Literature DB >> 11344232

Inhibin/activin betaB-subunit expression in pheochromocytomas favors benign diagnosis.

K Salmenkivi1, J Arola, R Voutilainen, V Ilvesmäki, C Haglund, A I Kahri, P Heikkilä, J Liu.   

Abstract

Malignancy of pheochromocytomas is difficult to estimate on the basis of histopathological features. Good prognostic markers are not available. In our search for new markers to differentiate malignant pheochromocytomas from benign ones we tested the value of inhibin/activin subunit expression. Inhibins are heterodimeric glycoproteins consisting of an alpha-subunit and either a betaA- or a betaB-subunit. Activins are composed of beta-subunits only. Immunohistochemically inhibin/activin betaB-subunit was strongly positive in the normal adrenal medulla, but the cortex was negative. A striking difference was found in inhibin/activin betaB expression between benign and malignant pheochromocytomas. The majority of benign adrenal tumors (27 of 30) showed strong or moderate immunoreactivity, whereas all seven malignant tumors were negative or only weakly positive for inhibin/activin betaB-subunit. The percentage of positively staining cells varied greatly in extraadrenal pheochromocytomas and in those benign tumors that showed over 5 mitoses/10 high power fields, necrosis, or capsular or vascular invasion, here called borderline tumors. Inhibin/activin betaB messenger ribonucleic acid was also found in pheochromocytomas. However, no significant differences in messenger ribonucleic acid levels were found in various types of tumors. Weak immunohistochemical positivity for inhibin/activin betaA-subunit was detected in the adrenal cortex, but the medulla and most of the pheochromocytomas were negative. Our data show that inhibin/activin betaB-subunit is expressed in normal adrenal medullary cells. Strong staining is found in most benign adrenal pheochromocytomas, whereas malignant tumors are almost negative. This suggests that loss of inhibin/activin betaB-subunit expression in pheochromocytomas may be used as an indicator of malignant potential.

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Year:  2001        PMID: 11344232     DOI: 10.1210/jcem.86.5.7446

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  6 in total

1.  A logistic regression model for predicting malignant pheochromocytomas.

Authors:  Baohua Gao; Yanxia Sun; Zhongguo Liu; Fanwei Meng; Benkang Shi; Yuqiang Liu; Zhishun Xu
Journal:  J Cancer Res Clin Oncol       Date:  2007-11-13       Impact factor: 4.553

2.  Pheochromocytoma: an uncommon presentation of an asymptomatic and biochemically silent adrenal incidentaloma.

Authors:  Sunil Kumar Kota; Siva Krishna Kota; Sandip Panda; Kirtikumar D Modi
Journal:  Malays J Med Sci       Date:  2012-04

Review 3.  Molecular genetic alterations in adrenal and extra-adrenal pheochromocytomas and paragangliomas.

Authors:  Hilde Dannenberg; Paul Komminoth; Winand N M Dinjens; Ernst Jan M Speel; Ronald R de Krijger
Journal:  Endocr Pathol       Date:  2003       Impact factor: 3.943

4.  Inhibin/activin expression in human and rodent liver: subunits α and βB as new players in human hepatocellular carcinoma?

Authors:  K Frost; K Seir; A Lackner; M Grusch; B Grasl-Kraupp; R Schulte-Hermann; C Rodgarkia-Dara
Journal:  Br J Cancer       Date:  2011-03-15       Impact factor: 7.640

5.  Pheochromocytoma with inferior vena cava thrombosis: An unusual association.

Authors:  Sunil K Kota; Siva K Kota; Sruti Jammula; Lalit K Meher; Kirtikumar D Modi
Journal:  J Cardiovasc Dis Res       Date:  2012-04

6.  MiR-148a functions to suppress metastasis and serves as a prognostic indicator in triple-negative breast cancer.

Authors:  Xin Xu; Yun Zhang; Jeff Jasper; Erik Lykken; Peter B Alexander; Geoffrey J Markowitz; Donald P McDonnell; Qi-Jing Li; Xiao-Fan Wang
Journal:  Oncotarget       Date:  2016-04-12
  6 in total

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