Prognostic significance of pituitary tumour-transforming gene-binding factor (PBF) expression in papillary thyroid carcinoma

Summary Background Pituitary tumour‐transforming gene (PTTG)‐binding factor (PBF), originally known as PTTG1 interacting protein (PTTG1IP), has been found to be significantly increased in well‐differentiated thyroid cancer and independently associated with early tumour recurrence. Objective To asses...

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Published inClinical endocrinology (Oxford) Vol. 78; no. 2; pp. 303 - 309
Main Authors Hsueh, Chuen, Lin, Jen-Der, Chang, Yu-Sun, Hsueh, Swei, Chao, Tzu-Chieh, Yu, Jau-Song, Jung, Shih-Ming, Tseng, Ngan-Ming, Sun, Jui-Hung, Kuo, Shau-Yun, Ueng, Shir-Hwa
Format Journal Article
LanguageEnglish
Published Oxford Blackwell Publishing Ltd 01.02.2013
Blackwell
Wiley Subscription Services, Inc
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ISSN0300-0664
1365-2265
1365-2265
DOI10.1111/cen.12007

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Abstract Summary Background Pituitary tumour‐transforming gene (PTTG)‐binding factor (PBF), originally known as PTTG1 interacting protein (PTTG1IP), has been found to be significantly increased in well‐differentiated thyroid cancer and independently associated with early tumour recurrence. Objective To assess the prognostic significance of PBF expression in a large cohort of papillary thyroid carcinoma (PTC) patients with a long‐term follow‐up. Design and patients Retrospective analysis of PBF expression in PTC cases at different stages and correlate it with various clinicopathological parameters and patient survival. Subjects included 153 patients who received a thyroid operation for PTC at Chang Gung Memorial Hospital between 1991 and 2000. All patients had a complete follow‐up till the end of 2010. Measurements Immunohistochemical study for PBF expression on tissue sections from tumour specimens. Bond automated machine (Leica Microsystems, Germany) with a polyclonal rabbit anti‐PBF antibody (LifeSpan BioSciences, LS‐C118942, Seattle, WA, USA) was used. SPSS 13.0 for Windows (SPSS Inc, Chicago, IL, USA) was used for all statistical analyses. Results High PBF expression was significantly correlated with age (P = 0·0298), distant metastases at diagnosis (P = 0·0139), tumour multicentricity (P = 0·0035), TNM stage (P = 0·0103), locoregional recurrence (P = 0·0410) and disease‐specific mortality (P = 0·0064). The expression level of PBF was significantly correlated with disease‐specific survival (P = 0·0065). Cox regression analysis showed that age, tumour size and PBF expression were independent prognostic indicators (P = 0·0097, P = 0·0021 and P = 0·0179). Conclusion PBF expression may be a promising biomarker for prognostic and therapeutic purpose. More large‐scale studies are needed to clarify its potential usefulness.
AbstractList Pituitary tumour-transforming gene (PTTG)-binding factor (PBF), originally known as PTTG1 interacting protein (PTTG1IP), has been found to be significantly increased in well-differentiated thyroid cancer and independently associated with early tumour recurrence. To assess the prognostic significance of PBF expression in a large cohort of papillary thyroid carcinoma (PTC) patients with a long-term follow-up. Retrospective analysis of PBF expression in PTC cases at different stages and correlate it with various clinicopathological parameters and patient survival. Subjects included 153 patients who received a thyroid operation for PTC at Chang Gung Memorial Hospital between 1991 and 2000. All patients had a complete follow-up till the end of 2010. Immunohistochemical study for PBF expression on tissue sections from tumour specimens. Bond automated machine (Leica Microsystems, Germany) with a polyclonal rabbit anti-PBF antibody (LifeSpan BioSciences, LS-C118942, Seattle, WA, USA) was used. SPSS 13.0 for Windows (SPSS Inc, Chicago, IL, USA) was used for all statistical analyses. High PBF expression was significantly correlated with age (P=0.0298), distant metastases at diagnosis (P=0.0139), tumour multicentricity (P=0.0035), TNM stage (P=0.0103), locoregional recurrence (P=0.0410) and disease-specific mortality (P=0.0064). The expression level of PBF was significantly correlated with disease-specific survival (P=0.0065). Cox regression analysis showed that age, tumour size and PBF expression were independent prognostic indicators (P=0.0097, P=0.0021 and P =0.0179). PBF expression may be a promising biomarker for prognostic and therapeutic purpose. More large-scale studies are needed to clarify its potential usefulness.
