The secretory small GTPase Rab27B as a marker for breast cancer progression.
Main Author: | |
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Publication Date: | 2010 |
Other Authors: | , , , , , |
Format: | Article |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | http://hdl.handle.net/10362/145399 |
Summary: | In contemporary oncology practice, an urgent need remains to refine the prognostic assessment of breast cancer. It is still difficult to identify patients with early breast cancer who are likely to benefit from adjuvant chemotherapy. Although invasion of cancer cells is the main prognostic denominator in tumor malignancy, our molecular understanding and diagnosis are often inadequate to cope with this activity. Therefore, deciphering molecular pathways of how tumors invade and metastasize may help in the identification of a useful prognostic marker. We recently discovered that the secretory small GTPase Rab27B, a regulator of vesicle exocytosis, delivers proinvasive signals for increased invasiveness, tumor size, and metastasis of various estrogen receptor (ER)-positive breast cancer cell lines, both in vitro and in vivo. In human breast cancer specimens, the presence of Rab27B protein proved to be associated with a low degree of differentiation and the presence of lymph node metastasis in ER-positive breast cancer. |
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The secretory small GTPase Rab27B as a marker for breast cancer progression.OncologySDG 3 - Good Health and Well-beingIn contemporary oncology practice, an urgent need remains to refine the prognostic assessment of breast cancer. It is still difficult to identify patients with early breast cancer who are likely to benefit from adjuvant chemotherapy. Although invasion of cancer cells is the main prognostic denominator in tumor malignancy, our molecular understanding and diagnosis are often inadequate to cope with this activity. Therefore, deciphering molecular pathways of how tumors invade and metastasize may help in the identification of a useful prognostic marker. We recently discovered that the secretory small GTPase Rab27B, a regulator of vesicle exocytosis, delivers proinvasive signals for increased invasiveness, tumor size, and metastasis of various estrogen receptor (ER)-positive breast cancer cell lines, both in vitro and in vivo. In human breast cancer specimens, the presence of Rab27B protein proved to be associated with a low degree of differentiation and the presence of lymph node metastasis in ER-positive breast cancer.Centro de Estudos de Doenças Crónicas (CEDOC)NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)RUNHendrix, A.Braems, GeertBracke, MarcSeabra, MiguelGahl, WilliamDe Wever, OlivierWestbroek, Wendy2022-11-10T22:13:31Z2010-082010-08-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article5application/pdfhttp://hdl.handle.net/10362/145399eng1949-2553PURE: 47670938https://doi.org/10.18632/oncotarget.140info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-22T18:06:34Zoai:run.unl.pt:10362/145399Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T17:37:07.103612Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
The secretory small GTPase Rab27B as a marker for breast cancer progression. |
title |
The secretory small GTPase Rab27B as a marker for breast cancer progression. |
spellingShingle |
The secretory small GTPase Rab27B as a marker for breast cancer progression. Hendrix, A. Oncology SDG 3 - Good Health and Well-being |
title_short |
The secretory small GTPase Rab27B as a marker for breast cancer progression. |
title_full |
The secretory small GTPase Rab27B as a marker for breast cancer progression. |
title_fullStr |
The secretory small GTPase Rab27B as a marker for breast cancer progression. |
title_full_unstemmed |
The secretory small GTPase Rab27B as a marker for breast cancer progression. |
title_sort |
The secretory small GTPase Rab27B as a marker for breast cancer progression. |
author |
Hendrix, A. |
author_facet |
Hendrix, A. Braems, Geert Bracke, Marc Seabra, Miguel Gahl, William De Wever, Olivier Westbroek, Wendy |
author_role |
author |
author2 |
Braems, Geert Bracke, Marc Seabra, Miguel Gahl, William De Wever, Olivier Westbroek, Wendy |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Centro de Estudos de Doenças Crónicas (CEDOC) NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM) RUN |
dc.contributor.author.fl_str_mv |
Hendrix, A. Braems, Geert Bracke, Marc Seabra, Miguel Gahl, William De Wever, Olivier Westbroek, Wendy |
dc.subject.por.fl_str_mv |
Oncology SDG 3 - Good Health and Well-being |
topic |
Oncology SDG 3 - Good Health and Well-being |
description |
In contemporary oncology practice, an urgent need remains to refine the prognostic assessment of breast cancer. It is still difficult to identify patients with early breast cancer who are likely to benefit from adjuvant chemotherapy. Although invasion of cancer cells is the main prognostic denominator in tumor malignancy, our molecular understanding and diagnosis are often inadequate to cope with this activity. Therefore, deciphering molecular pathways of how tumors invade and metastasize may help in the identification of a useful prognostic marker. We recently discovered that the secretory small GTPase Rab27B, a regulator of vesicle exocytosis, delivers proinvasive signals for increased invasiveness, tumor size, and metastasis of various estrogen receptor (ER)-positive breast cancer cell lines, both in vitro and in vivo. In human breast cancer specimens, the presence of Rab27B protein proved to be associated with a low degree of differentiation and the presence of lymph node metastasis in ER-positive breast cancer. |
publishDate |
2010 |
dc.date.none.fl_str_mv |
2010-08 2010-08-01T00:00:00Z 2022-11-10T22:13:31Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/article |
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article |
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publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10362/145399 |
url |
http://hdl.handle.net/10362/145399 |
dc.language.iso.fl_str_mv |
eng |
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eng |
dc.relation.none.fl_str_mv |
1949-2553 PURE: 47670938 https://doi.org/10.18632/oncotarget.140 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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5 application/pdf |
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