<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(7)</volume><submitter>Ito T</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The prognosis of angiosarcoma is poor and a novel treatment option for the disease is desired. The aim of this study was to investigate the prognostic significance of Forkhead box M1 (FOXM1), a transcription factor that regulates cell-cycle progression and various crucial processes in tumor progression, and its potential as a new therapeutic target.&lt;h4>Methods&lt;/h4>We investigated 125 angiosarcoma clinical samples (94 primary lesions and 31 metastatic lesions in 94 patients) and a human angiosarcoma cell line (HAMON) using immunohistochemical staining and molecular biological approaches. FOXM1 expression in angiosarcoma samples was also compared with that in Kaposi's sarcomas (n = 13), epithelioid hemangioendotheliomas (n = 13) and benign hemangiomas (n = 10).&lt;h4>Results&lt;/h4>Patients with FOXM1-overexpressing angiosarcoma had significantly shorter survival (both for disease-specific survival [DSS] and event-free survival [EFS]) than other patients (5-year DSS, 23.5% vs. 47.1%, P = 0.013; and 5-year EFS, 5.5% vs. 28.7%, P = 0.004). FOXM1 overexpression was also an independent prognostic factor for both DSS and EFS in Cox multivariate analyses (hazard ratio [HR] 2.84, 95% confidence interval [CI] 1.10-5.81, P = 0.039; and HR 4.16, 95%CI 2.03-8.67, P = 0.0001, respectively). FOXM1 inhibition using both small interfering RNA and a specific inhibitor (thiostrepton) suppressed cell proliferation of the angiosarcoma cell line. Furthermore, FOXM1 inhibition improved the chemosensitivity to docetaxel in vitro.&lt;h4>Conclusions&lt;/h4>FOXM1 inhibition may be a potential therapeutic option for angiosarcoma.</pubmed_abstract><journal>Journal of Cancer</journal><pagination>823-30</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4860799</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Prognostic Significance of Forkhead Box M1 (FOXM1) Expression and Antitumor Effect of FOXM1 Inhibition in Angiosarcoma.</pubmed_title><pmcid>PMC4860799</pmcid><pubmed_authors>Kohashi K</pubmed_authors><pubmed_authors>Iwasaki T</pubmed_authors><pubmed_authors>Ito T</pubmed_authors><pubmed_authors>Maekawa A</pubmed_authors><pubmed_authors>Abe R</pubmed_authors><pubmed_authors>Hoshina D</pubmed_authors><pubmed_authors>Furue M</pubmed_authors><pubmed_authors>Yamada Y</pubmed_authors><pubmed_authors>Oda Y</pubmed_authors><pubmed_authors>Kuda M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prognostic Significance of Forkhead Box M1 (FOXM1) Expression and Antitumor Effect of FOXM1 Inhibition in Angiosarcoma.</name><description>&lt;h4>Background&lt;/h4>The prognosis of angiosarcoma is poor and a novel treatment option for the disease is desired. The aim of this study was to investigate the prognostic significance of Forkhead box M1 (FOXM1), a transcription factor that regulates cell-cycle progression and various crucial processes in tumor progression, and its potential as a new therapeutic target.&lt;h4>Methods&lt;/h4>We investigated 125 angiosarcoma clinical samples (94 primary lesions and 31 metastatic lesions in 94 patients) and a human angiosarcoma cell line (HAMON) using immunohistochemical staining and molecular biological approaches. FOXM1 expression in angiosarcoma samples was also compared with that in Kaposi's sarcomas (n = 13), epithelioid hemangioendotheliomas (n = 13) and benign hemangiomas (n = 10).&lt;h4>Results&lt;/h4>Patients with FOXM1-overexpressing angiosarcoma had significantly shorter survival (both for disease-specific survival [DSS] and event-free survival [EFS]) than other patients (5-year DSS, 23.5% vs. 47.1%, P = 0.013; and 5-year EFS, 5.5% vs. 28.7%, P = 0.004). FOXM1 overexpression was also an independent prognostic factor for both DSS and EFS in Cox multivariate analyses (hazard ratio [HR] 2.84, 95% confidence interval [CI] 1.10-5.81, P = 0.039; and HR 4.16, 95%CI 2.03-8.67, P = 0.0001, respectively). FOXM1 inhibition using both small interfering RNA and a specific inhibitor (thiostrepton) suppressed cell proliferation of the angiosarcoma cell line. Furthermore, FOXM1 inhibition improved the chemosensitivity to docetaxel in vitro.&lt;h4>Conclusions&lt;/h4>FOXM1 inhibition may be a potential therapeutic option for angiosarcoma.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016</publication><modification>2025-04-19T23:19:15.093Z</modification><creation>2019-03-27T02:13:18Z</creation></dates><accession>S-EPMC4860799</accession><cross_references><pubmed>27162541</pubmed><doi>10.7150/jca.14461</doi></cross_references></HashMap>