Summary Background Pituitary tumour‐transforming gene (PTTG)‐binding factor (PBF), originally known as PTTG1 interacting protein (PTTG1IP), has been found to be significantly increased in well‐differentiated thyroid cancer and independently associated with early tumour recurrence. Objective To assess the prognostic significance of PBF expression in a large cohort of papillary thyroid carcinoma (PTC) patients with a long‐term follow‐up. Design and patients Retrospective analysis of PBF expression in PTC cases at different stages and correlate it with various clinicopathological parameters and patient survival. Subjects included 153 patients who received a thyroid operation for PTC at Chang Gung Memorial Hospital between 1991 and 2000. All patients had a complete follow‐up till the end of 2010. Measurements Immunohistochemical study for PBF expression on tissue sections from tumour specimens. Bond automated machine (Leica Microsystems, Germany) with a polyclonal rabbit anti‐PBF antibody (LifeSpan BioSciences, LS‐C118942, Seattle, WA, USA) was used. SPSS 13.0 for Windows (SPSS Inc, Chicago, IL, USA) was used for all statistical analyses. Results High PBF expression was significantly correlated with age (P = 0·0298), distant metastases at diagnosis (P = 0·0139), tumour multicentricity (P = 0·0035), TNM stage (P = 0·0103), locoregional recurrence (P = 0·0410) and disease‐specific mortality (P = 0·0064). The expression level of PBF was significantly correlated with disease‐specific survival (P = 0·0065). Cox regression analysis showed that age, tumour size and PBF expression were independent prognostic indicators (P = 0·0097, P = 0·0021 and P = 0·0179). Conclusion PBF expression may be a promising biomarker for prognostic and therapeutic purpose. More large‐scale studies are needed to clarify its potential usefulness.
Pituitary tumour-transforming gene (PTTG)-binding factor (PBF), originally known as PTTG1 interacting protein (PTTG1IP), has been found to be significantly increased in well-differentiated thyroid cancer and independently associated with early tumour recurrence. To assess the prognostic significance of PBF expression in a large cohort of papillary thyroid carcinoma (PTC) patients with a long-term follow-up. Retrospective analysis of PBF expression in PTC cases at different stages and correlate it with various clinicopathological parameters and patient survival. Subjects included 153 patients who received a thyroid operation for PTC at Chang Gung Memorial Hospital between 1991 and 2000. All patients had a complete follow-up till the end of 2010. Immunohistochemical study for PBF expression on tissue sections from tumour specimens. Bond automated machine (Leica Microsystems, Germany) with a polyclonal rabbit anti-PBF antibody (LifeSpan BioSciences, LS-C118942, Seattle, WA, USA) was used. SPSS 13.0 for Windows (SPSS Inc, Chicago, IL, USA) was used for all statistical analyses. High PBF expression was significantly correlated with age (P = 0·0298), distant metastases at diagnosis (P = 0·0139), tumour multicentricity (P = 0·0035), TNM stage (P = 0·0103), locoregional recurrence (P = 0·0410) and disease-specific mortality (P = 0·0064). The expression level of PBF was significantly correlated with disease-specific survival (P = 0·0065). Cox regression analysis showed that age, tumour size and PBF expression were independent prognostic indicators (P = 0·0097, P = 0·0021 and P = 0·0179). PBF expression may be a promising biomarker for prognostic and therapeutic purpose. More large-scale studies are needed to clarify its potential usefulness.
