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Establishing a Southern Swedish Malignant Melanoma OMICS and biobank clinical capability

BACKGROUND: The objectives and goals of the Southern Swedish Malignant Melanoma (SSMM) are to develop, build and utilize cutting edge biobanks and OMICS platforms to better understand disease pathology and drug mechanisms. The SSMM research team is a truly cross-functional group with members from on...

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Autores principales: Welinder, Charlotte, Jönsson, Göran, Ingvar, Christian, Lundgren, Lotta, Olsson, Håkan, Breslin, Thomas, Végvári, Ákos, Laurell, Thomas, Rezeli, Melinda, Jansson, Bo, Baldetorp, Bo, Marko-Varga, György
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3599425/
https://www.ncbi.nlm.nih.gov/pubmed/23445834
http://dx.doi.org/10.1186/2001-1326-2-7
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author Welinder, Charlotte
Jönsson, Göran
Ingvar, Christian
Lundgren, Lotta
Olsson, Håkan
Breslin, Thomas
Végvári, Ákos
Laurell, Thomas
Rezeli, Melinda
Jansson, Bo
Baldetorp, Bo
Marko-Varga, György
author_facet Welinder, Charlotte
Jönsson, Göran
Ingvar, Christian
Lundgren, Lotta
Olsson, Håkan
Breslin, Thomas
Végvári, Ákos
Laurell, Thomas
Rezeli, Melinda
Jansson, Bo
Baldetorp, Bo
Marko-Varga, György
author_sort Welinder, Charlotte
collection PubMed
description BACKGROUND: The objectives and goals of the Southern Swedish Malignant Melanoma (SSMM) are to develop, build and utilize cutting edge biobanks and OMICS platforms to better understand disease pathology and drug mechanisms. The SSMM research team is a truly cross-functional group with members from oncology, surgery, bioinformatics, proteomics, and genomics initiatives. Within the research team there are members who daily diagnose patients with suspect melanomas, do follow-ups on malignant melanoma patients and remove primary or metastatic lesions by surgery. This inter-disciplinary clinical patient care ensures a competence build as well as a best practice procedure where the patient benefits. METHODS: Clinical materials from patients before, during and after treatments with clinical end points are being collected. Tissue samples as well as bio-fluid samples such as blood fractions, plasma, serum and whole blood will be archived in 384-high density sample tube formats. Standardized approaches for patient selections, patient sampling, sample-processing and analysis platforms with dedicated protein assays and genomics platforms that will hold value for the research community are used. The patient biobank archives are fully automated with novel ultralow temperature biobank storage units and used as clinical resources. RESULTS: An IT-infrastructure using a laboratory information management system (LIMS) has been established, that is the key interface for the research teams in order to share and explore data generated within the project. The cross-site data repository in Lund forms the basis for sample processing, together with biological samples in southern Sweden, including blood fractions and tumor tissues. Clinical registries are associated with the biobank materials, including pathology reports on disease diagnosis on the malignant melanoma (MM) patients. CONCLUSIONS: We provide data on the developments of protein profiling and targeted protein assays on isolated melanoma tumors, as well as reference blood standards that is used by the team members in the respective laboratories. These pilot data show biobank access and feasibility of performing quantitative proteomics in MM biobank repositories collected in southern Sweden. The scientific outcomes further strengthen the build of healthcare benefit in the complex challenges of malignant melanoma pathophysiology that is addressed by the novel personalized medicines entering the market.
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spelling pubmed-35994252013-03-19 Establishing a Southern Swedish Malignant Melanoma OMICS and biobank clinical capability Welinder, Charlotte Jönsson, Göran Ingvar, Christian Lundgren, Lotta Olsson, Håkan Breslin, Thomas Végvári, Ákos Laurell, Thomas Rezeli, Melinda Jansson, Bo Baldetorp, Bo Marko-Varga, György Clin Transl Med Research BACKGROUND: The objectives and goals of the Southern Swedish Malignant Melanoma (SSMM) are to develop, build and utilize cutting edge biobanks and OMICS platforms to better understand disease pathology and drug mechanisms. The SSMM research team is a truly cross-functional group with members from oncology, surgery, bioinformatics, proteomics, and genomics initiatives. Within the research team there are members who daily diagnose patients with suspect melanomas, do follow-ups on malignant melanoma patients and remove primary or metastatic lesions by surgery. This inter-disciplinary clinical patient care ensures a competence build as well as a best practice procedure where the patient benefits. METHODS: Clinical materials from patients before, during and after treatments with clinical end points are being collected. Tissue samples as well as bio-fluid samples such as blood fractions, plasma, serum and whole blood will be archived in 384-high density sample tube formats. Standardized approaches for patient selections, patient sampling, sample-processing and analysis platforms with dedicated protein assays and genomics platforms that will hold value for the research community are used. The patient biobank archives are fully automated with novel ultralow temperature biobank storage units and used as clinical resources. RESULTS: An IT-infrastructure using a laboratory information management system (LIMS) has been established, that is the key interface for the research teams in order to share and explore data generated within the project. The cross-site data repository in Lund forms the basis for sample processing, together with biological samples in southern Sweden, including blood fractions and tumor tissues. Clinical registries are associated with the biobank materials, including pathology reports on disease diagnosis on the malignant melanoma (MM) patients. CONCLUSIONS: We provide data on the developments of protein profiling and targeted protein assays on isolated melanoma tumors, as well as reference blood standards that is used by the team members in the respective laboratories. These pilot data show biobank access and feasibility of performing quantitative proteomics in MM biobank repositories collected in southern Sweden. The scientific outcomes further strengthen the build of healthcare benefit in the complex challenges of malignant melanoma pathophysiology that is addressed by the novel personalized medicines entering the market. Springer 2013-02-27 /pmc/articles/PMC3599425/ /pubmed/23445834 http://dx.doi.org/10.1186/2001-1326-2-7 Text en Copyright ©2013 Welinder et al; licensee Springer. 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
Welinder, Charlotte
Jönsson, Göran
Ingvar, Christian
Lundgren, Lotta
Olsson, Håkan
Breslin, Thomas
Végvári, Ákos
Laurell, Thomas
Rezeli, Melinda
Jansson, Bo
Baldetorp, Bo
Marko-Varga, György
Establishing a Southern Swedish Malignant Melanoma OMICS and biobank clinical capability
title Establishing a Southern Swedish Malignant Melanoma OMICS and biobank clinical capability
title_full Establishing a Southern Swedish Malignant Melanoma OMICS and biobank clinical capability
title_fullStr Establishing a Southern Swedish Malignant Melanoma OMICS and biobank clinical capability
title_full_unstemmed Establishing a Southern Swedish Malignant Melanoma OMICS and biobank clinical capability
title_short Establishing a Southern Swedish Malignant Melanoma OMICS and biobank clinical capability
title_sort establishing a southern swedish malignant melanoma omics and biobank clinical capability
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3599425/
https://www.ncbi.nlm.nih.gov/pubmed/23445834
http://dx.doi.org/10.1186/2001-1326-2-7
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