tumor metastasis may be correlated to its promotion of angiogenesis. It was determined whether ADAMTS4 participates in colorectal cancer progression. Methods The expression in clinical samples and CRC cell lines was investigated. Using immunohistochemistry (IHC), fluorescence in situ hybridization (FISH), and RT-PCR, the expression of ADAMTS4 was determined in colorectal tumors of different cancer stages and anatomic sites, and in three cell lines of different aggressiveness. Results The overexpression of ADAMTS4 was observed in tissue samples by IHC, and this was mainly located in the cytoplasm, as detected by FISH. The qRT-PCR and western blot analyses further supported the clinical sample findings. Conclusion The present data support the notion that the overexpression of ADAMTS4 in CRC might be useful as a non-invasive biomarker for detecting CRC in patients.Associação Médica Brasileira2020-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302020000100042Revista da Associação Médica Brasileira v.66 n.1 2020reponame:Revista da Associação Médica Brasileira (Online)instname:Associação Médica Brasileira (AMB)instacron:AMB10.1590/1806-9282.66.1.42info:eu-repo/semantics/openAccessShang,Xue-QinLiu,Kui-LiangLi,QianLao,Yue-QiongLi,Nan-ShanWu,Jingeng2020-02-19T00:00:00Zoai:scielo:S0104-42302020000100042Revistahttps://ramb.amb.org.br/ultimas-edicoes/#https://old.scielo.br/oai/scielo-oai.php||ramb@amb.org.br1806-92820104-4230opendoar:2020-02-19T00:00Revista da Associação Médica Brasileira (Online) - Associação Médica Brasileira (AMB)false |
dc.title.none.fl_str_mv |
ADAMTS4 is upregulated in colorectal cancer and could be a useful prognostic indicator of colorectal cancer |
title |
ADAMTS4 is upregulated in colorectal cancer and could be a useful prognostic indicator of colorectal cancer |
spellingShingle |
ADAMTS4 is upregulated in colorectal cancer and could be a useful prognostic indicator of colorectal cancer Shang,Xue-Qin Neoplasms Neoplasm Metastasis ADAMTS4 Protein |
title_short |
ADAMTS4 is upregulated in colorectal cancer and could be a useful prognostic indicator of colorectal cancer |
title_full |
ADAMTS4 is upregulated in colorectal cancer and could be a useful prognostic indicator of colorectal cancer |
title_fullStr |
ADAMTS4 is upregulated in colorectal cancer and could be a useful prognostic indicator of colorectal cancer |
title_full_unstemmed |
ADAMTS4 is upregulated in colorectal cancer and could be a useful prognostic indicator of colorectal cancer |
title_sort |
ADAMTS4 is upregulated in colorectal cancer and could be a useful prognostic indicator of colorectal cancer |
author |
Shang,Xue-Qin |
author_facet |
Shang,Xue-Qin Liu,Kui-Liang Li,Qian Lao,Yue-Qiong Li,Nan-Shan Wu,Jing |
author_role |
author |
author2 |
Liu,Kui-Liang Li,Qian Lao,Yue-Qiong Li,Nan-Shan Wu,Jing |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Shang,Xue-Qin Liu,Kui-Liang Li,Qian Lao,Yue-Qiong Li,Nan-Shan Wu,Jing |
dc.subject.por.fl_str_mv |
Neoplasms Neoplasm Metastasis ADAMTS4 Protein |
topic |
Neoplasms Neoplasm Metastasis ADAMTS4 Protein |
description |
SUMMARY OBJECTIVE ADAMTS4 is a member of the ADAMTS4 family, which secretes proteinases. The mechanism of tumor metastasis may be correlated to its promotion of angiogenesis. It was determined whether ADAMTS4 participates in colorectal cancer progression. Methods The expression in clinical samples and CRC cell lines was investigated. Using immunohistochemistry (IHC), fluorescence in situ hybridization (FISH), and RT-PCR, the expression of ADAMTS4 was determined in colorectal tumors of different cancer stages and anatomic sites, and in three cell lines of different aggressiveness. Results The overexpression of ADAMTS4 was observed in tissue samples by IHC, and this was mainly located in the cytoplasm, as detected by FISH. The qRT-PCR and western blot analyses further supported the clinical sample findings. Conclusion The present data support the notion that the overexpression of ADAMTS4 in CRC might be useful as a non-invasive biomarker for detecting CRC in patients. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-01-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302020000100042 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302020000100042 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/1806-9282.66.1.42 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Associação Médica Brasileira |
publisher.none.fl_str_mv |
Associação Médica Brasileira |
dc.source.none.fl_str_mv |
Revista da Associação Médica Brasileira v.66 n.1 2020 reponame:Revista da Associação Médica Brasileira (Online) instname:Associação Médica Brasileira (AMB) instacron:AMB |
instname_str |
Associação Médica Brasileira (AMB) |
instacron_str |
AMB |
institution |
AMB |
reponame_str |
Revista da Associação Médica Brasileira (Online) |
collection |
Revista da Associação Médica Brasileira (Online) |
repository.name.fl_str_mv |
Revista da Associação Médica Brasileira (Online) - Associação Médica Brasileira (AMB) |
repository.mail.fl_str_mv |
||ramb@amb.org.br |
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1754212834715107328 |