Summary Background Pituitary tumour-transforming gene (PTTG)-binding factor (PBF), originally known as PTTG1 interacting protein (PTTG1IP), has been found to be significantly increased in well-differentiated thyroid cancer and independently associated with early tumour recurrence. Objective To assess the prognostic significance of PBF expression in a large cohort of papillary thyroid carcinoma (PTC) patients with a long-term follow-up. Design and patients Retrospective analysis of PBF expression in PTC cases at different stages and correlate it with various clinicopathological parameters and patient survival. Subjects included 153 patients who received a thyroid operation for PTC at Chang Gung Memorial Hospital between 1991 and 2000. All patients had a complete follow-up till the end of 2010. Measurements Immunohistochemical study for PBF expression on tissue sections from tumour specimens. Bond automated machine (Leica Microsystems, Germany) with a polyclonal rabbit anti-PBF antibody (LifeSpan BioSciences, LS-C118942, Seattle, WA,USA) was used. SPSS 13.0 for Windows (SPSS Inc, Chicago, IL,USA) was used for all statistical analyses. Results High PBF expression was significantly correlated with age (P = 0·0298), distant metastases at diagnosis (P = 0·0139), tumour multicentricity (P = 0·0035), TNM stage (P = 0·0103), locoregional recurrence (P = 0·0410) and disease-specific mortality (P = 0·0064). The expression level of PBF was significantly correlated with disease-specific survival (P = 0·0065). Cox regression analysis showed that age, tumour size and PBF expression were independent prognostic indicators (P = 0·0097, P = 0·0021 and P = 0·0179). Conclusion PBF expression may be a promising biomarker for prognostic and therapeutic purpose. More large-scale studies are needed to clarify its potential usefulness. [PUBLICATION ABSTRACT]
Pituitary tumour-transforming gene (PTTG)-binding factor (PBF), originally known as PTTG1 interacting protein (PTTG1IP), has been found to be significantly increased in well-differentiated thyroid cancer and independently associated with early tumour recurrence.BACKGROUNDPituitary tumour-transforming gene (PTTG)-binding factor (PBF), originally known as PTTG1 interacting protein (PTTG1IP), has been found to be significantly increased in well-differentiated thyroid cancer and independently associated with early tumour recurrence.To assess the prognostic significance of PBF expression in a large cohort of papillary thyroid carcinoma (PTC) patients with a long-term follow-up.OBJECTIVETo assess the prognostic significance of PBF expression in a large cohort of papillary thyroid carcinoma (PTC) patients with a long-term follow-up.Retrospective analysis of PBF expression in PTC cases at different stages and correlate it with various clinicopathological parameters and patient survival. Subjects included 153 patients who received a thyroid operation for PTC at Chang Gung Memorial Hospital between 1991 and 2000. All patients had a complete follow-up till the end of 2010.DESIGN AND PATIENTSRetrospective analysis of PBF expression in PTC cases at different stages and correlate it with various clinicopathological parameters and patient survival. Subjects included 153 patients who received a thyroid operation for PTC at Chang Gung Memorial Hospital between 1991 and 2000. All patients had a complete follow-up till the end of 2010.Immunohistochemical study for PBF expression on tissue sections from tumour specimens. Bond automated machine (Leica Microsystems, Germany) with a polyclonal rabbit anti-PBF antibody (LifeSpan BioSciences, LS-C118942, Seattle, WA, USA) was used. SPSS 13.0 for Windows (SPSS Inc, Chicago, IL, USA) was used for all statistical analyses.MEASUREMENTSImmunohistochemical