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1.
Int J Mol Sci ; 25(17)2024 Sep 03.
Artículo en Inglés | MEDLINE | ID: mdl-39273514

RESUMEN

The early detection of tumors is one of the key factors in increasing overall survival in cancer patients. A wide range of cancers still do not have a system of early diagnosis; therefore, the development of new non-invasive tools in this line is essential. Accordingly, the objective of our work was to develop a non-invasive screening method for the early detection of various carcinomas in plasma using a panel that combines two markers using RT-qPCR. A retrospective case-control study was conducted to develop a cancer screening test based on the detection of stromal and epithelial biomarkers (COL1A2 and KRT19) in plasma. The expression of biomarkers was evaluated using multiplex quantitative PCR applied to 47 cases with non-metastatic tumors and 13 control participants. For both biomarkers, a cut-off value was stablished using Youden's J index through ROC curve analysis and areas under the curve (AUC) were calculated. The plasma mRNA expression level of both biomarkers was significantly higher in diseased versus healthy patients. Moreover, ROC curve analysis showed an AUC value of 0.897 for the combined model. This model also resulted in a cutoff value of 0.664, as well as a sensitivity of 83% and a specificity of 84.6%. These results suggest that the plasma expression levels of COL1A2 and KRT19 could a have potential role in detecting various types of cancer at the early stages. The combined analysis of both stromal and epithelial biomarkers would provide a non-invasive screening method that would allow us to differentiate patients with an active neoplastic process.


Asunto(s)
Biomarcadores de Tumor , Colágeno Tipo I , Queratina-19 , Reacción en Cadena de la Polimerasa Multiplex , Neoplasias , ARN Mensajero , Humanos , Queratina-19/genética , Queratina-19/sangre , Biopsia Líquida/métodos , Masculino , Biomarcadores de Tumor/sangre , Biomarcadores de Tumor/genética , Femenino , Colágeno Tipo I/genética , Colágeno Tipo I/sangre , ARN Mensajero/genética , ARN Mensajero/sangre , Persona de Mediana Edad , Neoplasias/genética , Neoplasias/diagnóstico , Neoplasias/sangre , Anciano , Reacción en Cadena de la Polimerasa Multiplex/métodos , Estudios de Casos y Controles , Adulto , Estudios Retrospectivos , Curva ROC , Detección Precoz del Cáncer/métodos
2.
Int J Mol Sci ; 24(4)2023 Feb 10.
Artículo en Inglés | MEDLINE | ID: mdl-36834987

RESUMEN

Tumor-derived extracellular vesicles (TD-EVs) have active roles as cancer hallmark enablers. EVs RNA of epithelial and stromal cells carry information that facilitates the communication processes that contribute to oncological progression, so the objective of this work was to validate by RT-PCR the presence of epithelial (KRT19; CEA) and stromal (COL1A2; COL11A1) markers in RNA of plasmatic EVs in healthy and diverse-malignancy patients for the development of a non-invasive cancer diagnosis system using liquid biopsy. Ten asymptomatic controls and 20 cancer patients were included in the study, and results showed that the isolated plasmatic EVs by scanning transmission electron microscopy (STEM) andBiomedical Research Institute A Coruña nanoparticle tracking analysis (NTA) contained most exosome structures with also a considerable percentage of microvesicles. No differences were found in concentration and size distribution between the two cohorts of patients, but significant gene expression in epithelial and mesenchymal markers between healthy donors and patients with active oncological disease was shown. Results of quantitative RT-PCR are solid and reliable for KRT19, COL1A2, and COL11A1, so the analysis of RNA extracted from TD-EVs could be a correct approach to develop a diagnostic tool in oncological processes.


