Hif-1α Inhibitors Could Successfully Inhibit the Progression of Differentiated Thyroid Cancer in Vitro

Hypoxia-inducible factor (HIF)-1α plays an important role in cancer progression. In various cancers, including thyroid cancer, overexpression of HIF-1α is related to poor prognosis or treatment response. However, few studies have investigated the role of HIF-1α inhibition in thyroid cancer progressi...

Full description

Bibliographic Details
Main Authors: Min-Hee Kim, Tae Hyeong Lee, Jin Soo Lee, Dong-Jun Lim, Peter Chang-Whan Lee
Format: Article
Language:English
Published: MDPI AG 2020-08-01
Series:Pharmaceuticals
Subjects:
Online Access:https://www.mdpi.com/1424-8247/13/9/208
_version_ 1797555939246604288
author Min-Hee Kim
Tae Hyeong Lee
Jin Soo Lee
Dong-Jun Lim
Peter Chang-Whan Lee
author_facet Min-Hee Kim
Tae Hyeong Lee
Jin Soo Lee
Dong-Jun Lim
Peter Chang-Whan Lee
author_sort Min-Hee Kim
collection DOAJ
description Hypoxia-inducible factor (HIF)-1α plays an important role in cancer progression. In various cancers, including thyroid cancer, overexpression of HIF-1α is related to poor prognosis or treatment response. However, few studies have investigated the role of HIF-1α inhibition in thyroid cancer progression. We evaluated the utility of the HIF-1α inhibitor IDF-11774 in vitro utilizing two thyroid cancer cell lines, K1 and BCPAP. Both cell lines were tested to elucidate the effects of IDF-11774 on cell proliferation and migration using soft agar and invasion assays. Here, we found that a reduction of HIF-1α expression in BCPAP cells was observed after treatment with IDF-11774 in a dose-dependent manner. Moreover, cell proliferation, migration, and anchorage-independent growth were effectively inhibited by IDF-11774 in BCPAP cells but not in K1 cells. Additionally, invasion of BCPAP but not K1 cells was controlled with IDF-11774 in a dose-dependent manner. Our findings suggest that promoting the degradation of HIF-1α could be a strategy to manage progression and that HIF-1α inhibitors are potent drugs for thyroid cancer treatment.
first_indexed 2024-03-10T16:54:44Z
format Article
id doaj.art-3781a8503d734001bc0678bbe05bf5d8
institution Directory Open Access Journal
issn 1424-8247
language English
last_indexed 2024-03-10T16:54:44Z
publishDate 2020-08-01
publisher MDPI AG
record_format Article
series Pharmaceuticals
spelling doaj.art-3781a8503d734001bc0678bbe05bf5d82023-11-20T11:10:05ZengMDPI AGPharmaceuticals1424-82472020-08-0113920810.3390/ph13090208Hif-1α Inhibitors Could Successfully Inhibit the Progression of Differentiated Thyroid Cancer in VitroMin-Hee Kim0Tae Hyeong Lee1Jin Soo Lee2Dong-Jun Lim3Peter Chang-Whan Lee4Division of Endocrinology and Metabolism, Department of Internal Medicine, Eunpyeong St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul 03312, KoreaDepartment of Biomedical Sciences, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, KoreaDivision of Endocrinology and Metabolism, Department of Internal Medicine, Eunpyeong St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul 03312, KoreaDivision of Endocrinology and Metabolism, Department of Internal Medicine, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul 06591, KoreaDepartment of Biomedical Sciences, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, KoreaHypoxia-inducible factor (HIF)-1α plays an important role in cancer progression. In various cancers, including thyroid cancer, overexpression of HIF-1α is related to poor prognosis or treatment response. However, few studies have investigated the role of HIF-1α inhibition in thyroid cancer progression. We evaluated the utility of the HIF-1α inhibitor IDF-11774 in vitro utilizing two thyroid cancer cell lines, K1 and BCPAP. Both cell lines were tested to elucidate the effects of IDF-11774 on cell proliferation and migration using soft agar and invasion assays. Here, we found that a reduction of HIF-1α expression in BCPAP cells was observed after treatment with IDF-11774 in a dose-dependent manner. Moreover, cell proliferation, migration, and anchorage-independent growth were effectively inhibited by IDF-11774 in BCPAP cells but not in K1 cells. Additionally, invasion of BCPAP but not K1 cells was controlled with IDF-11774 in a dose-dependent manner. Our findings suggest that promoting the degradation of HIF-1α could be a strategy to manage progression and that HIF-1α inhibitors are potent drugs for thyroid cancer treatment.https://www.mdpi.com/1424-8247/13/9/208HIF-1αIDF-11774thyroid cancer
spellingShingle Min-Hee Kim
Tae Hyeong Lee
Jin Soo Lee
Dong-Jun Lim
Peter Chang-Whan Lee
Hif-1α Inhibitors Could Successfully Inhibit the Progression of Differentiated Thyroid Cancer in Vitro
Pharmaceuticals
HIF-1α
IDF-11774
thyroid cancer
title Hif-1α Inhibitors Could Successfully Inhibit the Progression of Differentiated Thyroid Cancer in Vitro
title_full Hif-1α Inhibitors Could Successfully Inhibit the Progression of Differentiated Thyroid Cancer in Vitro
title_fullStr Hif-1α Inhibitors Could Successfully Inhibit the Progression of Differentiated Thyroid Cancer in Vitro
title_full_unstemmed Hif-1α Inhibitors Could Successfully Inhibit the Progression of Differentiated Thyroid Cancer in Vitro
title_short Hif-1α Inhibitors Could Successfully Inhibit the Progression of Differentiated Thyroid Cancer in Vitro
title_sort hif 1α inhibitors could successfully inhibit the progression of differentiated thyroid cancer in vitro
topic HIF-1α
IDF-11774
thyroid cancer
url https://www.mdpi.com/1424-8247/13/9/208
work_keys_str_mv AT minheekim hif1ainhibitorscouldsuccessfullyinhibittheprogressionofdifferentiatedthyroidcancerinvitro
AT taehyeonglee hif1ainhibitorscouldsuccessfullyinhibittheprogressionofdifferentiatedthyroidcancerinvitro
AT jinsoolee hif1ainhibitorscouldsuccessfullyinhibittheprogressionofdifferentiatedthyroidcancerinvitro
AT dongjunlim hif1ainhibitorscouldsuccessfullyinhibittheprogressionofdifferentiatedthyroidcancerinvitro
AT peterchangwhanlee hif1ainhibitorscouldsuccessfullyinhibittheprogressionofdifferentiatedthyroidcancerinvitro