Literature DB >> 15290709

The potentials of MS-based subproteomic approaches in medical science: the case of lysosomes and breast cancer.

Agnès Journet1, Myriam Ferro.   

Abstract

Because of the great number of women who are diagnosed with breast cancer each year, and though this disease presents the lowest mortality rate among cancers, breast cancer remains a major public health problem. As for any cancer, the tumorigenic and metastatic processes are still hardly understood, and the biochemical markers that allow either a precise monitoring of the disease or the classification of the numerous forms of breast cancer remain too scarce. Therefore, great hopes are put on the development of high-throughput genomic and proteomic technologies. Such comprehensive techniques should help in understanding the processes and in defining steps of the disease by depicting specific genes or protein profiles. Because techniques dedicated to the current proteomic challenges are continuously improving, the probability of the discovery of new potential protein biomarkers is rapidly increasing. In addition, the identification of such markers should be eased by lowering the sample complexity; e.g., by sample fractionation, either according to specific physico-chemical properties of the proteins, or by focusing on definite subcellular compartments. In particular, proteins of the lysosomal compartment have been shown to be prone to alterations in their localization, expression, or post-translational modifications (PTMs) during the cancer process. Some of them, such as the aspartic protease cathepsin D (CatD), have even been proven as participating actively in the disease progression. The present review aims at giving an overview of the implication of the lysosome in breast cancer, and at showing how subproteomics and the constantly refining MS-based proteomic techniques may help in making breast cancer research progress, and thus, hopefully, in improving disease treatment. Copyright 2004 Wiley Periodicals, Inc.,Mass Spec Rev

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Year:  2004        PMID: 15290709     DOI: 10.1002/mas.20001

Source DB:  PubMed          Journal:  Mass Spectrom Rev        ISSN: 0277-7037            Impact factor:   10.946


  3 in total

1.  Amelogenin exons 8 and 9 encoded peptide enhances leucine rich amelogenin peptide mediated dental pulp repair.

Authors:  Yulei Huang; Michel Goldberg; Thuan Le; Ran Qiang; Douglas Warner; Halina Ewa Witkowska; Haichuan Liu; Li Zhu; Pamela Denbesten; Wu Li
Journal:  Cells Tissues Organs       Date:  2012-02-01       Impact factor: 2.481

2.  Classification of subcellular location by comparative proteomic analysis of native and density-shifted lysosomes.

Authors:  Maria Cecilia Della Valle; David E Sleat; Haiyan Zheng; Dirk F Moore; Michel Jadot; Peter Lobel
Journal:  Mol Cell Proteomics       Date:  2011-01-20       Impact factor: 5.911

3.  Comparison of functional proteomic analyses of human breast cancer cell lines T47D and MCF7.

Authors:  Juliette Adjo Aka; Juliette Adjo Aka; Sheng-Xiang Lin
Journal:  PLoS One       Date:  2012-02-24       Impact factor: 3.240

  3 in total

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