Asunto(s)
Biomarcadores de Tumor , Transición Epitelial-Mesenquimal , Vesículas Extracelulares , Humanos , Biomarcadores de Tumor/genética , Biomarcadores de Tumor/metabolismo , Exosomas , Vesículas Extracelulares/genética , Vesículas Extracelulares/metabolismo , Procesos Neoplásicos , ARN/metabolismo , Transición Epitelial-Mesenquimal/genética
3.
Int J Impot Res ; 35(3): 286-305, 2023 May.
Artículo en Inglés | MEDLINE | ID: mdl-35501394

RESUMEN

Immunohistological patterns of density and distribution of neural tissue in the human penis, including the prepuce, are not fully characterized, and effects of circumcision (partial or total removal of the penile prepuce) on penile sexual sensation are controversial. This study analyzed extra- and intracavernosal innervation patterns on the main penile axes using formalin-fixed, paraffin-embedded human adult and fetal penile tissues, single- and double-staining immunohistochemistry and a variety of neural and non-neural markers, with a special emphasis on the prepuce and potential sexual effects of circumcision. Immunohistochemical profiles of neural structures were determined and the most detailed immunohistological characterizations to date of preputial nerve supply are provided. The penile prepuce has a highly organized, dense, afferent innervation pattern that is manifest early in fetal development. Autonomically, it receives noradrenergic sympathetic and nitrergic parasympathetic innervation. Cholinergic nerves are also present. We observed cutaneous and subcutaneous neural density distribution biases across our specimens towards the ventral prepuce, including a region corresponding in the adult anatomical position (penis erect) to the distal third of the ventral penile aspect. We also describe a concept of innervation gradients across the longitudinal and transverse penile axes. Results are discussed in relation to the specialized literature. An argument is made that neuroanatomic substrates underlying unusual permanent penile sensory disturbances post-circumcision are related to heightened neural levels in the distal third of the ventral penile aspect, which could potentially be compromised by deep incisions during circumcision.


Asunto(s)
Circuncisión Masculina , Pene , Masculino , Adulto , Humanos , Pene/cirugía , Prepucio/cirugía , Circuncisión Masculina/métodos , Sensación , Conducta Sexual
4.
PLoS One ; 7(10): e45434, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-23056203

RESUMEN

The quest for therapeutic applications of obestatin involves, as a first step, the determination of its 3D solution structure and the relationship between this structure and the biological activity of obestatin. On this basis, we have employed a combination of circular dichroism (CD), nuclear magnetic resonance (NMR) spectroscopy, and modeling techniques to determine the solution structure of human obestatin (1). Other analogues, including human non-amidated obestatin (2) and the fragment peptides (6-23)-obestatin (3), (11-23)-obestatin (4), and (16-23)-obestatin (5) have also been scrutinized. These studies have been performed in a micellar environment to mimic the cell membrane (sodium dodecyl sulfate, SDS). Furthermore, structural-activity relationship studies have been performed by assessing the in vitro proliferative capabilities of these peptides in the human retinal pigmented epithelial cell line ARPE-19 (ERK1/2 and Akt phosphorylation, Ki67 expression, and cellular proliferation). Our findings emphasize the importance of both the primary structure (composition and size) and particular segments of the obestatin molecule that posses significant α-helical characteristics. Additionally, details of a species-specific role for obestatin have also been hypothesized by comparing human and mouse obestatins (1 and 6, respectively) at both the structural and bioactivity levels.


Asunto(s)
Membrana Celular/química , Ghrelina/química , Espectroscopía de Resonancia Magnética/métodos , Micelas , Secuencia de Aminoácidos , Animales , Línea Celular , Proliferación Celular/efectos de los fármacos , Dicroismo Circular/métodos , Células Epiteliales/citología , Células Epiteliales/efectos de los fármacos , Células Epiteliales/metabolismo , Ghrelina/farmacología , Humanos , Inmunohistoquímica , Antígeno Ki-67/metabolismo , Ratones , Modelos Moleculares , Datos de Secuencia Molecular , Conformación Proteica , Estructura Secundaria de Proteína , Receptores Acoplados a Proteínas G/metabolismo , Epitelio Pigmentado de la Retina/citología , Homología de Secuencia de Aminoácido , Dodecil Sulfato de Sodio/química , Soluciones/química , Relación Estructura-Actividad
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