Particulate-fraction and soluble-fraction proteins from examples of breast carcinoma, Hodgkin's lympboma, and colon adenocarcinoma and their corresponding normal tissues were resolved on sodium dodecyl sulfate-polyacrylamide gels. The Coomassie blue-stained protein patterns were quantitated using a
Multi-biomarker pattern for tumor identification and prognosis
✍ Scribed by Sara Rodríguez-Enríquez; Silvia Cecilia Pacheco-Velázquez; Juan Carlos Gallardo-Pérez; Alvaro Marín-Hernández; José Luis Aguilar-Ponce; Erika Ruiz-García; Luz María RuizGodoy-Rivera; Abelardo Meneses-García; Rafael Moreno-Sánchez
- Book ID
- 102876273
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 624 KB
- Volume
- 112
- Category
- Article
- ISSN
- 0730-2312
No coin nor oath required. For personal study only.
✦ Synopsis
In last decades, the basic, clinical, and translational research efforts have been directed to the identification of standard biomarkers associated with the degree of malignancy. There is an increasingly public health concern for earlier detection of cancer development at stages in which successful treatments can be achieved. To meet this urgent clinical demand, early stage cancer biomarkers supported by reliable and robust experimental data that can be readily applicable in the clinical practice, are required. In the current standard protocols, when one or two of the canonical proliferating index biomarkers are analyzed, contradictory results are frequently reached leading to incorrect cancer diagnostic and unsuccessful therapies. Therefore, the identification of other cellular characteristics or signatures present in the tumor cells either alone or in combination with the well-established proliferation markers emerge as an alternative strategy in the improvement of cancer diagnosis and treatment. Because it is well known that several pathways and processes are altered in tumor cells, the concept of ''single marker'' in cancer results incorrect. Therefore, this review aims to analyze and discuss the proposal that the molecular profile of different genes or proteins in different altered tumor pathways must be established to provide a better global clinical pattern for cancer detection and prognosis.
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