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1.
Cytokine Growth Factor Rev ; 31: 37-48, 2016 10.
Artículo en Inglés | MEDLINE | ID: mdl-27079372

RESUMEN

Adipose tissue is a highly vascularized endocrine organ, and its secretion profiles may vary with obesity. Adiponectin is secreted by adipocytes that make up adipose tissue. Worldwide, obesity has been designated a serious health problem among women and is associated with a variety of metabolic disorders and an increased risk of developing cancer of the cervix, ovaries, uterus (uterine/endometrial), and breast. In this review, the potential link between obesity and female-specific malignancies is comprehensively presented by discussing significant features of the intriguing and complex molecule, adiponectin, with a focus on recent findings highlighting its molecular mechanism of action in female-specific carcinogenesis.


Asunto(s)
Adiponectina/metabolismo , Carcinogénesis/metabolismo , Obesidad/complicaciones , Obesidad/metabolismo , Femenino , Humanos , Neoplasias/etiología , Neoplasias/metabolismo , Receptores de Adiponectina/metabolismo
2.
Tumour Biol ; 37(1): 97-104, 2016 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-26537581

RESUMEN

Colon and pancreatic cancers have high mortality rates due to early metastasis prior to the onset of symptoms. Screening tests for colorectal cancer are invasive and expensive. No effective screening is available for pancreatic cancer. Identification of biomarkers for early detection in both of these cancers is being extensively researched. MicroRNAs (miRNA) are small non-coding molecule biomarkers that regulate cancers. Measurement of miRNAs in pancreatic fluid or blood could be a preferred non-invasive screening method. The regulation of colon and pancreatic cancers by miRNA is complex. miRNA play a central role in inflammation, invasiveness, and tumor progression in these two cancers, as well as regulation of the NF-κB pathway. miRNA's evolving role in screening is also reviewed.


Asunto(s)
Biomarcadores de Tumor/metabolismo , Neoplasias del Colon/metabolismo , Regulación Neoplásica de la Expresión Génica , MicroARNs/metabolismo , FN-kappa B/metabolismo , Neoplasias Pancreáticas/metabolismo , Neoplasias del Colon/genética , Neoplasias del Colon/terapia , Progresión de la Enfermedad , Perfilación de la Expresión Génica , Humanos , Inflamación , Invasividad Neoplásica , Neoplasias Pancreáticas/genética , Neoplasias Pancreáticas/terapia , Resultado del Tratamiento
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