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Expression of HIF-1α in medullary thyroid cancer identifies a subgroup with poor prognosis.

Authors :
Lodewijk L
van Diest P
van der Groep P
Ter Hoeve N
Schepers A
Morreau J
Bonenkamp J
van Engen-van Grunsven A
Kruijff S
van Hemel B
Links T
Nieveen van Dijkum E
van Eeden S
Valk G
Borel Rinkes I
Vriens M
Source :
Oncotarget [Oncotarget] 2017 Apr 25; Vol. 8 (17), pp. 28650-28659.
Publication Year :
2017

Abstract

Background: Medullary thyroid cancer (MTC) comprises only 4% of all thyroid cancers and originates from the parafollicular C-cells. HIF-1α expression has been implied as an indicator of worse prognosis in various solid tumors. However, whether expression of HIF-1α is a prognosticator in MTC remained unclear. Our aim was to evaluate the prognostic value of HIF-1α in patients with MTC.<br />Methods: All patients with MTC who were operated on between 1988 and 2014 in five tertiary referral centers in The Netherlands were included. A tissue microarray was constructed in which 111 primary tumors could be analyzed for expression of HIF-1α, CAIX, Glut-1, VEGF and CD31 and correlated with clinicopathologic variables and survival.<br />Results: The mean age of patients was 46.3 years (SD 15.6), 59 (53.2%) were male. Of the 111 primary tumors, 49 (44.1%) were HIF-1α negative and 62 (55.9%) were HIF-1α positive. Positive HIF-1α expression was an independent negative indicator for progression free survival (PFS) in multivariate cox regression analysis (HR 3.1; 95% CI 1.3 - 7.3). Five-years survival decreased from 94.0% to 65.9% for the HIF-1α positive group (p=0.007). Even within the group of patients with TNM-stage IV disease, HIF-1α positivity was associated with a worse prognosis, shown by a decrease in 5-years survival of 88.0% to 49.3% (p=0.020).<br />Conclusion: Expression of HIF-1α is strongly correlated with adverse prognosis of MTC. This could open up new ways for targeted systemic therapy of MTC.

Details

Language :
English
ISSN :
1949-2553
Volume :
8
Issue :
17
Database :
MEDLINE
Journal :
Oncotarget
Publication Type :
Academic Journal
Accession number :
28404916
Full Text :
https://doi.org/10.18632/oncotarget.15622