Literature DB >> 22592457

Correlation of expression of hypoxia-related proteins with prognosis in oral squamous cell carcinoma patients.

A W Eckert1, M Kappler, J Schubert, H Taubert.   

Abstract

INTRODUCTION: Hypoxia plays a major role in tumor progression, therapy resistance and for prognosis of oral squamous cell carcinoma (OSCC). The crucial step as a response to hypoxia is the activation and stabilization of the alpha subunit of hypoxia inducible factor 1 (HIF-1α). HIF-1: HIF-1 regulates the expression of different genes to adapt the tumor cells to reduced oxygenation. The HIF-1 system is intrinsic regulated by von Hippel-Lindau protein (pVHL). Main downstream proteins are the glucose transporter 1 (GLUT-1), carbonic anhydrase IX (CAIX), and vascular endothelial growth factor (VEGF). For therapeutical stratification in OSCC, it is important to understand the mechanism caused by hypoxic stress and to comprehend the resulting adaptive process in cancer cells. Therefore, an overview of HIF-1α-depending protein expression, focussed on the expression of GLUT-1, CAIX, and VEGF and their prognostic significance in OSCC is given.
CONCLUSION: Several unique roles of hypoxic pathway in the context of tumor progression are described in this review. As a consequence, a marker panel is proposed to allow a more individualized prognosis in OSCC patients. This marker panel should include beside HIF-1α, pVHL, and GLUT-1.

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Year:  2012        PMID: 22592457     DOI: 10.1007/s10006-012-0335-8

Source DB:  PubMed          Journal:  Oral Maxillofac Surg        ISSN: 1865-1550


  82 in total

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2.  Molecular marker expression in oral and oropharyngeal squamous cell carcinoma.

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4.  Carbonic anhydrase IX expression is associated with tumor progression and a poor prognosis of lung adenocarcinoma.

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Journal:  Lung Cancer       Date:  2006-10-09       Impact factor: 5.705

5.  GLUT-1 staining of squamous cell carcinomas of the uterine cervix identifies a novel element of invasion.

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Review 6.  Hypoxia-mediated biological control.

Authors:  Jessica Cassavaugh; Karen M Lounsbury
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7.  Coexpression of hypoxia-inducible factor-1α and glucose transporter-1 is associated with poor prognosis in oral squamous cell carcinoma patients.

Authors:  Alexander W Eckert; Matthias H W Lautner; Andreas Schütze; Helge Taubert; Johannes Schubert; Udo Bilkenroth
Journal:  Histopathology       Date:  2011-03-25       Impact factor: 5.087

8.  Hypoxic induction of HIF-1alpha and VEGF expression in head and neck squamous cell carcinoma lines is mediated by stress activated protein kinases.

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Journal:  Oral Oncol       Date:  2002-04       Impact factor: 5.337

9.  Endogenous hypoxia markers: case not proven!

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  23 in total

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2.  Prognostic significance of monocarboxylate transporter expression in oral cavity tumors.

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4.  Paraoxonase-2 (PON2) protects oral squamous cell cancer cells against irradiation-induced apoptosis.

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5.  Evaluation of Nonpeptidic Ligand Conjugates for SPECT Imaging of Hypoxic and Carbonic Anhydrase IX-Expressing Cancers.

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6.  Glucose transporters 1, 3, 6, and 10 are expressed in gastric cancer and glucose transporter 3 is associated with UICC stage and survival.

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Review 7.  Carbonic anhydrase IX as an imaging and therapeutic target for tumors and metastases.

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8.  Significance of HIF-1α Expression and LOXL-2 Localization in Progression of Oral Squamous Cell Carcinoma.

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9.  Gene and protein expression of glucose transporter 1 and glucose transporter 3 in human laryngeal cancer-the relationship with regulatory hypoxia-inducible factor-1α expression, tumor invasiveness, and patient prognosis.

Authors:  Katarzyna Starska; Ewa Forma; Paweł Jóźwiak; Magdalena Bryś; Iwona Lewy-Trenda; Ewa Brzezińska-Błaszczyk; Anna Krześlak
Journal:  Tumour Biol       Date:  2014-11-21

10.  WISP-1 a novel angiogenic regulator of the CCN family promotes oral squamous cell carcinoma angiogenesis through VEGF-A expression.

Authors:  Jing-Yuan Chuang; Po-Chun Chen; Ching-Wen Tsao; An-Chen Chang; Ming-Yu Lein; Ching-Chia Lin; Shih-Wei Wang; Chiao-Wen Lin; Chih-Hsin Tang
Journal:  Oncotarget       Date:  2015-02-28
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