study for PBF expression on tissue sections from tumour specimens. Bond automated machine (Leica Microsystems, Germany) with a polyclonal rabbit anti-PBF antibody (LifeSpan BioSciences, LS-C118942, Seattle, WA, USA) was used. SPSS 13.0 for Windows (SPSS Inc, Chicago, IL, USA) was used for all statistical analyses.High PBF expression was significantly correlated with age (P = 0·0298), distant metastases at diagnosis (P = 0·0139), tumour multicentricity (P = 0·0035), TNM stage (P = 0·0103), locoregional recurrence (P = 0·0410) and disease-specific mortality (P = 0·0064). The expression level of PBF was significantly correlated with disease-specific survival (P = 0·0065). Cox regression analysis showed that age, tumour size and PBF expression were independent prognostic indicators (P = 0·0097, P = 0·0021 and P = 0·0179).RESULTSHigh PBF expression was significantly correlated with age (P = 0·0298), distant metastases at diagnosis (P = 0·0139), tumour multicentricity (P = 0·0035), TNM stage (P = 0·0103), locoregional recurrence (P = 0·0410) and disease-specific mortality (P = 0·0064). The expression level of PBF was significantly correlated with disease-specific survival (P = 0·0065). Cox regression analysis showed that age, tumour size and PBF expression were independent prognostic indicators (P = 0·0097, P = 0·0021 and P = 0·0179).PBF expression may be a promising biomarker for prognostic and therapeutic purpose. More large-scale studies are needed to clarify its potential usefulness.CONCLUSIONPBF expression may be a promising biomarker for prognostic and therapeutic purpose. More large-scale studies are needed to clarify its potential usefulness.
Author Chang, Yu-Sun
Sun, Jui-Hung
Hsueh, Chuen
Chao, Tzu-Chieh
Yu, Jau-Song
Kuo, Shau-Yun
Lin, Jen-Der
Jung, Shih-Ming
Hsueh, Swei
Tseng, Ngan-Ming
Ueng, Shir-Hwa
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Issue 2
Keywords Endocrinopathy
Binding
Endocrine gland
Prognosis
Thyroid diseases
Pituitary gland
Malignant tumor
Gene expression
Papillary thyroid carcinoma
Endocrinology
Cancer
Language English
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2012 Blackwell Publishing Ltd.
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  text: February 2013
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PublicationTitle Clinical endocrinology (Oxford)
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References Mazzaferri, E.L. & Kloos, R.T. (2001) Clinical review 128: current approaches to primary therapy for papillary and follicular thyroid cancer. Journal of Clinical Endocrinology and Metabolism, 86, 1447-1463.
Read, M.L., Lewy, G.D., Fong, J.C. et al. (2011) Proto-oncogene PBF/PTTG1IP regulates thyroid cell growth and represses radioiodide treatment. Cancer Research, 71, 6153-6164.
Yaspo, M.L., Aaltonen, J., Horelli-Kuitunen, N. et al. (1998) Cloning of a novel human putative type Ia integral membrane protein mapping to 21q22.3. Genomics, 49, 133-136.
McCabe, C.J., Boelaert, K., Tannahill, L.A. et al. (2002) Vascular endothelial growth factor (VEGF), its receptor KDR and pituitary tumor transforming gene in pituitary tumors. The Journal of Clinical Endocrinology and Metabolism, 87, 4238-4244.
Bork, P., Doerks, T., Springer, T.A. et al. (1999) Domains in plexins: links to integrins and transcription factors. Trends in Biochemical Sciences, 24, 261-263.
Lin, J.D., Chao, T.C., Hsueh, C. et al. (2009) High recurrent rate of multi-centric papillary thyroid carcinoma. Annals of Surgical Oncology, 16, 2609-2616.
Heaney, A.P., Nelson, V., Fernando, M. et al. (2001) Transforming events in thyroid tumorigenesis and their association with follicular lesions. Journal of Clinical Endocrinology and Metabolism, 86, 5025-5032.
