Regulation of HIF-1-Alpha, miR-200, and Markers of Cancer Stem Cells by CDF Under Hypoxic Condition

Abstract

Prostate Cancer (PCa) is the most commonly diagnosed cancer in men and is the second leading cause of cancer death in the USA (1). Most PCa patients are treatable, but the patients usually die due to drug resistance and metastatic disease. Thus, there is a dire need for the development of novel strategies by which drug resistance and metastatic disease could be controlled with novel agents with better treatment outcome. Hypoxia is one of the fundamental biological phenomena that are intricately associated with the development and aggressiveness of a variety of solid tumors including PCa. Hypoxia-inducible factors (HIF) function as a master transcription factor, which regulates hypoxia responsive genes and have been recognized to play critical roles in tumor invasion, metastasis, and chemo-radiation resistance, and contributes to increased cell proliferation, survival, angiogenesis and metastasis (2, 3). Therefore, tumor hypoxia with deregulated expression of HIF and its biological consequence lead to poor prognosis of patients diagnosed with solid tumors, resulting in higher mortality, suggesting that understanding of the molecular relationship of hypoxia with other cellular features of tumor aggressiveness would be invaluable for developing newer targeted therapy for solid tumors. It has been well recognized that cancer stem cells (CSCs) and epithelial-to-mesenchymal transition (EMT) phenotypic cells are associated with therapeutic resistance and contributes to aggressive tumor growth, invasion, metastasis, and are believed to be the cause of tumor recurrence (4). Emerging evidence suggest that hypoxia and HIF pathway enhance the phenotypes and functions of CSC and EMT (5-9), contributing to tumor aggressiveness, which could also be due to deregulation of microRNAs (miRNAs).

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Document Details

Document Type
Technical Report
Publication Date
Apr 01, 2012
Accession Number
ADA562451

Entities

People

  • Bin Bao

Organizations

  • Wayne State University

Tags

DTIC Thesaurus Topics

  • Abstracts
  • Analogs
  • Biomedical Research
  • Cell Movement
  • Cell Physiological Processes
  • Cells
  • Complexometric Indicators
  • Confocal Microscopy
  • Diseases And Disorders
  • Drug Resistance
  • Endothelial Cells
  • Gene Expression
  • Neoplasms
  • Prostate Cancer
  • Proteins
  • Stem Cells
  • Wound Healing

Fields of Study

  • Biology
  • Chemistry

Readers

  • Molecular Biology and Genetics
  • Prostate Cancer Biology.

Technology Areas

  • Biotechnology