cervical intraepithelial neoplasia/hypoxia

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GreinarKlínískar rannsóknirEinkaleyfi

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Roles for hypoxia-regulated genes during cervical carcinogenesis: somatic evolution during the hypoxia-glycolysis-acidosis sequence.

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OBJECTIVE Malignant phenotypic traits are caused by microenvironmental selection pressures during carcinogenesis. Hypoxia can drive a tumor toward a more aggressive malignant phenotype. The objective was to better understand the role of the hypoxia-regulated genes in cervical

How does hypoxia inducible factor-1α participate in enhancing the glycolysis activity in cervical cancer?

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The objective of this study is to explore the role of hypoxia inducible factor-1 (HIF-1) in glycolysis activity and its relationship with malignant biologic behaviors of cervical cancer. Immunohistochemistry was performed to study the protein expression and distribution of HIF-1α and glucose

Expression of vascular endothelial growth factor and hypoxia inducible factor-1alpha in cervical neoplasia.

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Altered angiogenesis is an important phenotype of high-grade cervical lesions and invasive cervical carcinomas. Many researchers, including us, have shown that oncoproteins of human papillomavirus could enhance the vascular endothelial growth factor (VEGF) expression. We investigated the change in

Hypoxia inducible factor-1 mediates upregulation of urokinase-type plasminogen activator receptor gene transcription during hypoxia in cervical cancer cells.

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Hypoxia occurs during development of cervical cancer and is considered to correlate with its invasion. Hypoxia mediates tumor cells to have more invasive property in a variety of cancers. Urokinase plasminogen activator receptor (uPAR) which mediates invasion is considered to be induced by hypoxia.

Prognostic assessment of hypoxia and metabolic markers in cervical cancer using automated digital image analysis of immunohistochemistry.

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BACKGROUND Hypoxia inducible factor-1 alpha (HIF-1α), induced by tumor hypoxia, regulates tumor cell metabolism and metastasis by up-regulation of c-Met, carbonic anhydrase 9 (CA9) and glucose transporter 1 (GLUT1). The prognostic significance of hypoxia and metabolic markers is not clearly defined

HSP27 is commonly expressed in cervical intraepithelial lesions of Brazilian women.

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Heat shock proteins are molecular chaperones that may be constitutively present in cells protecting them from various stresses, such as extreme temperature, anoxia or chemical agents. Cervical cancer is the second most prevalent malignancy of women. In this study, we analyzed the expression of Hsp27

MicroRNA-143 regulates the proliferation and apoptosis of cervical cancer cells by targeting HIF-1α.

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OBJECTIVE To investigate the effects of miR-143 on proliferation and apoptosis of cervical cancer HeLa cells and its target hypoxia-inducible factor-1α (HIF-1α). METHODS The expression levels of miR-143 in 30 cases of normal cervical tissues, 30 cases of cervical intraepithelial neoplasia tissues,

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