Smith, V.E., Read, M.L., Turnell, A.S. et al. (2009) A novel mechanism of sodium iodide symporter repression in differentiated thyroid cancer. Journal of Cell Science, 122, 3393-3402.
Vlotides, G., Eigler, T. & Melmed, S. (2007) Pituitary tumor-transforming gene: physiology and implications for tumorigenesis. Endocrine Reviews, 28, 165-186.
Lin, J.D., Hsueh, C. & Chao, T.C. (2009) Early recurrence papillary and follicular thyroid carcinoma predicts a worse outcome. Thyroid, 19, 1053-1058.
Xing, M. (2007) BRAF mutation in papillary thyroid cancer: pathogenic role, molecular bases, and clinical implications. Endocrine Reviews, 28, 742-762.
Zou, H., McGarry, T.J., Bernal, T. et al. (1999) Identification of a vertebrate sister-chromatid separation inhibitor involved in transformation and tumorigenesis. Science, 285, 418-422.
Kirkegaard, T., Edwards, J., Tovey, S. et al. (2006) Observer variation in immunohistochemical analysis of protein expression, time for a change? Histopathology, 48, 787-794.
Watkins, R.J., Read, M.L., Smith, V.E. et al. (2010) Pituitary tumor transforming gene binding factor: a new gene in breast cancer. Cancer Research, 70, 3739-3749.
Boelaert, K., McCabe, C.J., Tannahill, L.A. et al. (2003) Pituitary tumor transforming gene and fibroblast growth factor-2 expression: potential prognostic indicators in differentiated thyroid cancer. Journal of Clinical Endocrinology and Metabolism, 88, 2341-2347.
Kim, D.S., Franklyn, J.A., Stratford, A.L. et al. (2006) Pituitary tumor-transforming gene regulates multiple downstream angiogenic genes in thyroid cancer. Journal of Clinical Endocrinology and Metabolism, 91, 1119-1128.
Davies, L. & Welch, H.G. (2006) Increasing incidence of thyroid cancer in the United States, 1973-2002. Journal of the American Medical Association, 295, 2164-2167.
Chien, W. & Pei, L. (2000) A novel binding factor facilitates nuclear translocation and transcriptional activation function of the pituitary tumor-transforming gene product. Journal of Biological Chemistry, 275, 19422-19427.
Zhang, X, Horwitz, G.A., Prezant, T.R. et al. (1999b) Structure, expression, and function of human pituitary tumor-transforming gene (PTTG). Molecular Endocrinology 13, 156-166.
Pei, L. & Melmed, S. (1997) Isolation and characterization of a pituitary tumor-transforming gene (PTTG). Molecular Endocrinology, 11, 433-441.
McCabe, C.J., Khaira, J.S., Boelaert, K. et al. (2003) Expression of pituitary tumour transforming gene (PTTG) and fibroblast growth factor-2 (FGF-2) in human pituitary adenomas: relationships to clinical tumour behaviour. Clincal Endocrinology (Oxford), 58, 141-150.
Saez, C., Martinez-Brocca, M.A., Castilla, C. et al. (2006) Prognostic significance of human pituitary tumor-transforming gene immunohistochemical expression in differentiated thyroid cancer. Journal of Clinical Endocrinology and Metabolism, 91, 1404-1409.
Ishikawa, H., Heaney, A.P., Yu, R. et al. (2001) Human pituitary tumor-transforming gene induces angiogenesis. Journal of Clinical Endocrinology and Metabolism, 86, 867-874.
Hay, I.D., Thompson, G.B., Grant, C.S. et al. (2002) Papillary thyroid carcinoma managed at the Mayo Clinic during six decades (1940-1999): temporal trends in initial therapy and long-term outcome in 2444 consecutively treated patients. World Journal of Surgery, 26, 879-885.
Boelaert, K., Smith, V.E., Stratford, A.L. et al. (2007) PTTG and PBF repress the human sodium iodide symporter. Oncogene, 26, 4344-4356.
