Identification of the TP53-induced glycolysis and apoptosis regulator in various stages of colorectal cancer patients
The TP53-induced glycolysis and apoptosis regulator (TIGAR) is a p53 target gene known to regulate glycolysis by acting as fructose bis-phosphatase (FBPase) and modulate reactive oxygen species. TIGAR expression has been implicated in oncogenesis and progression of several human cancers. However, TI...
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Published in | Oncology reports Vol. 35; no. 3; pp. 1281 - 1286 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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D.A. Spandidos
01.03.2016
Spandidos Publications Spandidos Publications UK Ltd |
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Abstract | The TP53-induced glycolysis and apoptosis regulator (TIGAR) is a p53 target gene known to regulate glycolysis by acting as fructose bis-phosphatase (FBPase) and modulate reactive oxygen species. TIGAR expression has been implicated in oncogenesis and progression of several human cancers. However, TIGAR expression is not known in various stages of colorectal cancer (CRC). There is an increase in the colorectal cancer incidence in Saudi Arabia. We sought to analyze TIGAR expression in this ethnic group. The aim of this study was to investigate the TIGAR expression in colorectal cancer (CRC) patients from Saudi Arabia. Tissue microarray (TMA) was constructed from 22 matched colorectal tumor tissues and adjacent normal tissues. TIGAR expression was examined in TMA slide using immunohistochemistry. TIGAR mRNA was determined in 14 matched tumor tissue and adjacent normal tissue. TIGAR protein expression was also examined in CRC tumor tissues and cell lines. Statistical analyses (t-test) were applied to evaluate the significance of TIGAR expression. TIGAR mRNA level was upregulated significantly in stage II (p<0.01) and stage III (p<0.05) when compared to adjacent normal tissue. Immunohistochemical studies revealed that TIGAR expression was increased in colorectal cancer. Strong TIGAR positive staining was found in 68% (15/22) of the tumor samples with nuclear localization. TIGAR staining was found to be significantly increased in early stage (stage I and II) CRC (p<0.05) and late stage (stage III and IV) CRC (p<0.01). TIGAR protein was also found to be highly expressed in stage II and III colorectal cancer tissues and CRC cell lines. These findings indicate that TIGAR is highly expressed at the mRNA and protein levels in colorectal cancer with prominent nuclear localization. TIGAR expression may be used as a bio-marker for detection of colorectal cancer and can be used as a target for developing therapeutics for the treatment of colorectal cancer. |
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AbstractList | The TP53-induced glycolysis and apoptosis regulator (TIGAR) is a p53 target gene known to regulate glycolysis by acting as fructose bis-phosphatase (FBPase) and modulate reactive oxygen species. TIGAR expression has been implicated in oncogenesis and progression of several human cancers. However, TIGAR expression is not known in various stages of colorectal cancer (CRC). There is an increase in the colorectal cancer incidence in Saudi Arabia. We sought to analyze TIGAR expression in this ethnic group. The aim of this study was to investigate the TIGAR expression in colorectal cancer (CRC) patients from Saudi Arabia. Tissue microarray (TMA) was constructed from 22 matched colorectal tumor tissues and adjacent normal tissues. TIGAR expression was examined in TMA slide using immunohistochemistry. TIGAR mRNA was determined in 14 matched tumor tissue and adjacent normal tissue. TIGAR protein expression was also examined in CRC tumor tissues and cell lines. Statistical analyses (t-test) were applied to evaluate the significance of TIGAR expression. TIGAR mRNA level was upregulated significantly in stage II (p<0.01) and stage III (p<0.05) when compared to adjacent normal tissue. Immunohistochemical studies revealed that TIGAR expression was increased in colorectal cancer. Strong TIGAR positive staining was