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Challenging the heterogeneity of disease presentation in malignant melanoma—impact on patient treatment

Marcell Szasz, A. LU ; Malm, Johan LU ; Rezeli, Melinda LU orcid ; Sugihara, Yutaka LU ; Betancourt, Lazaro H. LU ; Rivas, Daniel ; Gyorffy, Balázs and Marko-Varga, György LU (2019) In Cell Biology and Toxicology 35(1). p.1-14
Abstract

There is an increasing global interest to support research areas that can assist in understanding disease and improving patient care. The National Cancer Institute (NIH) has identified precision medicine-based approaches as key research strategies to expedite advances in cancer research. The Cancer Moonshot program (https://www.cancer.gov/research/key-initiatives/moonshot-cancer-initiative) is the largest cancer program of all time, and has been launched to accelerate cancer research that aims to increase the availability of therapies to more patients and, ultimately, to eradicate cancer. Mass spectrometry-based proteomics has been extensively used to study the molecular mechanisms of cancer, to define molecular subtypes of tumors, to... (More)

There is an increasing global interest to support research areas that can assist in understanding disease and improving patient care. The National Cancer Institute (NIH) has identified precision medicine-based approaches as key research strategies to expedite advances in cancer research. The Cancer Moonshot program (https://www.cancer.gov/research/key-initiatives/moonshot-cancer-initiative) is the largest cancer program of all time, and has been launched to accelerate cancer research that aims to increase the availability of therapies to more patients and, ultimately, to eradicate cancer. Mass spectrometry-based proteomics has been extensively used to study the molecular mechanisms of cancer, to define molecular subtypes of tumors, to map cancer-associated protein interaction networks and post-translational modifications, and to aid in the development of new therapeutics and new diagnostic and prognostic tests. To establish the basis for our melanoma studies, we have established the Southern Sweden Malignant Melanoma Biobank. Tissues collected over many years have been accurately characterized with respect to the tumor and patient information. The extreme variability displayed in the protein profiles and the detection of missense mutations has confirmed the complexity and heterogeneity of the disease. It is envisaged that the combined analysis of clinical, histological, and proteomic data will provide patients with a more personalized medical treatment. With respect to disease presentation, targeted treatment and medical mass spectrometry analysis and imaging, this overview report will outline and summarize the current achievements and status within malignant melanoma. We present data generated by our cancer research center in Lund, Sweden, where we have built extensive capabilities in biobanking, proteogenomics, and patient treatments over an extensive time period.

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author
; ; ; ; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Mass spectrometry imaging, Melanoma cancer, Mutation, Proteomics, Tumor heterogeneity
in
Cell Biology and Toxicology
volume
35
issue
1
pages
1 - 14
publisher
Springer
external identifiers
  • pmid:30357519
  • scopus:85055940822
ISSN
0742-2091
DOI
10.1007/s10565-018-9446-9
language
English
LU publication?
yes
id
e57b5b51-529d-4494-9e89-c7327c63f014
date added to LUP
2018-11-20 09:50:34
date last changed
2024-04-15 17:02:00
@article{e57b5b51-529d-4494-9e89-c7327c63f014,
  abstract     = {{<p>There is an increasing global interest to support research areas that can assist in understanding disease and improving patient care. The National Cancer Institute (NIH) has identified precision medicine-based approaches as key research strategies to expedite advances in cancer research. The Cancer Moonshot program (https://www.cancer.gov/research/key-initiatives/moonshot-cancer-initiative) is the largest cancer program of all time, and has been launched to accelerate cancer research that aims to increase the availability of therapies to more patients and, ultimately, to eradicate cancer. Mass spectrometry-based proteomics has been extensively used to study the molecular mechanisms of cancer, to define molecular subtypes of tumors, to map cancer-associated protein interaction networks and post-translational modifications, and to aid in the development of new therapeutics and new diagnostic and prognostic tests. To establish the basis for our melanoma studies, we have established the Southern Sweden Malignant Melanoma Biobank. Tissues collected over many years have been accurately characterized with respect to the tumor and patient information. The extreme variability displayed in the protein profiles and the detection of missense mutations has confirmed the complexity and heterogeneity of the disease. It is envisaged that the combined analysis of clinical, histological, and proteomic data will provide patients with a more personalized medical treatment. With respect to disease presentation, targeted treatment and medical mass spectrometry analysis and imaging, this overview report will outline and summarize the current achievements and status within malignant melanoma. We present data generated by our cancer research center in Lund, Sweden, where we have built extensive capabilities in biobanking, proteogenomics, and patient treatments over an extensive time period.</p>}},
  author       = {{Marcell Szasz, A. and Malm, Johan and Rezeli, Melinda and Sugihara, Yutaka and Betancourt, Lazaro H. and Rivas, Daniel and Gyorffy, Balázs and Marko-Varga, György}},
  issn         = {{0742-2091}},
  keywords     = {{Mass spectrometry imaging; Melanoma cancer; Mutation; Proteomics; Tumor heterogeneity}},
  language     = {{eng}},
  number       = {{1}},
  pages        = {{1--14}},
  publisher    = {{Springer}},
  series       = {{Cell Biology and Toxicology}},
  title        = {{Challenging the heterogeneity of disease presentation in malignant melanoma—impact on patient treatment}},
  url          = {{http://dx.doi.org/10.1007/s10565-018-9446-9}},
  doi          = {{10.1007/s10565-018-9446-9}},
  volume       = {{35}},
  year         = {{2019}},
}