Stratford, A.L., Boelaert, K., Tannahill, L.A. et al. (2005) Pituitary tumor transforming gene binding factor: a novel transforming gene in thyroid tumorigenesis. Journal of Clinical Endocrinology and Metabolism, 90, 4341-4349.
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References_xml – reference: Yaspo, M.L., Aaltonen, J., Horelli-Kuitunen, N. et al. (1998) Cloning of a novel human putative type Ia integral membrane protein mapping to 21q22.3. Genomics, 49, 133-136.
– reference: Smith, V.E., Read, M.L., Turnell, A.S. et al. (2009) A novel mechanism of sodium iodide symporter repression in differentiated thyroid cancer. Journal of Cell Science, 122, 3393-3402.
– reference: Zhang, X, Horwitz, G.A., Prezant, T.R. et al. (1999b) Structure, expression, and function of human pituitary tumor-transforming gene (PTTG). Molecular Endocrinology 13, 156-166.
– reference: Watkins, R.J., Read, M.L., Smith, V.E. et al. (2010) Pituitary tumor transforming gene binding factor: a new gene in breast cancer. Cancer Research, 70, 3739-3749.
– reference: Xing, M. (2007) BRAF mutation in papillary thyroid cancer: pathogenic role, molecular bases, and clinical implications. Endocrine Reviews, 28, 742-762.
– reference: Zou, H., McGarry, T.J., Bernal, T. et al. (1999) Identification of a vertebrate sister-chromatid separation inhibitor involved in transformation and tumorigenesis. Science, 285, 418-422.
– reference: Hay, I.D., Thompson, G.B., Grant, C.S. et al. (2002) Papillary thyroid carcinoma managed at the Mayo Clinic during six decades (1940-1999): temporal trends in initial therapy and long-term outcome in 2444 consecutively treated patients. World Journal of Surgery, 26, 879-885.
– reference: Kim, D.S., Franklyn, J.A., Stratford, A.L. et al. (2006) Pituitary tumor-transforming gene regulates multiple downstream angiogenic genes in thyroid cancer. Journal of Clinical Endocrinology and Metabolism, 91, 1119-1128.
– reference: Davies, L. & Welch, H.G. (2006) Increasing incidence of thyroid cancer in the United States, 1973-2002. Journal of the American Medical Association, 295, 2164-2167.
– reference: Lin, J.D., Hsueh, C. & Chao, T.C. (2009) Early recurrence papillary and follicular thyroid carcinoma predicts a worse outcome. Thyroid, 19, 1053-1058.
– reference: Bork, P., Doerks, T., Springer, T.A. et al. (1999) Domains in plexins: links to integrins and transcription factors. Trends in Biochemical Sciences, 24, 261-263.
– reference: Boelaert, K., Smith, V.E., Stratford, A.L. et al. (2007) PTTG and PBF repress the human sodium iodide symporter. Oncogene, 26, 4344-4356.
– reference: Ishikawa, H., Heaney, A.P., Yu, R. et al. (2001) Human pituitary tumor-transforming gene induces angiogenesis. Journal of Clinical Endocrinology and Metabolism, 86, 867-874.
– reference: Heaney, A.P., Nelson, V., Fernando, M. et al. (2001) Transforming events in thyroid tumorigenesis and their association with follicular lesions. Journal of Clinical Endocrinology and Metabolism, 86, 5025-5032.
– reference: Lin, J.D., Chao, T.C., Hsueh, C. et al. (2009) High recurrent rate of multi-centric papillary thyroid carcinoma. Annals of Surgical Oncology, 16, 2609-2616.
– reference: Mazzaferri, E.L. & Kloos, R.T. (2001) Clinical review 128: current approaches to primary therapy for papillary and follicular thyroid cancer. Journal of Clinical Endocrinology and Metabolism, 86, 1447-1463.