found in 68% (15/22) of the tumor samples with nuclear localization. TIGAR staining was found to be significantly increased in early stage (stage I and II) CRC (p<0.05) and late stage (stage III and IV) CRC (p<0.01). TIGAR protein was also found to be highly expressed in stage II and III colorectal cancer tissues and CRC cell lines. These findings indicate that TIGAR is highly expressed at the mRNA and protein levels in colorectal cancer with prominent nuclear localization. TIGAR expression may be used as a bio-marker for detection of colorectal cancer and can be used as a target for developing therapeutics for the treatment of colorectal cancer. |
Audience | Academic |
Author | KATTAN, WAEL AL AHMAD, REHAN AL-KHAYAL, KHAYAL VAALI-MOHAMMED, MANSOOR-ALI AL-OBEED, OMAR ABDULLA, MAHA ZUBAIDI, AHMAD ALSHEIKH, ABDULMALIK |
AuthorAffiliation | 1 Colorectal Research Chair, College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia 3 Department of Surgery, College of Medicine, Al-Faisal University, Riyadh, Kingdom of Saudi Arabia 2 Department of Pathology, King Khalid University Hospital, Riyadh, Kingdom of Saudi Arabia |
AuthorAffiliation_xml | – name: 2 Department of Pathology, King Khalid University Hospital, Riyadh, Kingdom of Saudi Arabia – name: 1 Colorectal Research Chair, College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia – name: 3 Department of Surgery, College of Medicine, Al-Faisal University, Riyadh, Kingdom of Saudi Arabia |
Author_xml | – sequence: 1 givenname: KHAYAL surname: AL-KHAYAL fullname: AL-KHAYAL, KHAYAL organization: Colorectal Research Chair, College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia – sequence: 2 givenname: MAHA surname: ABDULLA fullname: ABDULLA, MAHA organization: Colorectal Research Chair, College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia – sequence: 3 givenname: OMAR surname: AL-OBEED fullname: AL-OBEED, OMAR organization: Colorectal Research Chair, College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia – sequence: 4 givenname: WAEL AL surname: KATTAN fullname: KATTAN, WAEL AL organization: Department of Surgery, College of Medicine, Al-Faisal University, Riyadh, Kingdom of Saudi Arabia – sequence: 5 givenname: AHMAD surname: ZUBAIDI fullname: ZUBAIDI, AHMAD organization: Colorectal Research Chair, College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia – sequence: 6 givenname: MANSOOR-ALI surname: VAALI-MOHAMMED fullname: VAALI-MOHAMMED, MANSOOR-ALI organization: Colorectal Research Chair, College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia – sequence: 7 givenname: ABDULMALIK surname: ALSHEIKH fullname: ALSHEIKH, ABDULMALIK organization: Department of Pathology, King Khalid University Hospital, Riyadh, Kingdom of Saudi Arabia – sequence: 8 givenname: REHAN surname: AHMAD fullname: AHMAD, REHAN organization: Colorectal Research Chair, College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia |
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SubjectTerms | Adult Aged Aged, 80 and over Antioxidants Apoptosis Apoptosis - genetics Apoptosis Regulatory Proteins Biomarkers Biosynthesis Cell cycle Cell growth Cell Line, Tumor Cell Transformation, Neoplastic - genetics Colorectal cancer Colorectal Neoplasms - genetics Colorectal Neoplasms - pathology Development and progression DNA damage Female Gene expression Gene Expression Regulation, Neoplastic Genetic aspects Health aspects HT29 Cells Humans immunohistochemistry Intracellular Signaling Peptides and Proteins - biosynthesis Intracellular Signaling Peptides and Proteins - genetics Male Medical prognosis Metabolism Metabolites Metastasis Middle Aged Neoplasm Staging Patients Proteins Reactive Oxygen Species - metabolism RNA, Messenger - biosynthesis Senescence Studies Tissue Array Analysis tissue microarray TP53-induced glycolysis and apoptosis regulator Tumor proteins Tumor Suppressor Protein p53 - genetics Tumor Suppressor Protein p53 - metabolism |
Title | Identification of the TP53-induced glycolysis and apoptosis regulator in various stages of colorectal cancer patients |
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