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1.
NPJ Precis Oncol ; 2: 26, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-30480095

RESUMEN

Secretome of primary cultures is an accessible source of biological markers compared to more complex and less decipherable mixtures such as serum or plasma. The protonation state (PS) of secretome reflects the metabolism of cells and can be used for cancer early detection. Here, we demonstrate a superhydrophobic organic electrochemical device that measures PS in a drop of secretome derived from liquid biopsies. Using data from the sensor and principal component analysis (PCA), we developed algorithms able to efficiently discriminate tumour patients from non-tumour patients. We then validated the results using mass spectrometry and biochemical analysis of samples. For the 36 patients across three independent cohorts, the method identified tumour patients with high sensitivity and identification as high as 100% (no false positives) with declared subjects at-risk, for sporadic cancer onset, by intermediate values of PS. This assay could impact on cancer risk management, individual's diagnosis and/or help clarify risk in healthy populations.

2.
Oncogene ; 32(38): 4572-8, 2013 Sep 19.
Artículo en Inglés | MEDLINE | ID: mdl-23108393

RESUMEN

The serum- and glucocorticoid-regulated kinase (Sgk1) is essential for hormonal regulation of epithelial sodium channel-mediated sodium transport and is involved in the transduction of growth factor-dependent cell survival and proliferation signals. Growing evidence now points to Sgk1 as a key element in the development and/or progression of human cancer. To gain insight into the mechanisms through which Sgk1 regulates cell proliferation, we adopted a proteomic approach to identify up- or downregulated proteins after Sgk1-specific RNA silencing. Among several proteins, the abundance of which was found to be up- or downregulated upon Sgk1 silencing, we focused our attention of RAN-binding protein 1 (RANBP1), a major effector of the GTPase RAN. We report that Sgk1-dependent regulation of RANBP1 has functional consequences on both mitotic microtubule activity and taxol sensitivity of cancer cells.


Asunto(s)
Carcinoma/genética , Carcinoma/metabolismo , Neoplasias del Colon/genética , Neoplasias del Colon/metabolismo , Resistencia a Antineoplásicos/genética , Proteínas Inmediatas-Precoces/metabolismo , Proteínas Nucleares/genética , Proteínas Serina-Treonina Quinasas/metabolismo , Transcripción Genética , Apoptosis/efectos de los fármacos , Apoptosis/genética , Línea Celular Tumoral , Regulación Neoplásica de la Expresión Génica , Humanos , Paclitaxel/farmacología , Fosforilación , Proteómica , Interferencia de ARN , Factor de Transcripción Sp1/metabolismo
3.
Front Biosci (Landmark Ed) ; 18(2): 564-71, 2013 01 01.
Artículo en Inglés | MEDLINE | ID: mdl-23276942

RESUMEN

Brugada Syndrome (BS) is a polygenic inherited cardiac disease characterized by life-threatening arrhythmias and high incidence of sudden death. In this study, two-dimensional gel electrophoresis (2D-PAGE) coupled to mass spectrometry (LC-MS/MS) was used to investigate specific changes in the plasma proteome of BS patients and family members sharing the same gene mutation (SCN5AQ1118X), with the aim to identify novel disease biomarkers. Our data demonstrate that the levels of several proteins were significantly altered in BS patients compared with controls. In particular, apolipoprotein E, prothrombin, vitronectin, complement-factor H, vitamin-D-binding protein, voltage-dependent anion-selective channel protein 3 and clusterin were considerably increased in plasma sample of BS patients, whereas alpha-1-antitrypsin, fibrinogen and angiotensinogen were considerably decreased; moreover, post-translational modifications of antithrombin-III were detected in all affected individuals. On the light of these results, we hypothesize that these proteins might be considered as potential markers for the identification of disease status in BS.


Asunto(s)
Biomarcadores/sangre , Síndrome de Brugada/genética , Proteoma/análisis , Antitrombina III/metabolismo , Apolipoproteínas E/genética , Síndrome de Brugada/sangre , Electrocardiografía , Electroforesis en Gel Bidimensional , Femenino , Humanos , Masculino , Canal de Sodio Activado por Voltaje NAV1.5/genética , Linaje , Procesamiento Proteico-Postraduccional , Proteómica/métodos , Protrombina/genética , Espectrometría de Masas en Tándem , alfa 1-Antitripsina/genética
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