– reference: Pei, L. & Melmed, S. (1997) Isolation and characterization of a pituitary tumor-transforming gene (PTTG). Molecular Endocrinology, 11, 433-441.
– reference: McCabe, C.J., Boelaert, K., Tannahill, L.A. et al. (2002) Vascular endothelial growth factor (VEGF), its receptor KDR and pituitary tumor transforming gene in pituitary tumors. The Journal of Clinical Endocrinology and Metabolism, 87, 4238-4244.
– reference: Kirkegaard, T., Edwards, J., Tovey, S. et al. (2006) Observer variation in immunohistochemical analysis of protein expression, time for a change? Histopathology, 48, 787-794.
– reference: Vlotides, G., Eigler, T. & Melmed, S. (2007) Pituitary tumor-transforming gene: physiology and implications for tumorigenesis. Endocrine Reviews, 28, 165-186.
– reference: McCabe, C.J., Khaira, J.S., Boelaert, K. et al. (2003) Expression of pituitary tumour transforming gene (PTTG) and fibroblast growth factor-2 (FGF-2) in human pituitary adenomas: relationships to clinical tumour behaviour. Clincal Endocrinology (Oxford), 58, 141-150.
– reference: Read, M.L., Lewy, G.D., Fong, J.C. et al. (2011) Proto-oncogene PBF/PTTG1IP regulates thyroid cell growth and represses radioiodide treatment. Cancer Research, 71, 6153-6164.
– reference: Stratford, A.L., Boelaert, K., Tannahill, L.A. et al. (2005) Pituitary tumor transforming gene binding factor: a novel transforming gene in thyroid tumorigenesis. Journal of Clinical Endocrinology and Metabolism, 90, 4341-4349.
– reference: Chien, W. & Pei, L. (2000) A novel binding factor facilitates nuclear translocation and transcriptional activation function of the pituitary tumor-transforming gene product. Journal of Biological Chemistry, 275, 19422-19427.
– reference: Boelaert, K., McCabe, C.J., Tannahill, L.A. et al. (2003) Pituitary tumor transforming gene and fibroblast growth factor-2 expression: potential prognostic indicators in differentiated thyroid cancer. Journal of Clinical Endocrinology and Metabolism, 88, 2341-2347.
– reference: Saez, C., Martinez-Brocca, M.A., Castilla, C. et al. (2006) Prognostic significance of human pituitary tumor-transforming gene immunohistochemical expression in differentiated thyroid cancer. Journal of Clinical Endocrinology and Metabolism, 91, 1404-1409.
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Snippet Summary Background Pituitary tumour‐transforming gene (PTTG)‐binding factor (PBF), originally known as PTTG1 interacting protein (PTTG1IP), has been found to...
Pituitary tumour-transforming gene (PTTG)-binding factor (PBF), originally known as PTTG1 interacting protein (PTTG1IP), has been found to be significantly...
Summary Background Pituitary tumour-transforming gene (PTTG)-binding factor (PBF), originally known as PTTG1 interacting protein (PTTG1IP), has been found to...
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SubjectTerms Adolescent
Adult
Aged
Aged, 80 and over
Biological and medical sciences
Carcinoma, Papillary - metabolism
Carcinoma, Papillary - surgery
Endocrinopathies
Female
Fundamental and applied biological sciences. Psychology
Gene Expression Regulation, Neoplastic - physiology
Humans
Male
Malignant tumors
Medical sciences
Membrane Proteins - genetics
Membrane Proteins - metabolism
Middle Aged
Non tumoral diseases. Target tissue resistance. Benign neoplasms
Prognosis
Thyroid Neoplasms - metabolism
Thyroid Neoplasms - surgery
Thyroid. Thyroid axis (diseases)
Vertebrates: endocrinology
Young Adult
Title Prognostic significance of pituitary tumour-transforming gene-binding factor (PBF) expression in papillary thyroid carcinoma
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https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fcen.12007
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https://www.proquest.com/docview/1273300594
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