
pmid: 16552335
Hypoxia-inducible factor 1alpha (HIF-1alpha) has been universally detected in many types of cells and plays a key role in modulation of tumor-related genes. The purpose of this study was to explore the relationship between HIF-1alpha messenger RNA (mRNA) expression and biologic characteristics in pancreatic cancer, such as tumor angiogenesis, tumor cell proliferation, differentiation, apoptosis, and metastasis.Reverse transcriptase-polymerase chain reaction was used to detect HIF-1alpha mRNA expression. The expressions of survivin, proliferating cell nuclear antigen (PCNA), and CD34 proteins were measured immunohistochemically. The correlation between the expression levels of HIF-1alpha mRNA and survivin, PCNA, and CD34 were analyzed.There was very significant difference in the expression of HIF-1alpha between the pancreatic cancer tissue and adjacent normal tissue (P 0.05). There was significant difference in the expression of HIF-1alpha mRNA between Japanese Pancreatic Society stages I to II and stages III to IV (P < 0.05). The expression of HIF-1alpha mRNA was closely correlated with the expression of survivin, PCNA, and CD34 proteins.The expression level of HIF-1alpha mRNA is surmised to have a significant correlation with tumor angiogenesis, cell proliferation, apoptosis, and metastasis. Inhibition of HIF-1alpha may be an important and approachable therapeutic target for pancreatic cancer.
Reverse Transcriptase Polymerase Chain Reaction, Survivin, Antigens, CD34, Hypoxia-Inducible Factor 1, alpha Subunit, Survival Analysis, Inhibitor of Apoptosis Proteins, Neoplasm Proteins, Pancreatic Neoplasms, Proliferating Cell Nuclear Antigen, Humans, RNA, Messenger, RNA, Neoplasm, Microtubule-Associated Proteins, DNA Primers, Neoplasm Staging
Reverse Transcriptase Polymerase Chain Reaction, Survivin, Antigens, CD34, Hypoxia-Inducible Factor 1, alpha Subunit, Survival Analysis, Inhibitor of Apoptosis Proteins, Neoplasm Proteins, Pancreatic Neoplasms, Proliferating Cell Nuclear Antigen, Humans, RNA, Messenger, RNA, Neoplasm, Microtubule-Associated Proteins, DNA Primers, Neoplasm Staging
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